UID:
edocfu_9958058463402883
Format:
1 online resource (98 p.)
ISBN:
1-61504-166-4
Series Statement:
Integrated systems physiology : from molecule to function, bk. #8
Content:
The microcirculation is highly responsive to, and a vital participant in, the inflammatory response. All segments of the microvasculature (arterioles, capillaries, and venules) exhibit characteristic phenotypic changes during inflammation that appear to be directed toward enhancing the delivery of inflammatory cells to the injured/infected tissue, isolating the region from healthy tissue and the systemic circulation, and setting the stage for tissue repair and regeneration. The best characterized responses of the microcirculation to inflammation include impaired vasomotor function, reduced capillary perfusion, adhesion of leukocytes and platelets, activation of the coagulation cascade, and enhanced thrombosis, increased vascular permeability, and an increase in the rate of proliferation of blood and lymphatic vessels. A variety of cells that normally circulate in blood (leukocytes, platelets) or reside within the vessel wall (endothelial cells, pericytes) or in the perivascular space (mast cells, macrophages) are activated in response to inflammation. The activation products and chemical mediators released from these cells act through different well-characterized signaling pathways to induce the phenotypic changes in microvessel function that accompany inflammation. Drugs that target a specific microvascular response to inflammation, such as leukocyte-endothelial cell adhesion or angiogenesis, have shown promise in both the preclinical and clinical studies of inflammatory disease. Future research efforts in this area will likely identify new avenues for therapeutic intervention in inflammation.
Note:
Part of: Colloquium digital library of life sciences.
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Series from website.
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1. Introduction --
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2. Historical perspectives --
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3. Anatomical considerations -- Microvascular unit -- Arterioles -- Capillaries -- Venules -- Vessel wall components -- Endothelial cells -- Vascular smooth muscle -- Pericytes -- Perivascular auxiliary cells -- Mast cells -- Macrophages -- Fibroblasts --
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4. Impaired vasomotor responses -- Blood flow changes -- Endothelium-dependent vasodilation --
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5. Capillary perfusion --
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6. Angiogenesis -- Relevance to inflammation -- Mediators of the angiogenic response -- Vascular endothelial cell growth factor -- Cytokines and chemokines -- Reactive oxygen and nitrogen species -- Lymphangiogenesis --
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7. Leukocyte-endothelial cell adhesion -- Adhesion molecules -- Intraorgan heterogeneity of adhesion -- Selectins -- Endothelial cells immunoglobulin-like adhesion molecules -- Leukocyte integrins -- Chemical mediators -- Pro-adhesive mediators -- Anti-adhesive mediators -- Role of hydrodynamic forces -- Cytotoxicity of adherent leukocytes --
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8. Platelet-vessel wall interactions -- Platelet activation: mechanisms and consequences -- Platelet-endothelial adhesion -- Platelet-leukocyte adhesion -- Platelet-leukocyte aggregates --
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9. Coagulation and thrombosis -- Interdependence of coagulation and inflammation -- Inflammation-induced microvascular thrombosis: site-specific responses -- Chemical mediators of inflammation-enhanced thrombosis -- Reactive oxygen and nitrogen species --
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10. Endothelial barrier dysfunction -- Site of inflammation-induced barrier failure -- Role of circulating blood cells -- Leukocytes -- Platelets -- Role of perivascular cells -- Reactive oxygen and nitrogen species --
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Epilogue -- References.
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Also available in print.
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English
Additional Edition:
ISBN 1-61504-165-6
Language:
English
DOI:
10.4199/C00013ED1V01Y201006ISP008
