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  • 1
    Online Resource
    Online Resource
    Burlington :Elsevier Science & Technology,
    Keywords: Cell interaction. ; Connexins. ; Gap junctions (Cell biology). ; Electronic books.
    Description / Table of Contents: Since the first gap junction protein (connexin) was cloned over a decade ago, more than a dozen connexin genes have been cloned. Consequently, a wealth of information on the molecular basis of gap junctional communication has been accumulated. This book pays tribute to this exciting era in the history of cell communication research by documenting the great strides made in this field as a result of the merging of biophysics and molecular biology, two of the most powerful approaches to studying the molecular basis of membrane channel behavior. Twenty-eight comprehensive chapters, authored by internationally recognized leaders in the field, discuss the biophysical, physiological, and molecular characteristics of cell-to-cell communication via gap junctions. Key aspects of molecular structure, formation, gating, conductance, and permeability of vertebrate and invertebrate gap junction channels are highlighted. In addition, a number of chapters focus on recent discoveries that implicate connexin mutations and alterations of gap junctional communication in the pathogenesis of several diseases, including the X-linked Charcot Marie Tooth demyelinating disease, some forms of inherited sensorineural deafness, malignant transformation, cardiac malformations and arrhythmia, eye lens cataract, and Chagas' disease.
    Type of Medium: Online Resource
    Pages: 1 online resource (681 pages)
    Edition: 1st ed.
    ISBN: 9780080585208
    Series Statement: Issn Series ; v.Volume 49
    DDC: 571.6
    Language: English
    Note: Front Cover -- Gap Junctions: Molecular Basis of Cell Communication in Health and Disease -- Copyright Page -- Contents -- Contributors -- Preface -- Previous Volumes in Series -- Part I: Channel Structure, Assembly, and Degradation -- Chapter 1. Gap Junction Structure: New Structures and New Insights -- I. Overview of Gap Junction Structure -- II. The Constituent Proteins of Gap Junctions: Size and Topology Models of the Connexin Family -- III. Isolation and Purification of Gap Junctions -- IV. Molecular Structure of Gap Junctions Determined by X-Ray Diffraction and Electron Microscopy -- V. Concluding Remarks -- References -- Chapter 2. Degradation of Gap Junctions and Connexins -- I. Most Connexins Turn Over Rapidly -- II. Ubiquitin Pathway and Pathways of Protein Degradation -- III. Ubiquitin Dependence of Cx43 Degradation -- IV. Membrane Protein Degradation -- V. Lysosomal and Proteasomal Degradation of Cx43 -- VI. Phosphorylation and Regulation of Connexin Degradation -- VII. Heat-Induced Degradation of Cx43 -- VIII. Conclusion -- References -- Part II: Channel Forms, Permeability, and Conductance -- Chapter 3. Homotypic, Heterotypic, and Heteromeric Gap Junction Channels -- I. Introduction -- II. Homotypic hCx37 and rCx43 Gap Junction Channels -- III. Hetcrotypic hCx37-rCx43 Gap Junction Channels -- IV. Co-transfection of hCx37 and rCx43: Heteromcric Gap Junction Channels -- V. Why Would a Cell Bother with Heteromeric Gap Junction Channels? -- References -- Chapter 4. Heteromultimeric Gap Junction Channels and Cardiac Disease -- I. Introduction -- II. Gap Junctions: Structure and Nomenclature -- III. Endogenous Expression of Multiple Connexins in Various Tissues -- IV. Experimental Formation of Heteromultimeric Channels in Exogenous Systems -- V. Molecular Regions Involved in Assembly. , VI. Physiological Implications of Heteromultimeric Channel Formation -- VII. Conclusions and Future Directions -- Rcferences -- Chapter 5. Ion Permeation through Connexin Gap Junction Channels: Effects on Conductance and Selectivity -- I. Introduction -- II. Theories of Electrodiffusion -- III. Gap Junction Channel Conductance and Permeability -- IV. Summary -- References -- Chapter 6. Phosphorylation of Connexins: Consequences for Permeability, Conductance, and Kinetics of Gap Junction Channels -- I. Introduction -- II. Connexin43 -- III. Connexin40 and -45 -- IV. Connexin26 and -32 -- V. Concluding Remarks -- References -- Chapter 7. Intercellular Calcium Wave Communication via Gap Junction-Dependent and -Independent Mechanisms -- I. Introduction -- II. Two Routes for Intercellular Calcium Wave Propagation -- III. Some Features of Intercellular Ca2+ Waves Depend upon the Initiating Stimulus -- IV. Mechanisms for Intercellular Ca2+ Wave Propagation -- V. How Connexins Can Potentially Influence and Modulate the Propagation of Intercellular Ca2+ Waves -- VI. How the Extracellular Space May Influence Calcium Wave Propagation -- VII. Functional Roles of Intercellular Calcium Waves -- VIII. Prospects -- References -- Part III: Voltage Grating -- Chapter 8. Membrane Potential Dependence of Gap Junctions in Vertebrates -- I. Membrane Potential Dependence Is a Common Regulatory Mechanism among the Gap Junctions of Vertebrates -- II. One Mechanism of Vm Gating Resides in Each Hemichannel -- III. A Gating Model of Junctions with Combined Vj and Vm Dependence -- IV. Functional Role of Vm Dependence -- References -- Chapter 9. A Reexamination of Calcium Effects on Gap Junctions in Heart Myocytes -- I. Introduction -- II. The Calcium Hypothesis: Is Cell Coupling Regulated by Ca2+ Ions? -- III. Cytosolic Calcium Levels Correlating with Electrical Uncoupling. , IV. Conclusions -- References -- Part IV: Chemical Grating -- Chapter 10. Distinct Behaviors of Chemical- and Voltage- Sensitive Gates of Gap Junction Channel -- I. Introduction -- II. CO2-Induced Gating at Different Vj's -- III. Channel Reopening in Response to Reversal of Vj Polarity -- IV. Kinetics of Unitary Transitions -- V. Conclusions -- References -- Chapter 11. A Molecular Model for the Chemical Regulation of Connexin43 Channels: The "Ball-and-Chain" Hypothesis -- I. Introduction -- II. Connexin, the Gap Junction Protein -- III. pH Regulation of Connexins -- IV. Regulation of Cx43 by Protein Kinases -- V. Structure-Function Studies on pH Gating of Cx43 -- VI. The Particle-Receptor Concept Put in Practice: Peptide Block of pH Gating of Cx43 -- VII. Applicability of the Particle-Receptor Model to Gap Junction Regulation by Other Factors -- VIII. Cx43 Concatenants Do Not Function as the Simple Addition of Individual Subunits -- References -- Chapter 12. Mechanistic Differences between Chemical and Electrical Gating of Gap Junctions -- I. Introduction -- II. The Voltage Gating Mechanism -- III. Chemical Gating -- IV. Conclusions -- References -- Chapter 13. Behavior of Chemical- and Slow Voltage-Sensitive Gates of Connexin Channels: The "Cork" Gating Hypothesis -- I. Introduction -- II. Role of Cytosolic pH and Calcium in Channel Gating -- III. Potential Participation of Calmodulin in the Gating Mechanism -- IV. Connexin Domains Relevant to pH/Ca Gating -- V. Does Chemical Gating Require Connexin Cooperativity? -- VI. Is the Chemical Gate Voltage Sensitive? -- VII. Are There Intramolecular Interactions Relevant to Gating? -- VIII. The "Cork" Gating Model -- References -- Chapter 14. Molecular Determinants of Voltage Gating of Gap Junctions Formed by Connexin32 and 26 -- I. Introduction -- II. Vj-Dependent Gating. , III. Molecular Determinants of Vj Gating -- IV. Structural Implications -- V. Role of P87 Vj Gating -- VI. Conclusions -- References -- Chapter 15. Regulation of Connexin43 by Tyrosine Protein Kinases -- I. Introduction -- II. Regulation of Cx43 by Nonreceptor Tyrosine Kinases -- III. Regulation of Cx43 by Receptor Tyrosine Kinases -- IV. The "Particle-Receptor" Model of Phosphorylation- Induced Cx43 Channel Closure -- V. Summary and Future Directions -- References -- Chapter 16. Gating of Gap Junction Channels and Hemichannels in the Lens: A Role in Cataract? -- I. Introduction -- II. The Lens Circulation System and Role of Gap Junction Channels -- III. Molecular Composition and Functional Properties of Lens Gap Junction Channels -- IV. pH-Sensitive Gating of Lens Fiber Gap Junctions -- V. Fiber Cell Currents Reminiscent of Gap Junction Hemichannels -- VI. A Role for Gap Junction Channels and Hemichannels in Cataract? -- References -- Part V: Hemichannels -- Chapter 17. Biophysical Properties of Hemi-Gap-junctional Channels Expressed in Xenopus Oocytes -- I. Introduction -- II. Expression of Rat Cx46 in Xenopus Oocytes -- III. Single Channel Properties of Cx46 Hemichannels -- IV. Voltage Gating for Cx46 Hemichannels and Cx46 Hemichannels in Intercellular Channels -- V. Structure of Pore Lining Region of Cx46 Hemichannels Inferred from Cysteine Scanning Mutagenesis -- VI. Properties of Hemichannels Formed from Different Connexins -- VII. Heteromeric Association of Connexins Modifies Hemichannel Behavior -- VIII. Summary and Conclusions -- References -- Chapter 18. Properties of Connexin50 Hemichannels Expressed in Xenopus laevis Oocytes -- I. Introduction -- II. Experimental Procedures -- III. Electrophysiological Studies of Oocytes Expressing Connexin50 -- IV. Morphological Studies of Oocytes Expressing Connexin50 -- V. Conclusions -- References. , Part VI: Invertebrate Gap Junctions -- Chapter 19. Gap Junction Communication in Invertebrates: The lnnexin Gene Family -- I. Introductory Note -- II. Searching for Gap Junction Genes and Proteins in Invertebrates -- III. Innexins: Functional Connexin Analogues in Drosophila and C. elegans -- IV. Genetic Screens Unwittingly Identified Gap Junction Mutants -- V. Cloning Defined a New Gene Family with No Homology to the Vertebrate Connexins -- VI. Innexin Proteins -- VII. Functional Expression of Innexins in Heterologous Systems -- VIII. Distribution of Innexins -- IX. Innexins and the Study of Gap Junction Function in Invertebrates -- X. Looking Forward -- References -- Part VII: Diseases Based o n Defects of Cell Communication -- Chapter 20. Hereditary Human Diseases Caused by Connexin Mutations -- I. Introduction -- II. Mechanisms of Pathogenesis -- III. Mutations in Cx26 Lead to Nonsyndromic Deafness -- IV. Implications of Cx26 Mutations for Hearing -- V. Mutations in Cx31 Lead to Autosomal Dominant Erythrokeratodermia Variabilis or Deafness -- VI. Mutations in Cx32 Lead to an Inherited Peripheral Neuropathy -- VII. The Clinical Manifestations of CMTX -- VIII. Cx32 Expression in Schwann Cells and Pathogenesis of CMTX -- IX. Mutations in Cx43 Were Found in a Few Patients with Visceroatrial Heterotaxia -- X. Mutations in Cx46 and Cx50 Lead to Cataracts -- XI. Candidate Diseases for Other Connexins -- References -- Chapter 21. Trafficking and Targeting of Connexin32 Mutations to Gap Junctions in Charcot-Marie-Tooth X-Linked Disease -- I. Introduction -- II. Classification of Mutations in CMT-X -- III. Mechanisms Leading to the Intracellular Trapping of Mutant Protein -- IV. Gap Junction Targeting Determinants -- V. Mutations in Other Connexins and Disease -- VI. Concluding Remarks -- References. , Chapter 22. Molecular Basis of Deafness Due to Mutations in the Connexin26 Gene (GJB2).
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  • 2
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Biological transport, Active. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (444 pages)
    Edition: 1st ed.
    ISBN: 9780080488639
    Series Statement: Issn Series
    DDC: 572.3
    Language: English
    Note: Front Cover -- Mechanosensitive Ion Channels, Part A -- Copyright Page -- Contents -- Contributors -- Foreword -- Previous Volumes in Series -- Chapter 1: Structures of the Prokaryotic Mechanosensitive Channels MscL and MscS -- I. Overview -- II. Introduction -- III. Conductances of MscL and MscS: General Considerations -- IV. Structure Determination of MscL and MscS -- A. General Considerations in Membrane Protein Crystallography -- B. Crystallographic Analysis of MscL and MscS -- V. MscL and MscS Structures -- VI. The Permeation Pathway in MscL and MscS -- VII. Disulfide Bond Formation in MscL -- VIII. Concluding Remarks -- Acknowledgments -- References -- Chapter 2: 3.5 Billion Years of Mechanosensory Transduction: Structure and Function of Mechanosensitive Channels in Prokaryotes -- I. Overview -- II. Introduction -- III. Discovery, Mechanism, and Structure of MS Channels in Prokaryotes -- A. Historical Perspective -- B. Conductance, Selectivity, and Activation by Membrane Tension of Bacterial MS Channels -- C. Cloning of MscL and MscS of E. coli -- D. Molecular Identification of MS Channels in Archaea -- E. Molecular Structure of Prokaryotic MS Channels -- F. Bilayer Mechanism and Gating by Mechanical Force -- G. Spectroscopic Studies -- H. Structural Models of Gating in MscL and MscS -- IV. Pharmacology of Prokaryotic MS Channels -- V. Families of Prokaryotic MS Channels -- A. MscL Family -- B. MscS Family -- VI. Early Origins of Mechanosensory Transduction -- A. Physiological Function of MS Channels in Prokaryotic Cells -- B. Function of MscS-Like Channels in Mechanosensory Transduction in Plants -- VII. Concluding Remarks -- Acknowledgments -- References -- Chapter 3: Activation of Mechanosensitive Ion Channels by Forces Transmitted Through Integrins and the Cytoskeleton -- I. Overview -- II. Introduction. , III. Conventional Views of MS Channel Gating -- IV. Tensegrity-Based Cellular Mechanotransduction -- V. Force Transmission Through Integrins in Living Cells -- VI. Potential Linkages Between Integrins and MS Ion Channels -- VII. Conclusions and Future Implications -- References -- Chapter 4: Thermodynamics of Mechanosensitivity -- I. Overview -- II. Introduction -- A. General Equations -- III. Area Sensitivity -- A. Line Tension and Area Sensitivity -- B. Direct Observations of the Effect of Line Tension and Shape Transformation -- IV. Shape Sensitivity -- A. Experimental Observation of Shape Sensitivity -- V. Length Sensitivity and Switch Between Stretch-Activation and Stretch-Inactivation Modes -- A. Channel Activation by LPLs -- B. Other Parameters Regulating Switch Between Stretch-Activation and Inactivation Modes -- VI. Thermodynamic Approach and Detailed Mechanical Models of MS Channels -- A. Detailed Mechanical Models -- VII. Conclusions -- References -- Chapter 5: Flexoelectricity and Mechanotransduction -- I. Overview -- II. Introduction -- III. Flexoelectricity, Membrane Curvature, and Polarization -- A. Flexoelectricity and Membrane Lipids -- B. Flexoelectricity and Membrane Proteins -- IV. Experimental Results on Flexoelectricity in Biomembranes -- A. Theoretical Remarks -- B. Experimental Data -- V. Flexoelectricity and Mechanotransduction -- VI. Conclusions -- References -- Chapter 6: Lipid Effects on Mechanosensitive Channels -- I. Overview -- II. Intrinsic Membrane Proteins -- III. Effects of Lipid Structure on Membrane Protein Function -- IV. How to Explain Effects of Lipid Structure on Membrane Protein Function -- A. The Lipid Annulus -- B. The Fluidity of a Lipid Bilayer and Its Consequences -- C. The Importance of Hydrophobic Thickness -- D. Curvature Stress -- E. Elastic Strain and Pressure Profiles. , F. General Features of Lipid-Protein Interactions -- V. What Do These General Principles Tell Us About MscL? -- References -- Chapter 7: Functional Interactions of the Extracellular Matrix with Mechanosensitive Channels -- I. Overview -- II. Mechanotransduction -- III. Mechanosensitive Channels in Connective Tissue Cells -- IV. The Extracellular Environment of Cells -- V. Force Transmission from Matrix to Cytoskeleton -- A. Focal Adhesions -- B. Selectins -- VI. Experimental Models of Force Application to Connective Tissue Cells -- VII. Effects of Force on Cell Surface Structures -- VIII. Future Approaches -- References -- Chapter 8: MscL: The Bacterial Mechanosensitive Channel of Large Conductance -- I. Overview -- II. Introduction and Historical Perspective -- A. The Discovery of MS Channels in Bacteria -- B. Proposing a Function -- C. The Identification of Multiple MS Channel Activities in E. coli -- D. Identification of the E. coli mscL Gene -- E. Early Mutagenesis Studies -- III. A Detailed Structural Model: An X-Ray Crystallographic Structure from an E.coli MscL Orthologue -- A. The Crystal Structure -- B. Fitting the Structure with the Findings from Mutagenesis Studies -- C. Comparing Tb-MscL with Eco-MscL -- IV. Proposed Models for How the MscL Channel Opens -- A. Opening the Channel: Twist and Turn -- B. Molecular Dynamic Simulations -- V. Physical Cues for MscL Channel Gating: Protein-Lipid Interactions -- A. Studies of the Energetic and Spatial Parameters for MscL Gating -- B. Does MscL Sense the Pressure Across the Membrane or the Tension Within It? -- C. Sensing the Biophysical Properties of the Membrane -- D. Specific Protein-Lipid Interactions -- VI. MscL as a Possible Nanosensor -- VII. Conclusions -- Acknowledgments -- References -- Chapter 9: The Bacterial Mechanosensitive Channel MscS: Emerging Principles of Gating and Modulation. , I. Overview -- II. Introduction -- III. MscS and Its Relatives -- A. A Brief Account of Bacterial Osmoregulation and the Discovery of MscS -- B. MscS Vs MscK: How to Interpret Early Functional Data? -- C. Purification and Reconstitution of MscS Showed Homo-Multimeric Channels Activated by Tension in the Lipid Bilayer -- IV. Structural and Computational Studies -- A. Structure of MscS and First Hypotheses About Its Gating Mechanism -- B. Computational Studies of MscS -- V. Functional Properties of MscS -- A. MscS Conduction and Selectivity -- B. Gating Characteristics of MscS In Situ -- C. Mutations That Affect MscS Activity -- D. MscS Inactivation -- VI. What Do the Closed, Open, and Inactivated States of MscS Look Like? -- A. Is the Crystal Structure a Native State? -- B. Closed State -- C. Open State -- VII. Emerging Principles of MscS Gating and Regulation and the New Directions -- References -- Chapter 10: StructureFunction Relations of MscS -- I. Overview -- II. Introduction -- A. Functional Overview -- III. The Structure of MscS -- A. The Membrance Domain -- B. The Cytoplasmic Domain -- C. Variations in Structure -- D. Twisting MscS Around the Pore -- E. MscS Is Small but Beautifully Formed -- IV. MscS Mutational Analysis -- V. Structural Transitions in MscS -- A. The Need for the Closed State -- B. The Crystal State -- C. The TM3 Pore -- D. The Closed-to-Open Transition -- VI. Conclusions and Future Perspective -- Acknowledgments -- References -- Chapter 11: The MscS Cytoplasmic Domain and Its Conformational Changes on the Channel Gating -- I. Overview -- II. MscL and MscS: Primary Gates and Similarities in Activation -- III. The MscL Cytoplasmic Regions and Functioning of the Channel -- IV. The MscS C-Terminal Chamber: The Cage-Like Structure and Kinetics -- V. Structural Alterations of the MscS Cytoplasmic Chamber on Gating. , VI. Conclusions and Perspectives -- Acknowledgments -- References -- Chapter 12: Microbial TRP Channels and Their Mechanosensitivity -- I. Overview -- II. A History TRP-Channel Research -- III. The Mechanosensitivity of Animal TRP Channels -- IV. Distribution and the Unknown Origin of TRPs -- V. TRPY1: The TRP Channel of Budding Yeast -- VI. Other Fungal TRP Homologues -- VII. Sequence Information Does Not Explain TRP Mechanosensitivity -- VIII. Conclusions -- Acknowledgment -- References -- Chapter 13: MscS-Like Proteins in Plants -- I. Overview -- II. Mechanosensation and Ion Channels in Plants -- A. Plants Cells and Turgor Pressure -- B. Mechanosensory Signal Transduction in Plants -- C. MS Ion are Present in Plant Cell Membranes -- III. The Eukaryotic Family of MscS_Like Proteins -- A. E. coil MscS -- B. The Eukaryotic Subfamily -- IV. The Arabidopsis MSL Genes -- A.Overview -- B. Subcellular Localization of MSL Proteins -- C. Control of MSL Gene Expression -- D. MSL2, MSL3, and the Control of Organelle Morphology -- V. Outstanding Questions -- A. How Have MscS-Like Proteins Evolved? -- B. What Roles Do MS Ion Channels Play in Plant Biology? -- C. Is Clustering of MS Ion Channels Important? -- V. Conculsion -- References -- Chapter 14: Delivering Force and Amplifying Signals in Plant Mechanosensing -- I. Overview -- II. Introduction -- III. Focusing Force -- A. Force Experienced by a Plant Is Chiefly Borne by the Heterogeneous Wall System -- B. The Plasmalemmal Reticulum Carries Force to the Channels -- C. Implication of Heterogeneous Walls for Thigmotropic Reception -- D. Walls Are Only Half the Mechanical Story: Gravitropism, Like Plant Form, Depends on Force Generated Inside Cells -- E. Not Just Any Displacement Triggers Gravitropism -- F. Map of Mechanotropic Cells in the Root Cap -- IV. Transduction and Ensuing Events in Thigmotropism. , V. Early Events in Gravitropism.
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  • 3
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Cell membranes. ; Free radicals (Chemistry) -- Pathophysiology. ; Cellular signal transduction. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (297 pages)
    Edition: 1st ed.
    ISBN: 9780080920474
    Series Statement: Issn Series
    DDC: 574.875
    Language: English
    Note: Front cover -- Free Radical Effects on Membranes -- Copyright page -- Contents -- Contributors -- Previous Volumes in Series -- Preface -- Part I. Overview -- Chapter 1. Structure and Functions of Biomembranes -- I. Cell Membrane Structure and Function -- II. Overview of Membrane Functions -- III. Calcium Signaling -- IV. Oxidative Stress and Organelle Dysfunction -- References -- Chapter 2. The Interaction of Reactive Oxygen and Nitrogen Species with Membranes -- I. Reactive Oxygen and Nitrogen Species -- II. Physical Interactions: Compartmentalizing Reactivity -- III. Chemical Effects: Lipid Peroxidation -- References -- Part II. Interaction of RONS with Channels and Pumps -- Chapter 3. Modulation of Lung Epithelial Sodium Channel Function by Nitric Oxide -- I. Introduction -- References -- Chapter 4. Effects of Nitrogen Oxides on Chloride Channels -- I. Overview -- II. Introduction -- III. Regulation by Nitrogen Oxides of Swelling-activated Cl- Channels -- IV. Regulation of Calcium Activated Cl- Channels by Nitrogen Oxides (NOx) -- V. Effects of Nitrogen Oxides on CFTR -- VI. Future Directions -- References -- Chapter 5. A Mitochondria-AOS-Kv Channel Axis in Health and Disease -- New Insights and Therapeutic Targets for Vascular Disease and Cancer -- I. Introduction -- II. The Components of the Mitochondria-ROS-Kv Axis -- III. The Mitochondria-AOS-Kv Axis in Hypoxia: HPV -- IV. The Mitochondria-AOS-Kv Axis, Metabolism and Apoptosis -- References -- Chapter 6. Oxidative Modification of Ca2+ Channels, Ryanodine Receptors, and the Sarco/Endoplasmic Reticulum Ca2+-ATPase -- I. Introduction -- II. Overview of Ca2+ Translocation Membrane Proteins -- III. Ca2+ Channels -- IV. SERCA -- V. PMCA -- VI. Concluding Remarks -- References -- Chapter 7. Regulation of Na,K-ATPase by Reactive Oxygen Species -- I. Na,K-ATPase. , II. Na,K-ATPase in Alveolar Fluid Reabsorption -- III. Role of Reactive Oxygen Species in Signaling -- IV. Regulation of Na,K-ATPase and Alveolar Fluid Reabsorption by ROS -- V. Dopamine and beta-adrenergic Agonists Improve ROS-Mediated Decrease in Alveolar Fluid Reabsorption -- VI. Summary -- References -- Part III. RONS and Membrane Permeability -- Chapter 8. Reactive Oxygen Species and Endothelial Permeability -- I. Introduction -- II. Generation and Metabolism of ROS -- III. ROS Generating System in ECs (NADPH Oxidase) -- IV. Regulation of Adherens Junctions (AJs) by Phosphorylation and by Rho GTPase -- V. ROS-generating Stimulants which Regulate Endothelial Permeability -- VI. ROS Reducing Factors/Proteins which Block Endothelial Permeability -- VII. Molecular Targets of ROS Regulating Endothelial Permeability -- VIII. Mediators/Regulators of ROS-dependent Endothelial Permeability -- IX. Functional Significance of ROS-dependent Endothelial Permeability in Vivo -- X. Summary and Conclusions -- References -- Part IV. RONS and Signal Transduction -- Chapter 9. Cell Signaling by Oxidants: Pathways Leading to Activation of Mitogen-activated Protein Kinases (MAPK) and Activator Protein-1 (AP-1) -- I. Introduction -- II. MAPK Signaling -- III. Mitogen-activated Protein Kinase Phosphatases (MKPs) -- IV. Relationships between MAPK and Activator Protein-1 (AP-1) -- V. Conclusions -- References -- Chapter 10. The Interaction of Mitochondrial Membranes with Reactive Oxygen and Nitrogen Species -- I. Mitochondria as a Source of Reactive Species -- II. Effects of ROS and RNS on Mitochondrial Respiration -- III. Mitochondrial Membrane Lipids -- IV. ROS, RNS & -- Mitochondrial Ion Transport -- V. Complex Interactions & -- Concluding Remarks -- References -- Chapter 11. Oxidant Stress and Airway Epithelial Function -- I. Introduction. , II. Sources of Reactive Oxygen Species -- III. Antioxidant Defenses in Airway Epithelium -- IV. Oxidant-induced Airway Epithelial Responses -- V. Conclusions -- References -- Color Plate -- Index.
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  • 4
    Online Resource
    Online Resource
    Burlington :Elsevier Science & Technology,
    Keywords: Cell differentiation. ; Cell membranes. ; Electronic books.
    Description / Table of Contents: CURR TOPICS IN MEMBRANES & TRANSPORT V27.
    Type of Medium: Online Resource
    Pages: 1 online resource (319 pages)
    Edition: 1st ed.
    ISBN: 9780080584980
    Series Statement: Issn Series ; v.Volume 27
    DDC: 571.64
    Language: English
    Note: Front Cover -- Current Topics in Membranes and Transport -- Copyright Page -- Contents -- Preface -- Yale Membrane Transport Processes Volumes -- Part I: Description of Ion Transport Systems in Activated Cells -- Chapter 1. Mitogens and Ion Fluxes -- I . Introduction and Historical Perspective -- II. Ion Transport and pH Regulation in Cells -- III. Changes in Cell Membrane Voltage-Role in the Action of Growth Factors -- IV. Effect of Mitogens on Ion Fluxes and Intracellular pH -- V. Modulation of the Mitogenic Response by Protein Kinase C -- VI. Summary and Perspectives -- VII. Appendix: Measurement of Intracellular pH -- References -- Chapter 2. Na+-H+ and Na+-Ca2+ Exchange in Activated Cells -- I. Introduction -- II. Na+-Ca2+ Exchange -- III. Na+-H+ Exchange -- IV. Pharmacological Definition of the Na+-H+ and Na+-Ca2+ Exchange Systems -- V. Summary -- References -- Chapter 3. Chloride-Dependent Cation Cotransport and Cellular Differentiation: A Comparative Approach -- I. Introduction -- II. General Properties -- III. Properties in Blood Cells at Various Stages of Differentiation -- IV. Properties in Differentiated Epithelial Cells -- V. Nonepithelial Cells as Models for Cotransport during Differentiation -- VI . Conclusion -- Note Added in Proof -- References -- Part II: Triggers for Increased Transport during Activation -- Chapter 4. External Triggers of Ion Transport Systems: Fertilization, Growth, and Hormone Systems -- I. Introduction -- II. Ionic Responses to Fertilization -- III. Serum and Growth Factor Activation of Ionic Transport Systems in Cultured Cells and Lymphocytes -- IV. Hormonal Stimulation of Ion Transport and Hormone Secretion -- V. Concluding Remarks -- References -- Chapter 5. Early Stimulation of Na+-H+ Antiport, Na+-K+ Pump Activity, and Ca2+ Fluxes in Fibroblast Mitogenesis -- I. Introduction. , II. Ionic Responses Elicited by Growth Factors in Quiescent Cells -- III. Protein Kinases and Ion Fluxes -- IV. Calcium Fluxes -- V. Conclusions and Perspectives -- References -- Chapter 6. Volume-Sensitive Ion Fluxes in Amphiuma Red Blood Cells: General Principles Governing Na-H and K-H Exchange Transport and Cl-HCO3 Exchange Coupling -- I. Introduction: The Role of Alkali Metal-H Exchange in Cell Regulatory Processes -- II. Thermodynamic Principles of lon Transport: Electroneutral versus Conductive Alkali Metal Ion Fluxes -- III. Volume-Sensitive Ion Fluxes in Amphiuma Red Blood Cells -- IV. Ca2+-Dependent Alkali Metal Ion Flux in Amphiuma Red Blood Cells -- V. The Nature of Net Na Flux by Amphiuma Red Blood Cells in Hyperosmotic Media -- VI. Cl-HCO3 Exchange and Its Functional Relationship to Alkali Metal-H Exchange, Alkali Metal-Cl Cotransport, and Parallel Alkali Metal and H or Cl Conductance Pathways -- VII. Activation and Control of Alkali Metal-H Exchange in Amphiuma Red Blood Cells -- VIII. Summary -- References -- Part III: Consequences of the Alterations in Ion Transport Observed during Activation -- Chapter 7. Intracellular Ionic Changes and Cell Activation: Regulation of DNA, RNA, and Protein Synthesis -- I. Introduction -- II. DNA Synthesis -- III. RNA Synthesis -- IV. Protein Synthesis -- V. Posttranslational Events Influencing Intracellular Traffic and Cell Surface Expression of Proteins -- VI. Conclusions -- References -- Chapter 8. Energy Metabolism of Cellular Activation, Growth, and Transformation -- I. Introduction -- II. Control of Energy Metabolism in Adult Cells That Maintain a Relatively Constant Metabolic Rate -- III. Control of Energy Metabolism of Adult Cells That Can Be Rapidly Activated -- IV. Energy Metabolism of Cells in Culture -- V. Energy Metabolism of Malignant Cells -- References -- Index.
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  • 5
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Biological transport. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (477 pages)
    Edition: 1st ed.
    ISBN: 9780080585109
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- Developmental Biology of Membrane Transport Systems -- Copyright Page -- Contents -- Contributors -- Foreword -- Preface -- Previous Volumes in Series -- Part I: Molecular Biology of Transport Proteins and Membrane Protein Sorting -- Chapter 1. Molecular Biology of Membrane Transport Proteins -- I. Introduction -- II. The Coding of Membrane Protein Structure -- III. Model Structures -- IV. Conclusions and Perspectives -- References -- Chapter 2. Biogenesis and Sorting of Plasma Membrane Proteins -- I. Introduction -- II. Biogenesis of Membrane Proteins -- III. Sorting and Epithelial Polarity -- IV. Conclusion -- References -- Part II: Fertilization and Early Embryonic Development -- Chapter 3. Electrical Characteristics of Oocytes and Eggs -- I. Introduction -- II. Ion Channels in Oocytes and Mature Eggs -- III. Electrical Characteristics of Oocytes -- IV. Fertilization -- V. Conclusions -- References -- Chapter 4. Ion and Solute Transport in Preimplantation Mammalian Embryos -- I. Introduction -- II. Ion Transport -- III. Fluid Transport -- IV. Sugar Transport -- V. Protein Transport -- VI. Amino Acid Transport -- VII. Summary and Prospects -- References -- Part III: Developmental Biology of Ion and Solute Co- and Counter-Transport -- Chapter 5. Cell Biology and Molecular Genetics of Enterocyte Differentiation -- I. Introduction -- II. Markers of Enterocyte Differentiation -- III. Fetal Development -- IV. Enterocyte Differentiation in Adult Intestine -- V. Enterocyte Differentiation in Vitro -- VI. Disease Effects on Enterocyte Differentiation -- VII. Barrier Function and Enterocyte Development -- VIII. Concluding Remarks -- References -- Chapter 6. Ion Transport and Adenylyl Cyclase System in Red Blood Cells -- I. Introduction -- II. Hormone-Sensitive Adenylyl Cyclase System -- III. Effects of cAMP on Ion Channels and Transport. , IV. Adenosine Influence on Ion Movements -- V. Conclusions -- References -- Part IV: Ion Channel Development -- Chapter 7. Development, Maintenance, and Modulation of Voltage-Dependent Sodium Channel Topography in Nerve Cells -- I. Introduction -- II. Molecular Properties of Voltage-Dependent Sodium Channels -- III. Localization and Maintenance of Voltage-Dependent Sodium Channels -- IV. Differentiation of the Axon Membrane: Localization of Sodium Channels in Developing Nerve -- V. Conclusions and Perspectives -- References -- Chapter 8. Biogenesis of the Mouse Muscle Nicotinic Acetylcholine Receptor -- I. Introduction -- II. Subunit Structure and Processing -- III. Assembly -- IV. Conclusions -- References -- Note Added in Proof -- Chapter 9. Functional Properties of Voltage-Dependent Calcium Channels -- I. Introduction -- II. Ca2+ Selectivity -- III. Voltage-Dependent Activation -- IV. Inactivation -- V. Facilitation and Gating Modes -- VI. Different Types of Ca2+ Channels -- VII. Summary -- References -- Chapter 10. Potassium Channels in Developing Excitable Cells -- I. Introduction -- II. K+ Channels in Developing Neurons -- III. Smooth Muscle Cells and K(Ca) Channels -- IV. K+ Channels in Developing Drosophila -- V. Cell Interaction and Ion Channel Development -- VI. Recapitulation and Coda -- References -- Chapter 11. Potassium Channels in Development, Activation, and Disease in T Lymphocytes -- I. Introduction -- II. Properties of K+ Channels in Lymphocytes -- III. Molecular Basis of K+ Channel Diversity -- IV. Voltage-Gated K+ Channels in Development -- V. K+ Channels and T Cell Function -- VI. Voltage-Gated K+ Channels in Autoimmune Diseases -- VII. Conclusions -- References -- Chapter 12. Development of Epithelial Na+ Channels and Regulation by Guanine Nucleotide Regulatory (G) Proteins and Phospholipids -- I. Introduction. , II. Developmental Expression of Epithelial Na+ Channels -- III. Regulation of Na+ Channel Activity -- IV. Conclusions and Perspective -- References -- Index.
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  • 6
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Sodium channels. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (425 pages)
    Edition: 1st ed.
    ISBN: 9780080585185
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- Amiloride-Sensitive Sodium Channels Physiology and Functional Diversity -- Copyright Page -- Contents -- Contributors -- Preface -- Previous Volumes in Series -- PART I: Structure-Function Relations of Amiloride-Sensitive Sodium Channels -- Chapter 1. Mapping Structure/Function Relations in αbENaC -- I. Introduction -- II. Cloning and Expression of αbENaC -- III. The C Terminus of αbENaC: A Kinetic Switch? -- IV. A Region in the Extracelular Loop Influences Gating, Ion Selectivity, and Amiloride Affinity -- V. Summary -- References -- Chapter 2. Membrane Topology, Subunit Composition, and Stoichiometry of the Epithelial Na+ Channel -- I. Introduction -- II. Topology of ENaC -- III. Subunit Composition of hENaC -- IV. Stoichiometry of hENaC -- V. Conclusion -- References -- Chapter 3. Subunit Stoichiometry of Heterooligomeric and Homooligomeric Epithelial Sodium Channels -- I. Introduction -- II. Stoichiometry of Heterooligomeric αβγ Na+ Channels -- III. α-Subunit Stoichiometry -- IV. β-Subunit and γ- Subunit Stoichiometry -- V. Stoichiometry of Homooligomeric α-Subunit Na+ Channels -- References -- PART II: Regulation of Sodium Channels -- Chapter 4. Cell-Specific Expression of ENaC and Its Regulation by Aldosterone and Vasopressin in Kidney and Colon -- I. Introduction -- II. Cell-Specific Expression -- III. Regulation of ENaC Expression by Aldosterone and Vasopressin -- References -- Chapter 5. Regulation of ENaC by Interacting Proteins and by Ubiquitination -- I. Introduction -- II. Proline-Rich Regions in ENaC and Their Interacting Proteins -- III. Nedd4: Its Domains and Mode of Interaction with ENaC -- IV. Regulation of ENaC Stability and Function by Ubiquitination -- V. Role of the C2 Domain of Nedd4 in Ca2+-Dependent Membrane Targeting -- VI. Summary -- References. , Chapter 6. Role of G Proteins in the Regulation of Apical Membrane Sodium Permeability by Aldosterone in Epithelia -- I. Introduction -- II. Control of Basal Na+ Transport by G Proteins -- III. GTP-Dependent Methylation of Membrane Proteins -- IV. Control of Basal Na+ Permeability by Methylation -- V. Aldosterone-Dependent Methylation of Membrane Proteins -- VI. Aldosterone-Dependent Membrane GTPase Activity -- VII. The Effect of Pertussis Toxin on Membrane Na+ Transport and GTPase Activity -- VIII. The Effect of Aldosterone on G-Protein Expression -- IX. Conclusion -- References -- Chapter 7. The Role of Posttranslational Modifications of Proteins in the Cellular Mechanism of Action of Aldosterone -- References -- Chapter 8. Regulation of Amiloride-Sensitive Na+ Channels in the Renal Collecting Duct -- I. Introduction -- II. Vasopressin Can Act as an Antinatriuretic as Well as an Antidiuretic Hormone -- III. Autacoids That Limit the Actions of Aldosterone and Vasopression in the CCD -- IV. Trafficking and the Regulation of the Amiloride-Sensitive Na+ Channel -- V. A Challenge for Integrative Physiology-The Link between Na+ Retention and Hypertension -- References -- Chapter 9. CAMP-Mediated Regulation of Amiloride-Sensitive Sodium Channels: Channel Activation or Channel Recruitment? -- I. Introduction -- II. Evidence for cAMP-Mediated Activation of Amiloride-Sensitive Sodium Channels -- III. Evidence for cAMP-Mediated Recruitment of Amiloride-Sensitive Sodium Channels -- IV. Perspectives -- References -- Chapter 10. Human Lymphocyte Ionic Conductance -- I. Introduction -- II. Lymphocyte Potassium Channels and Cell Cycle Regulation -- III. Cell-Cycle-Dependent Expression of Chloride Channels by Human Lymphocytes -- IV. CD20: A B-Lymphocyte-Specific Unique Calcium Conductor -- V. Lymphocyte Amiloride-Sensitive Sodium Conductance -- References. , Chapter 11. Regulatory Aspects of Apx, a Novel Na+ Channel with Connections to the Cytoskeleton -- I. Sodium Channels of A6 Epithelial Cells -- II. Apx, an Actin-Regulated Sodium Channel -- III. Sodium Transport in Proximal Tubular Cells -- IV. Conclusion and Perspective -- References -- PART III: Sodium Channels in the Lung -- Chapter 12. Species-Specific Variations in ENaC Expression and Localization in Mammalian Respiratory Epithelium -- I. Introduction -- II. Structure/Function of the Respiratory Tract -- III. Regional ENaC Expression in the Respiratory Tract -- IV. Developmental Expression of ENaC in the Lung -- V. Expression Patterns and ENaC Function -- References -- Chapter 13. Inhibition of Vectorial Na+ Transport across Alveolar Epithelial Cells by Nitrogen-Oxygen Reactive Species -- I. Introduction -- II. Interaction of *NO with Biological Targets: Signal Transducer and Pathophysiological Mediator -- III. Modulation of Ion Transport across the Adult Alveolar Epithelium by Redox States of *NO -- IV. Inhibition of Na+ Transport across Freshly Isolated ATII Cells by Redox States of *NO -- V. Does *NO Modulate Alveolar Epithelial Fluid Transport in Vivo? -- VI. Conclusions -- References -- Chapter 14. Induction of Epithelial Sodium Channel (ENaC) Expression and Sodium Transport in Distal Lung Epithelia by Oxygen -- I. Introduction -- II. Physiologic Increase in Oxygen Augments Na+ Transport in FDLE -- III. Oxygen Induction of Na+ Transport Is Mediated by Reactive Oxygen Species -- IV. Increase in ENaC mRNA Expression Is Associated with NF-KB Activation -- V. Possible Sites of ROS Generation for Oxygen Induction of Na+ Transport in FDLE -- VI. Conclusion -- References -- Chapter 15. Catecholamine Regulation of Amiloride-Sensitive Na+ Transport in the Fetal Rat Alveolar Epithelium -- I. Introduction. , II. Characteristics of Amiloride-Sensitive Na+-Permeable Channels -- III. Catecholamine Action -- IV. Switching Mechanism of FDLE to the Absorptive from the Secretory Tissue by Catecholamine -- V. Conclusion -- References -- Chapter 16. Cyclic Nucleotide-Gated Cation Channels Contribute to Sodium Absorption in Lung: Role of Nonselective Cation Channels -- I. Nonselective Cation Channels in Epithelia -- II. Analogues of Amiloride Block Multiple Types of Cation Channels -- III. The Role of ENaC and Other Channels in Transepithelial Transport in Lung -- IV. Nucleotide-Gated Nonselective Cation Channels (αCNC1, αCNC2, αCNC3, βPCNCab) -- V. Cyclic Nucleotide-Gated Channels in the Lung -- References -- PART IV: Sensory and Mechanical Transduction -- Chapter 17. C. elegans Members of the DEG/ENaC Channel Superfamily: Form and Function -- I. Introduction -- II. C. elegans Proteins Related to ENaC Channels Define Two Subfamilies -- III. C. elegans Degenerins Have Been Implicated in Mechanotransduction -- IV. Future Directions -- References -- Chapter 18. Amiloride-Sensitive Sodium Channels in Taste -- I. Introduction and Historical Background -- II. The Frog Sodium Taste Channel -- III. Amiloride-Sensitive Na+ Channels in Rodent Tongue -- IV. ENaC Expression in the Lingual Epithelium (LE) -- V. ENaC Expression in Taste Buds -- VI. Development and Plasticity of the Channel -- VII. Outlook -- References -- PART V: Clinical Relevance -- Chapter 19. The involvement of Amiloride-Sensitive Na+ Channels in Human Genetic Hypertension: Liddle's Syndrome -- I. Introduction -- II. Molecular Mechanism of ENaC-Gated Function: Increased Surface Density or Increased Single-Channel Open Probability, or Both -- III. Summary -- References -- Chapter 20. Epithelial Sodium Channels in Cystic Fibrosis -- I. Introduction -- II. Na+ Hyperabsorption in CF -- III. ENaCs and CFTR. , IV. CFTR-Induced Inhibition of ENaCs and Cell Regulatory Machinery -- V. Alpha, Beta, or Gamma? -- VI. Mutations of CFTR Found in CF and Inhibition of αβγ-ENac -- VII. Concluding Remarks -- References -- Index.
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  • 7
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Biological transport. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (443 pages)
    Edition: 1st ed.
    ISBN: 9780080585192
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- Membrane Permeability: 100 Years since Ernest Overton -- Copyright Page -- Contents -- Contributors -- Tribute -- Previous Volumes in Series -- Chapter 1. Charles Ernest Overton's Concept of a Cell Membrane -- I. A Brief Biography of Ernest Overton -- II. The Exchange of Solutes across the Cell Boundary -- III. Meyer-Overton Theory of Narcosis -- IV. Role of Cations in the Excitability Process -- V. Overton's Scientific Personality -- References -- Chapter 2. Structure and Physical Properties of the Lipid Membrane -- I. Bilayers in Biological Membranes -- II. Phase Behavior of Membrane Phospholipids -- III. Structure of Phospholipid Bilayers -- IV. Stability and Mechanical Properties of Bilayers -- V. Interbilayer Interactions -- VI. Roles of Specific Lipids in Membrane Bilayers -- VII. Summary -- References -- Chapter 3. Insights from Computer Simulations into the Interactions of Small Molecules with Lipid Bilayers -- I. Introduction -- II. Methods of Simulation -- III. Distribution of Solutes in a Bilayer -- IV. Membrane Permeability of Small Molecules -- V. Summary -- References -- Chapter 4. Membrane Permeability Barriers to Ionic and Polar Solutes -- I. Introduction -- II. Overton's Concept of Membrane Permeability -- III. Permeation by the Solubility-Diffusion Mechanism -- IV. Permeation through Transient Pores -- V. Proton Permeation -- VI. Summary -- References -- Chapter 5. Water Permeation across Membranes -- I. Introduction -- II. Biophysics of Water Transport -- III. Water Transport across Lipid Membranes -- IV. Water Transport across Biological Membranes: Water Channels -- V. Summary -- References -- Chapter 6. Membrane Events Involved in Volume Regulation -- I. Introduction: Biological Role -- II. Membrane Transport Mechanisms in Regulatory Volume Decrease (RVD). , III. Membrane Transport Systems Involved in Volume Regulatory Increase (RVI) -- IV. Volume Sensing and Signal Transduction -- V. Cytoskeleton and Cell Volume Regulation -- VI. Summary -- References -- Chapter 7. Interaction of Natural and Model Peptides with Membranes -- I. Introduction -- II. Free Energy of Peptide Binding to Membranes -- III. Factors Influencing Peptide Structure and Orientation in Membranes -- IV. Summary -- References -- Chapter 8. Lateral Diffusion of Lipids and Proteins -- I. Introduction -- II. The Key Question -- III. Theoretical Developments -- IV. Factors Controlling Lateral Diffusion -- V. Applications to Membranes -- VI. Summary -- References -- Chapter 9. A Short History of Ion Channels and Signal Propagation -- I. Introduction -- II. Ionic Currents in Axons -- III. Carriers, Pores, Gates, and Selectivity before Cloning -- IV. The Age of Cloning -- V. Summary -- References -- Chapter 10. Lipid Membrane and Ligand-Gated Ion Channels in General Anesthetic Action -- I. Introduction -- II. The Meyer-Overton Hypothesis and the Evolution of Lipid-Based Theories of Anesthesia -- III. The Rise of Protein-Based Theories of Anesthetic Action -- IV. Future Directions -- V. Summary -- References -- Chapter 11. Plasma Membrane-Localized Signal Transduction -- I. Introduction -- II. Membrane Receptor-Mediated Signaling: Biochemical Mechanisms -- III. Signal Amplification -- IV. The Plasma Membrane as an Integration Site for Signal Transduction -- V. Summary -- References -- Chapter 12. Active Transport and Pumps -- I. Introduction -- II. Pumps -- III. Summary -- References -- Index.
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  • 8
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Biological transport. ; Membranes (Biology). ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (191 pages)
    Edition: 1st ed.
    ISBN: 9780080585123
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- Cell Biology and Membrane Transport Processes -- Copyright Page -- Contents -- Contributors -- Preface -- Previous Volumes of Membranes and Transport -- Part I: The Multidrug Resistance Family of Transporters -- Chapter 1. The Multidrug Transporter: Mechanistic Considerations -- I. Introduction: The Problem of Multidrug Resistance in Cancer -- II. General Structural Features of the Multidrug Transporter -- III. Evidence Indicating That P-Glycoprotein Is Not a Classical Transmembrane Transporter Suggests a New Model for Drug Efflux -- IV. Identification of Photolabeled Sites in P-Glycoprotein -- V. Substrate Recognition Regions and Labeling Sites Are Different -- VI. ATP Is the Preferred Energy Source for in Vitro Transport -- VII. Conclusions -- References -- Chapter 2. A Novel Mechanism for Transmembrane Translocation of Peptides: The Saccharomyces cerevisiae STE6 Transporter and Export of the Mating Pheromone a-Factor -- I. Introduction -- II. Yeast a-Factor Export Requires an ABC-Type Transporter -- III. STE6 Transporter Is an Integral but Unglycosylated Plasma Membrane-Associated Protein -- IV. Level and Localization of STE6 Transporter Are Regulated -- V. Mammalian Mdr Transporters Expressed in Yeast Can Mediate a-Factor Export -- VI. Multiple Dedicated Transporters for Peptide Export and Intercompartmental Protein Trafficking in Eukaryotic Cells -- VII. Conclusions and Prospectus -- References -- Part II: Structure-Function Relationships in Ion Pumps -- Chapter 3. Structural Requirements for Subunit Assembly of the Na,K-ATPase -- I. Regulation of the Na,K-ATPase -- II. Subunit Assembly as a Critical Step for Regulatory Control of the Na,K-ATPase -- III. Assembly Assay by Coprecipitation with Subunit-Specific Monoclonal Antibodies -- IV. Kinetics of Subunit Assembly: Why They May Be Complex. , V. Transfection Experiments for Studies of Subunit Assembly -- VI. Topology Models and Insights into Assembly Requirements -- VII. β-Subunit Features Required for Assembly with α-Subunits -- VIII. Chimeras for Studies of Assembly Requirements of the α-Subunit -- IX. The Isoforms Issue in Assembly -- X. Conclusions -- References -- Chapter 4. Structure-Function Relationship of Na,K-ATPase: The Digitalis Receptor -- I. Introduction -- II. General Properties of Cardiac Glycosides -- III. Physiological Role and Heterogeneity of the Digitalis Receptor -- IV. Structure-Function Relationship of the Digitalis Receptor -- V. Conclusions and Perspectives -- References -- Part III: Sorting of Ion Transport Proteins and the Creation of Polarized Membrane Domains -- Chapter 5. Subcellular Targeting and Regulation of Glucose Transporters -- I. Introduction -- II. Intracellular Targeting of GLUT4 Is Isoform-Specific and Independent of Cell Type -- III. The Structural Requirements for GLUT4 Targeting Are under Investigation -- IV. The Mechanism of GLUT4 Targeting Is Unknown -- V. Conclusions -- References -- Chapter 6. Plasticity in Epithelial Polarity -- I. Introduction -- II. Two Types of Intercalated Cell with Reversed Polarity -- III. Plasticity in Epithelial Polarity -- IV. The Apical and Basolateral Cl/HCO3 Exchangers Are Both AE1 -- V. Plasticity of Epithelial Polarity in Vitro -- VI. Potential Mechanisms by Which ECM Proteins Determine Polarity in Intercalated Cells -- References -- Chapter 7. Regulation of Cell Adhesion and Development of Epithelial Cell Surface Polarity -- I. Perspective -- II. Regulation of Cell Adhesion -- III. The Cadherin Family of Cell Adhesion Proteins -- IV. Interactions between Cadherins and Cytoplasmic (Cytoskeletal) Proteins -- V. Role of Cadherins in Cell Surface Remodeling of Membrane Proteins. , VI. Regulation of Na,K-ATPase Distribution during Formation of Polarized Epithelial Cells -- VII. Regulation of Membrane-Cytoskeleton Assembly -- VIII. Regulation of Development of Cell Surface Polarity of Other Membrane Proteins -- IX. Mechanisms of Induction of Cell Morphogenesis by Cadherins -- References -- Chapter 8. Synthesis and Sorting of Ion Pumps in Polarized Cells -- I. Introduction -- II. Sorting Signals: Ion Pumps in Polarized Epithelial Cells -- III. Epithelial and Neuronal Sorting: Similarities and Differences -- IV. Sorting Machinery: A Genetic Approach -- V. Conclusions -- References -- Index.
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  • 9
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Aqueous humor. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (520 pages)
    Edition: 2nd ed.
    ISBN: 9780080920511
    Series Statement: Issn Series
    DDC: 612.844
    Language: English
    Note: Front Cover -- The Eye's Aqueous Humor -- Copyright Page -- Contents -- Contributors -- Preface -- Previous Volumes in Series -- Chapter 1: Formation of the Aqueous Humor: Transport Components and Their Integration -- I. Overview -- II. Introduction -- III. Structure of Ciliary Epithelium -- IV. Unidirectional Secretion of Aqueous Humor -- V. Potential Unidirectional Reabsorption of Aqueous Humor -- VI. Regulation of Net Aqueous Humor Secretion -- VII. Summary of Current Views, Recent Advances, and Future Directions -- References -- Chapter 2: Ocular Aquaporins and Aqueous Humor Dynamics -- I. Overview -- II. Introduction -- III. Aquaporins are assembled as four homomeric subunits -- IV. Ocular Distribution of Aquaporins -- V. Aquaporins and Aqueous Humor Dynamics -- VI. Ion Channel Activity of AQP1 -- VII. Aquaporin and Ion Channel Interactions -- VIII. Future Directions -- References -- Chapter 3: The Role of Gap Junction Channels in the Ciliary Body Secretory Epithelium -- I. Overview -- II. Introduction -- III. General Properties of Connexins Including Those Composing the Ciliary Body Epithelium Gap Junctions -- IV.Modeling of Fluid Transport by the Ciliary Epithelium -- V.Animal Models Support a Role for Gap Junctions in Fluid Transport by Ocular Epithelia -- References -- Chapter 4: Regional Dependence of Inflow: Lessons from Electron Probe X-ray Microanalysis -- I. Overview -- II. Introduction -- III. Review of Electron-probe X-ray Microanalysis -- IV. Total Inflow -- V. Topography of Inflow -- VI. A New Model for Aqueous Humor Production -- VII. Effect of Timolol on Inflow -- VIII. Future Directions -- References -- Chapter 5: Functional Modulators Linking Inflow with Outflow of Aqueous Humor -- I. Overview -- II. Introduction -- III. Sources of Neuropeptides and Peptide Hormones in the AqH. , IV.Neuroendocrine Characteristics of the Bilayered CE -- V.Neuroendocrine Phenotype of the TM -- VI. Regulation of Neuroendocrine Signals: The Potential Role of Neutral Endopeptidase 24.11 (Neprelysin) -- VII. Neuroendocrine Signaling in the CE and TM -- VIII. Putative Glutamatergic System in the Inflow-Outflow Axis: Glutamate as a Functional Endocrine/Paracrine Signal Between -- IX. Implications of a Neuroendocrine Signaling in the Anterior Segment of the Eye -- X. Summary -- Acknowledgments -- References -- Chapter 6: Aqueous Humor Outflow Resistance -- I. Overview -- II. Introduction -- III. The Aqueous Humor -- IV. Regions of Low Outflow Resistance -- V. Regions of Potential Significant Outflow Resistance -- VI. Endothelial Lining of Schlemm's Canal -- VII. Summary -- References -- Chapter 7: Aqueous Humor Dynamics I -- I. Overview -- II. Components of Aqueous Humor Dynamics and Measurement Techniques -- III. Aqueous Humor Dynamics in Research Animals -- IV. Summary -- Acknowledgment -- References -- Chapter 8: Aqueous Humor Dynamics II -- I. Overview -- II. Introduction -- III. Normal Values of Aqueous Humor Dynamics in Humans -- IV. Clinical Syndromes -- V. Drugs Affecting Aqueous Humor Dynamics -- VI. Summary -- References -- Chapter 9: Effects of Circulatory Events on Aqueous Humor Inflow and Intraocular Pressure -- I. Overview -- II. IOP Effects on Ocular Blood Flow -- III. Ocular Blood Flow Effects on IOP -- IV. Ciliary Blood Flow and Aqueous Production -- V. Episcleral Venous Pressure and IOP -- VI. Conclusion -- Acknowledgments -- References -- Chapter 10: Retinal Ganglion Cells and Glaucoma: Traditional Patterns and New Possibilities -- I. Overview -- II. Introduction -- III. Influences on Glaucomatous Damage to Ganglion Cells -- IV. Mechanisms of Ganglion Cell Death -- V. Conclusion -- Acknowledgements -- References. , Chapter 11: What is Functional Genomics Teaching us about Intraocular Pressure Regulation and Glaucoma? -- I. Overview -- II. Introduction -- III. Functional Genomics: Microarrays, Proteomics and Protein Modification -- IV. Tissues Involved in the Development of Glaucoma. Survey of Microarray Studies -- V. The Trabecular Meshwork Tissue: Expressed Genes (CDNA) and Proteins Obtained by Direct Sequencing and Mass Spectrometry -- VI. The Trabecular Meshwork Tissue: In Search of Genes Responding to Glaucomatous Insults -- VII. Proposed Molecular Signature of Human Glaucoma -- Acknowledgments -- References -- Chapter 12: Molecular Approaches to Glaucoma: Intriguing Clues for Pathology -- I. Overview -- II. Transforming Growth Factor-B -- III. Thrombospondin-1 -- IV. Connective Tissue Growth Factor -- V. Bone Morphogenetic Protein-7 -- VI. Myocilin -- VII. Optineurin -- VIII. WD Repeat Domain 36 -- IX. Conclusion -- References -- Chapter 13: Outflow Signaling Mechanisms and New Therapeutic Strategies for the Control of Intraocular Pressure -- I. Overview -- II. Introduction -- III. New Approaches for IOP Lowering -- IV. Future Therapeutic Opportunities -- References -- Index -- Color Plate.
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  • 10
    Online Resource
    Online Resource
    San Diego :Elsevier Science & Technology,
    Keywords: Physiology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (311 pages)
    Edition: 1st ed.
    ISBN: 9780080585161
    Series Statement: Issn Series
    Language: English
    Note: Front Cover -- The Eye's Aqueous Humor From Secretion to Glaucoma -- Copyright Page -- Contents -- Contributors -- Preface -- Previous Volumes in Series -- Chapter 1. Transport Components of Net Secretion of the Aqueous Humor and Their Integrated Regulation -- I. Introduction -- II. Structure of Ciliary Epithelium -- III. Overview of Net Secretion by Ciliary Epithelium -- IV. Unidirectional Secretion -- V. Unidirectional Absorption -- VI. Coordinated Effects on Secretion and Absorption -- References -- Chapter 2. Molecular Approaches to the Study of the Na+,K+-ATPase and Chloride Channels in the Ocular Ciliary Epithelium -- I. Introduction -- II. Na+,K+-ATPase -- III. Regulation of Na+,K+-ATPase -- IV. Molecular Characterization of the Chloride Channel CIC-3 and the Chloride Channel Regulator, PICln in the Ocular Ciliary Epithelium -- V. Additional Transporter Genes Identified in the Ocular Ciliary Epithelium -- References -- Chapter 3. Chloride Channels in the Ciliary Epithelium -- I. Introduction -- II. Volume-Activated Chloride Channels -- III. Agonist- Activated Chloride Channels -- IV. Anion-Selective Channels -- V. Nonselective Channels -- VI. Role of Chloride Channels -- References -- Chapter 4. Identification of Potassium Channels in Human Lens Epithelium -- I. Introduction -- II. Electrophysiological Characterization -- III. Molecular Biological Characterization -- IV. Summary -- References -- Chapter 5. Aquaporin Water Channels in Eye and Other Tissues -- I. Introduction -- II. Discovery of the Aquaporins -- III. Molecular Structure -- IV. Genetic Origins of the Aquaporins -- V. Distribution and Physiology -- VI. Summary -- References -- Chapter 6. Gap Junctions and Interlayer Communication in the Heterocellular Epithelium of the Ciliary Body -- I. Introduction -- II. The Gap Junction -- III. Gap Junctions of the Ciliary Body. , IV. Functional Studies of Junctional Communication -- V. Summary -- References -- Chapter 7. The Trabecular Meshwork and Aqueous Humor Reabsorption -- I. Introduction -- II. Electrophysiology of Cultured Trabecular Meshwork Cells -- III. Intracellular Calcium -- IV. Regulation of Intracellular pH -- V. Direct Measurement of Contractility of Isolated Trabccular Meshwork and Ciliary Muscle Strips -- VI. Measurement of Contraction of Cultured Trabecular Meshwork Cells -- VII. The Perfused Anterior Segment -- VIII. Summary of Channels, Transporters, and Receptors in the Trabecular Meshwork Cell -- IX. Functional Synergism/Antagonism Between Trabecular Meshwork and Ciliary Muscle -- X. Summary -- References -- Chapter 8. Circadian Rhythms in Aqueous Humor Formation -- I. Historical Summary of Investigations -- II. Methods -- III. Homologous Desensitization of Circadian Aqueous Flow -- IV. Do Gap Junctions Participate in the Circadian Rhythm of Aqueous Flow? -- V. Summary -- References -- Chapter 9. Clinical Measurements of Aqueous Dynamics: Implications for Addressing Glaucoma -- I. Clinical Components of Aqueous Dynamics -- II. Fluorescein Washout Method of Measuring Aqueous Flow -- III. Observations Based on Clinical Measurements in Volunteers -- IV. Observations in Clinical Syndromes -- V. Effects of Pharmaceutical Agents -- VI. Noninvasive Measurement of Other Parameters of Aqueous Humor -- VII. Summary and Future Challenges -- References -- Index.
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