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
URL:
https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=404352
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.
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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.
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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.
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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.
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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.
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Chapter 22. Molecular Basis of Deafness Due to Mutations in the Connexin26 Gene (GJB2).
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