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  • 1
    Online-Ressource
    Online-Ressource
    San Diego :Elsevier Science & Technology,
    Schlagwort(e): Peptides. ; Electronic books.
    Materialart: Online-Ressource
    Seiten: 1 online resource (392 pages)
    Ausgabe: 1st ed.
    ISBN: 9780081008522
    DDC: 610.28/4
    Sprache: Englisch
    Anmerkung: Front Cover -- Peptides and Proteins as Biomaterials for Tissue Regeneration and Repair -- Copyright -- Contents -- Contributors -- Preface -- Peptides and proteins as biomaterials for tissue regeneration and repair -- Chapter 1: Fundamentals of protein and cell interactions in biomaterials -- 1.1 Fundamentals of protein adsorption on biomaterials -- 1.1.1 Basics of protein adsorption -- 1.1.1.1 Function and structural organization -- 1.1.1.2 Structure and orientation of adsorbed proteins -- 1.1.2 Interactions with the surface: hydrophobic and electrostatic bonding -- 1.1.3 Kinetics of protein adsorption -- 1.1.4 Conformational changes and stability -- 1.1.5 Reversibility of protein adsorption -- 1.1.6 Competitive adsorption behavior -- 1.2 Biomaterial surface properties and their effect on protein adsorption -- 1.2.1 Promoting protein adsorption: Osseointegration -- 1.2.2 Preventing protein adsorption: Hemocompatibility -- 1.3 Quantification of protein adsorption -- 1.3.1 Optical -- 1.3.1.1 Ellipsometry -- 1.3.1.2 Surface plasmon resonance -- 1.3.2 Spectroscopic -- 1.3.2.1 Fluorescent spectroscopy -- 1.3.2.2 Infrared absorption spectroscopy -- 1.3.3 Microscopic -- 1.3.3.1 Atomic force microscopy (AFM) -- 1.3.4 Radiolabeling -- 1.3.5 Quartz crystal microbalance with dissipation monitoring (QCM-D) -- 1.4 The importance of adsorbed proteins in the tissue reaction to biomaterials -- 1.4.1 Effect of adsorbed proteins on cell adhesion -- 1.4.2 Effect of adsorbed proteins on cell activation -- 1.4.3 Effect of adsorbed proteins on the FBR -- 1.5 Quantification/detection of cell adhesion and activation -- 1.5.1 Cell adhesion -- 1.5.1.1 Micropatterning -- 1.5.1.2 Three-dimensional traction force microscopy (3D-TFM) -- 1.5.1.3 QCM-D -- 1.5.1.4 Microfluidic -- 1.5.1.5 AFM -- 1.5.2 Cell activation -- 1.5.2.1 Fluorescence microscopy -- 1.5.2.2 Flow cytometry. , 1.5.2.3 Enzyme-linked immunosorbent assay (ELISA) -- 1.6 Concluding remarks -- References -- Chapter 2: Extracellular matrix constitution and function for tissue regeneration and repair -- 2.1 An overview of ECM structure and function -- 2.1.1 Architectural role -- 2.1.2 Adhesion mediator -- 2.1.3 Mechanosensor -- 2.1.4 Growth factor reservoir and modulator of signaling peptides -- 2.2 Major ECM components -- 2.2.1 Collagen -- 2.2.2 Proteoglycans -- 2.2.3 Other ECM molecules -- 2.2.4 Matrix-degrading enzymes -- 2.3 ECM dynamics in development -- 2.3.1 General aspects/processes -- 2.3.1.1 Embryogenesis -- 2.3.1.2 Branching morphogenesis -- 2.3.1.3 Stem cell niches and stem cell differentiation -- 2.3.1.4 Homeostasis -- 2.3.2 How systems work -- 2.3.2.1 ECM in nervous system development -- 2.3.2.2 Skeletal development -- 2.3.2.3 Skin development -- 2.4 ECM remodeling in regeneration and repair -- 2.4.1 Intervertebral disc regeneration -- 2.4.2 Wound healing -- 2.4.3 Bone remodeling and healing -- 2.4.4 CNS regeneration and repair -- 2.5 Conclusions -- References -- Chapter 3: Surface functionalization of biomaterials for bone tissue regeneration and repair -- 3.1 General introduction and chapter overview -- 3.2 Principles of surface biofunctionalization for bone repair -- 3.2.1 Mimicking bone ECM with peptides and proteins -- 3.2.1.1 Integrin signaling -- 3.2.1.2 Growth factor signaling -- 3.2.2 Ligands used for biofunctionalization -- 3.2.2.1 Limitations of proteins -- 3.2.2.2 Limitations of synthetic peptides -- 3.3 RGD peptidomimetics as surface coating molecules -- 3.3.1 Cyclic peptides and modifications of the peptide structure -- 3.3.2 Design of nonpeptidic integrin-binding ligands -- 3.3.3 Examples of surface functionalization with avß3- or a5ß1-selective peptidomimetics -- 3.4 Multifunctionality on biomaterials. , 3.4.1 Combining multiple biological cues-toward highly bioactive biomaterials -- 3.4.1.1 Multifunctional approaches (I): Improving cell adhesion -- 3.4.1.2 Multifunctional approaches (II): Mimicking the ECM microenvironment -- 3.4.1.3 Multifunctional approaches (III): Winning the race for the surface -- 3.4.2 Systems of presentation -- 3.4.2.1 Peptide mixtures -- 3.4.2.2 Peptide oligomers and constructs -- 3.4.2.3 Engineered protein fragments -- 3.4.2.4 Growth factor recruiting systems -- 3.4.2.5 Functionalized (antifouling) polymers -- 3.4.2.6 Functionalized drug-releasing polymers -- 3.4 Conclusions and future perspectives -- References -- Chapter 4: Bioengineered peptide-functionalized hydrogels for tissue regeneration and repair -- 4.1 Introduction -- 4.1.1 Structural and compositional features of the native extracellular matrix -- 4.2 Hydrogels as ECM mimics -- 4.2.1 Bioactive and bioinert hydrogels -- 4.3 Bioengineered hydrogels -- 4.3.1 Biofunctionalization of hydrogels with bioactive peptides -- 4.3.1.1 Hydrogel conjugation with integrin-binding peptides -- 4.3.1.2 Hydrogel conjugation with protease-sensitive peptides -- 4.3.1.3 Hydrogel conjugation with proangiogenic peptides -- 4.3.1.4 Hydrogel conjugation with differentiation-inducer peptides -- 4.3.1.5 Hydrogel conjugation with GAG-binding peptides -- 4.4 Balancing biochemical and biomechanical cues in hydrogel-based matrices -- 4.5 Dynamically switchable peptide-functionalized hydrogels -- 4.6 General conclusions and future directions -- Acknowledgments -- References -- Chapter 5: Collagen-based biomaterials for tissue regeneration and repair -- 5.1 Introduction -- 5.2 Structure and function of collagen -- 5.3 Manufacturing and fabrication of collagen-based biomaterials -- 5.3.1 Isolation of collagen -- 5.3.2 Freeze-drying -- 5.3.3 Electrospinning -- 5.3.4 3D bioprinting. , 5.3.5 Cross-linking -- 5.3.5.1 Dehydrothermal treatment -- 5.3.5.2 Ultraviolet radiation -- 5.3.5.3 Glutaraldehyde -- 5.3.5.4 Carbodiimides -- 5.3.5.5 Microbial transglutaminase -- 5.4 Functionalized collagen-based biomaterials for tissue regeneration -- 5.4.1 Composite scaffolds -- 5.4.2 Cell-based therapies -- 5.4.3 Growth factor and recombinant protein delivery -- 5.4.4 Gene-activated matrices -- 5.5 State of the art and future trends -- References -- Chapter 6: Fibrin biomaterials for tissue regeneration and repair -- 6.1 Introduction -- 6.2 Fibrin(ogen) structure -- 6.3 Fibrin polymerization -- 6.4 Overview of fibrin's role in promoting cell infiltration during wound repair -- 6.5 Fibrin-cell interactions -- 6.6 Impact of cells on fibrin network formation and properties -- 6.7 Fibrin and inflammation -- 6.8 Fibrin and angiogenesis -- 6.9 Overview of fibrin biomaterials and current clinical uses -- 6.10 Fibrin as a tissue sealant -- 6.11 Engineering the properties of fibrin networks -- 6.12 Mechanical modification of stiffness/elasticity -- 6.13 Modification of degradation properties -- 6.14 Modification with growth factors -- 6.15 Summary and future outlooks -- References -- Chapter 7: Fibrous protein-based biomaterials (silk, keratin, elastin, and resilin proteins) for tissue regeneration and repair -- 7.1 Introduction -- 7.2 Biopolymer-gels based on fibrous proteins: General considerations -- 7.3 Silk fibroin -- 7.3.1 Protein structure -- 7.3.2 Extraction and purification -- 7.3.3 Hydrogels formation -- 7.3.4 Applications in tissue repair and regeneration -- 7.4 Keratins -- 7.4.1 Protein structure -- 7.4.2 Extraction and purification -- 7.4.3 Hydrogel formation -- 7.4.4 Applications in tissue repair and regeneration -- 7.4.4.1 Nerve regeneration -- 7.4.4.2 Wound dressing -- 7.4.4.3 Hemostatic agent -- 7.4.4.4 Cartilage tissue engineering. , 7.4.4.5 Controlled drug delivery system -- 7.4.4.6 Cell culture systems -- 7.5 Elastin -- 7.5.1 Protein structure -- 7.5.2 Extraction and purification -- 7.5.3 Hydrogel formation -- 7.5.4 Application in tissue repair and regeneration -- 7.6 Resilin -- 7.6.1 Protein structure -- 7.6.2 Protein extraction and purification -- 7.6.3 Hydrogel formation -- 7.6.4 Application on tissue repair and regeneration -- 7.7 Final remarks and future perspectives -- References -- Further reading -- Chapter 8: Fabrication of nanofibers and nanotubes for tissue regeneration and repair -- 8.1 Introduction -- 8.2 Nanofibers from organic materials -- 8.2.1 Electrospinning -- 8.2.2 Self-assembly -- 8.2.3 Phase separation -- 8.2.4 Other processing techniques -- 8.3 Inorganic nanofibers -- 8.4 Nanotubes -- 8.5 Nanocomposites -- 8.6 Conclusions -- References -- Further reading -- Chapter 9: Peptide and protein printing for tissue regeneration and repair -- 9.1 Introduction -- 9.2 Contact printing technologies -- 9.2.1 Reactive microcontact printing -- 9.2.2 Supramolecular microcontact printing -- 9.2.3 Dip pen nanolithography -- 9.2.4 Polymer pen lithography -- 9.2.5 Transfer printing -- 9.3 Printing applications in biology and medicine -- 9.3.1 Biomaterial microarrays -- 9.3.2 ECM microarrays to control cell shape -- 9.3.3 Shape-induced stem cell differentiation -- 9.3.4 Printed arrays for neurons -- 9.3.5 Peptide arrays in cartilage research -- 9.3.6 Antiinflammation by printed micropatterns -- 9.3.7 Drug delivery from arrays -- 9.3.8 Biomembrane modeling -- 9.4 Conclusion and outlook -- Acknowledgments -- References -- Chapter 10: Self-assembling peptides and their application in tissue engineering and regenerative medicine -- 10.1 Introduction -- 10.2 Common secondary structure of proteins and peptides -- 10.2.1 α-Helix -- 10.2.2 Coiled-coil helix -- 10.2.3 ß-Sheet. , 10.2.4 ß-Hairpins.
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  • 2
    facet.materialart.
    Unbekannt
    PANGAEA
    In:  Supplement to: Range, P; Martins, M; Cabral, S; Pilò, D; Ben-Hamadou, R; Teodósio, M A; Leitão, F; Drago, Teresa; Oliveira, A P; Matias, D; ChÌcharo, L (2014): Relative sensitivity of soft-bottom intertidal macrofauna to increased CO2 and experimental stress. Marine Ecology Progress Series, 509, 153-170, https://doi.org/10.3354/meps10861
    Publikationsdatum: 2024-03-15
    Beschreibung: We used a controlled CO2 perturbation experiment to test hypotheses about changes in diversity, composition and structure of soft-bottom intertidal macrobenthic assemblages, under realistic and locally relevant scenarios of seawater acidification. Patches of undisturbed sediment were collected from 2 types of intertidal sedimentary habitat in the Ria Formosa coastal lagoon (South Portugal) and exposed to 2 levels of seawater acidification (pH reduced by 0.3 and 0.6 units) and 1 unmanipulated (control) level. After 75 d the assemblages differed significantly between the 2 types of sediment and between field controls and the ex situ treatments, but not among the 3 pH levels tested. The naturally high values of total alkalinity buffered seawater from the changes imposed on carbonate chemistry and may have contributed to offsetting acidification at the local scale. Observed differences on biota were strongly related to the organic matter content and grain-size of the sediments, particularly to the fractions of medium and coarse sand. Soft-bottom intertidal macrofauna was significantly affected by the stress of being held in an artificial environment, but not by CO2-induced seawater acidification. Given the previously observed variations in the sensitivities of marine organisms to seawater acidification, direct extrapolations of the present findings to different regions or other types of assemblages do not seem advisable. However, the contribution of ex situ studies to the assessment of ecosystem-level responses to environmental disturbances could generally be improved by incorporating adequate field controls in the experimental design.
    Schlagwort(e): Abra nitida; Abra prismatica; Abra tenuis; Abundance per area; Acteon tornatilis; Alkalinity, total; Alkalinity, total, standard error; Apohyale prevostii; Aragonite saturation state; Aragonite saturation state, standard error; Atylus swammerdami; Benthos; Bicarbonate ion; Biomass/Abundance/Elemental composition; Bittium sp.; Bulla striata; Calcite saturation state; Calcite saturation state, standard error; Calculated; Calculated using seacarb after Nisumaa et al. (2010); Calyptraea chinensis; Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard error; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cerastoderma edule; Cerastoderma glaucum; Cerithium vulgatum; Coast and continental shelf; Community composition and diversity; Containers and aquaria (20-1000 L or 〈 1 m**2); Crangon crangon; Cyclope pellucida; Date; Diogenes pugilator; Ensis siliqua; Entire community; Euphausia krohni; EXP; Experiment; Family; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Genus; Habitat; Haminoea hydatis; Individuals; Laboratory experiment; Lekanesphaera monodi; Liocarcinus arcuatus; Loripes lacteus; Lutraria lutraria; Melita palmata; Mesalia mesal; Metapenaeus monoceros; Nassarius cuvieri; Nassarius incrassatus; Nassarius nitidus; Nassarius pfeifferi; Nassarius pygmaeus; Nassarius reticulatus; North Atlantic; Nucula nucleus; Nucula sulcata; OA-ICC; Ocean Acidification International Coordination Centre; Pachygrapsus marmoratus; Pagurus sp.; Paphia aurea; Paphia rhomboides; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; Parvicardium exiguum; Peringia ulvae; pH; pH, standard error; Pholas dactylus; Potentiometric; Potentiometric titration; Replicate; Rissoa monodonta; Ruditapes decussatus; Salinity; Salinity, standard error; Scrobicularia plana; Soft-bottom community; Solen marginatus; Species; Spisula subtruncata; SW_Iberian_Peninsula; Taxon/taxa; Temperate; Temperature, water; Temperature, water, standard error; Treatment; Upogebia pusilla
    Materialart: Dataset
    Format: text/tab-separated-values, 11595 data points
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  • 3
    Publikationsdatum: 2024-03-15
    Beschreibung: Sites with naturally high CO2 conditions provide unique opportunities to forecast the vulnerability of coastal ecosystems to ocean acidification, by studying the biological responses and potential adaptations to this increased environmental variability. In this study, we investigated the bivalve Ervilia castanea in coastal sandy sediments at reference sites and at volcanic CO2 seeps off the Azores, where the pH of bottom waters ranged from average oceanic levels of 8.2, along gradients, down to 6.81, in carbonated seawater at the seeps. The bivalve population structure changed markedly at the seeps. Large individuals became less abundant as seawater CO2 levels rose and were completely absent from the most acidified sites. In contrast, small bivalves were most abundant at the CO2 seeps. We propose that larvae can settle and initially live in high abundances under elevated CO2 levels, but that high rates of post-settlement dispersal and/or mortality occur. Ervilia castanea were susceptible to elevated CO2 levels and these effects were consistently associated with lower food supplies. This raises concerns about the effects of ocean acidification on the brood stock of this species and other bivalve molluscs with similar life history traits.
    Schlagwort(e): Abundance per area; Alkalinity, total; Alkalinity, total, standard error; Animalia; Aragonite saturation state; Aragonite saturation state, standard error; Ash mass; Benthic animals; Benthos; Bicarbonate ion; Bicarbonate ion, standard error; Biomass/Abundance/Elemental composition; Calcification/Dissolution; Calcite saturation state; Calcite saturation state, standard error; Calcium carbonate; Calcium carbonate, standard error; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard error; Carbon, organic, total; Carbon, organic, total, standard error; Carbon/Nitrogen ratio; Carbon/Nitrogen ratio, standard error; Carbonate ion; Carbonate ion, standard error; Carbonate system computation flag; Carbon dioxide; Chlorophyll a; Chlorophyll a, standard error; CO2 vent; Coast and continental shelf; DATE/TIME; Dry mass; Ervilia castanea; Event label; EXP; Experiment; Faial; Field observation; Fucoxanthin; Fucoxanthin, standard error; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Granulometry; Granulometry, standard error; Hydroxide ion; Hydroxide ion, standard error; Identification; LATITUDE; LONGITUDE; Mollusca; Nitrogen, total; Nitrogen, total, standard error; North Atlantic; OA-ICC; Ocean Acidification International Coordination Centre; Organic matter; Organic matter, standard error; Other studied parameter or process; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Partial pressure of carbon dioxide (water) at sea surface temperature (wet air), standard error; Percentage; pH; pH, standard error; Pigments; Pigments, standard error; Potentiometric; Potentiometric titration; Registration number of species; Replicate; Salinity; Salinity, standard error; Sample code/label; Sao_Miguel; Single species; Site; Size; Species; Temperate; Temperature, water; Temperature, water, standard error; Type; Uniform resource locator/link to reference
    Materialart: Dataset
    Format: text/tab-separated-values, 5812 data points
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  • 4
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Analytical chemistry 50 (1978), S. 229-231 
    ISSN: 1520-6882
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    [S.l.] : American Institute of Physics (AIP)
    Journal of Applied Physics 89 (2001), S. 6680-6682 
    ISSN: 1089-7550
    Quelle: AIP Digital Archive
    Thema: Physik
    Notizen: We present experimental results on the growth and structure of Fe overlayers deposited on Cu84Al16(100) and discuss the correlation between the structural and magnetic properties of this system. Fe films 1–6 monolayers (ML) thick were grown under molecular beam epitaxy conditions onto the clean substrate at 160 K. Electron diffraction was applied to investigate the structure of the Fe films. The magnetic properties were investigated in situ by surface magneto-optical Kerr effect in the longitudinal geometry. Our results show that the onset of in-plane ferromagnetism around 3.5 ML of Fe coincides with structural changes that suggest a transformation within the Fe films from a fcc-like (100) to a bcc-like (110) structure with increasing Fe thickness, starting from 2.5 ML. © 2001 American Institute of Physics.
    Materialart: Digitale Medien
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  • 6
    ISSN: 1398-9995
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: The aim of this study was to investigate the role of immunoglobulin E (IgE) in the late phase reaction (LPR) of murine experimental asthma. Our model consisted of an implant of DNP-conjugated, heat-coagulated hen's egg white (DNP-EWI), followed 14 days later by an intratracheal challenge with aggregated DNP-ovalbumin. Airway inflammation was analyzed 48 h after challenge and compared with a similarly immunized group of mice with highly suppressed humoral response due to anti-μ and anti-δ antibody treatment. Total number of cells in the bronchoalveolar lavage (BAL) (with predominance of eosinophils) and EPO activity in the lung homogenate were increased in the DNP-EWI-immunized group compared with immunosuppressed or nonimmunized mice. However, the cellular infiltration and EPO activity observed in the immunosuppressed group were still significantly above those obtained in the nonimmunized group, indicating that inhibition of antibody production did not completely prevent the inflammatory manifestations in BAL and lung. Airway hyperresponsiveness to methacoline was obtained in DNP-EWI-immunized mice, but the respiratory mechanical parameters returned to normal levels in the immunosuppressed group. When these mice were reconstituted with monoclonal anti-DNP antibodies, only IgE, but not IgG1, restored lung inflammation and decreased the conductance of the respiratory system, therefore, increasing hyperresponsiveness. These results indicate that antibodies are not essential for induction of LPR in the lung. However, IgE enhances pulmonary inflammation and hyperresponsiveness.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Langmuir 5 (1989), S. 165-170 
    ISSN: 1520-5827
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Ltd
    Scandinavian journal of immunology 55 (2002), S. 0 
    ISSN: 1365-3083
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Toxoplasma gondii is an intracellular parasite whose life cycle may include the man as an intermediate host. Close to a billion people are infected with this parasite worldwide. Ocular lesions may occur in up to 25% of those individuals infected. The infection may occur intra-uterus, through the placenta when the mother is infected during pregnancy. The parasite may also infect adults after the ingestion of contaminated food products, most notably meats or water. We have shown that although congenital and post-natal (acquired) infection results in similar ocular lesions, the immunological mechanisms behind the development of disease are different. On the other hand, contrary to published data obtained in mice, we were unable to find evidence that the T. gondii express superantigen activity for human lymphocytes. Our findings are important because they suggest that superantigen activity is not important as a pathological mechanism in human disease. Our data also suggest that, whereas the ocular lesion caused by infection after birth is the result of an excessive or dysfunctional immune response, the lesions caused by congenital infection may be due to a lack of an appropriate response to the parasite.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Science Ltd
    Clinical & experimental allergy 35 (2005), S. 0 
    ISSN: 1365-2222
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Background We have recently isolated two distinct components from Ascaris suum adult worms with different effects on the immune system: the allergenic protein of A. suum (APAS-3), which induces IgE antibody production, and suppressive protein of A. suum (PAS-1), which inhibits humoral and cellular immune responses induced by unrelated antigens. In this study, we investigated the immunomodulatory effect of PAS-1 on a murine model of asthma induced by APAS-3.Methods BALB/c mice were immunized twice with APAS-3 or APAS-3 plus PAS-1 by the intraperitoneal and subcutaneous route (on days 0 and 7) and challenged twice with the same antigens intranasally (days 14 and 21). Two days after the last challenge, the allergic airway inflammation was evaluated by cellular migration, eosinophil peroxidase (EPO) activity, cytokine and chemokine production and pulmonary mechanical parameters.Results The allergenic properties of APAS-3 were confirmed by the stimulation of anaphylactic IgE and IgG1 antibody production and eosinophilic airway inflammation and hyper-responsiveness. On the other hand, PAS-1-treated mice showed a marked suppression of cellular migration and EPO activity that correlated well with a significant reduction in the levels of IL-4, IL-5, eotaxin and RANTES in the bronchoalveolar lavage (BAL) fluid. In contrast, considerable amounts of IL-10 were observed in the BAL fluid of PAS-1-treated mice. Airway hyper-responsiveness was obtained in APAS-3-immunized mice, but the conductance of the respiratory system was restored to normal values in the presence of PAS-1.Conclusion These results indicate that A. suum allergenic protein APAS-3 induces a T helper 2-type immune response and, consequently, eosinophilic airway inflammation and hyper-responsiveness. Moreover, the modulatory protein PAS-1 has a marked suppressive effect on this response, and the inhibition of cytokine (IL-4, IL-5) and chemokine (eotaxin and RANTES) release, probably because of the presence of IL-10, may contribute to this effect.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
    ISSN: 1365-2222
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Medizin
    Notizen: Background The site and distribution of inflammation in the airways of asthmatic patients has been largely investigated. Inflammatory cells are distributed in both large and small airways in asthma. It has been demonstrated that distal lung inflammation in asthma may significantly contribute to the pathophysiology of the disease. The upper airways have also been implicated in the overall asthmatic inflammation. Although it is now accepted that lung inflammation is not restricted to the intrapulmonary airways in asthma, little is known about cell distribution in the other lung compartments and their relation to the intrapulmonary airways.Objective We aimed to map the inflammatory process in fatal asthma (FA), from the upper airways to the lung parenchyma.Methods Eosinophil, neutrophil, mast cell and lymphocyte content were determined in nasal mucosa, the trachea, intrapulmonary airways and parenchyma (peribronchiolar and distal) of 20 patients with FA and 10 controls.Results Eosinophil content was higher in all studied areas in FA compared with controls (P〈0.02). Mast cell content was higher in the outer area of larger airways, small membranous bronchioles and in peribronchiolar parenchyma of FA compared with controls (P〈0.04). CD3+, CD4+and CD20+cells showed increased content in FA intrapulmonary airways compared with controls (P〈0.05). There was a positive correlation between CD4+cell content in nasal mucosa and larger airways in asthmatics. Increased neutrophil content was observed only in peribronchiolar parenchyma of FA (P=0.028).Conclusion Eosinophils present a widespread distribution within the respiratory tract in FA, from the nasal mucosa to the distal lung. The outer wall of small membranous bronchioles is the main site of inflammatory changes in FA. There is a localized distribution of alveolar inflammation at the peribronchiolar region for mast cells and neutrophils. Our findings provide further evidence of the importance of the lung periphery in the pathophysiology of FA.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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