Fibulin-5, an integrin-binding matricellular protein: its function in development and disease
Autor: | Rolf A. Brekken, Marie K. Schluterman, Hiromi Yanagisawa |
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Rok vydání: | 2009 |
Předmět: |
Pathology
medicine.medical_specialty Angiogenesis Integrin Elastic fiber assembly Biochemistry Extracellular matrix 03 medical and health sciences 0302 clinical medicine medicine Fibronectin Molecular Biology Tissue homeostasis Cutis laxa 030304 developmental biology Integrin binding Thrombospondin 0303 health sciences Tumor biology Matricellular protein ROS Cell Biology 3. Good health Fibulin Cell biology 030220 oncology & carcinogenesis biology.protein Research Article Elastic fibers |
Zdroj: | Journal of Cell Communication and Signaling |
ISSN: | 1873-961X 1873-9601 |
Popis: | Interactions between the extracellular matrix (ECM) and cells are critical in embryonic development, tissue homeostasis, physiological remodeling, and tumorigenesis. Matricellular proteins, a group of ECM components, mediate cell-ECM interactions. One such molecule, Fibulin-5 is a 66-kDa glycoprotein secreted by various cell types, including vascular smooth muscle cells (SMCs), fibroblasts, and endothelial cells. Fibulin-5 contributes to the formation of elastic fibers by binding to structural components including tropoelastin and fibrillin-1, and to cross-linking enzymes, aiding elastic fiber assembly. Mice deficient in the fibulin-5 gene (Fbln5) exhibit systemic elastic fiber defects with manifestations of loose skin, tortuous aorta, emphysematous lung and genital prolapse. Although Fbln5 expression is down-regulated after birth, following the completion of elastic fiber formation, expression is reactivated upon tissue injury, affecting diverse cellular functions independent of its elastogenic function. Fibulin-5 contains an evolutionally conserved arginine-glycine-aspartic acid (RGD) motif in the N-terminal region, which mediates binding to a subset of integrins, including alpha5beta1, alphavbeta3, and alphavbeta5. Fibulin-5 enhances substrate attachment of endothelial cells, while inhibiting migration and proliferation in a cell type- and context-dependent manner. The antagonistic function of fibulin-5 in angiogenesis has been demonstrated in vitro and in vivo; fibulin-5 may block angiogenesis by inducing the anti-angiogenic molecule thrompospondin-1, by antagonizing VEGF(165)-mediated signaling, and/or by antagonizing fibronectin-mediated signaling through directly binding and blocking the alpha5beta1 fibronectin receptor. The overall effect of fibulin-5 on tumor growth depends on the balance between the inhibitory property of fibulin-5 on angiogenesis and the direct effect of fibulin-5 on proliferation and migration of tumor cells. However, the effect of tumor-derived versus host microenvironment-derived fibulin-5 remains to be evaluated. |
Databáze: | OpenAIRE |
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