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Immunolocalization of extracellular matrix proteins and integrins in sarcoid lymph nodes
Authors:K Shigehara  Noriharu Shijubo  Michio Hirasawa  Shosaku Abe  Toshimitsu Uede
Institution:(1) Third Department of Internal Medicine, Sapporo Medical University School of Medicine, South-1, West-16, Chuo-ku, Sapporo, 060, Japan, Tel.: (+81)-11-611-2111, ext. 3239, Fax: (+81)-11-613-1543, JP;(2) Section of Immunopathogenesis, Institute of Immunological Science, Hokkaido University, Sapporo, Japan, JP
Abstract: To improve our understanding of the role of extracellular matrix (ECM) proteins and integrins during the processes of granuloma formation in sarcoidosis, we examined the distribution of ECM proteins and the expression of integrins in sarcoid lymph nodes by immunohistochemical methods. We also examined the expression of transforming growth factor-β1 (TGF-β1), which is one of major regulators for synthesis of ECM proteins. Most ECM proteins were detected in the periphery of the granulomas in a concentric pattern, and fibronectin was diffusely detected from an early to a regressive stage. Compared with normal lymph nodes, most β1-integrin subfamilies (α1, α4, α5 and α6) were more strongly expressed on lymphocytes around the granulomas. Epithelioid cells exhibited strong expression of the α5 molecule. Fibroblasts exhibited the expression of the α2 and α5 molecules surrounding ECM proteins. The α5β1 molecule had a distribution similar to that of fibronectin. TGF-β1 was detected in epithelioid cells throughout the various evolutional stages and its expression was especially marked in mature granulomas. Interaction of fibronectin and the α5β1 molecule may have an important role in the process of formation of sarcoid granuloma. The expression of TGF-β1 may be involved in the regression of sarcoid granuloma by initiating fibrosis and atrophy of epithelioid cells. Received: 2 December 1997 / Accepted: 19 February 1998
Keywords:  Adhesion molecule  Extracellular matrix proteins  Transforming growth factor-β  1  Granuloma formation and regression  Sarcoidosis
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