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类风湿性滑膜炎和滑液中α4β7整合素的差异表达。一种纤连蛋白和血管细胞黏附分子-1的新型受体。

Differential expression in rheumatoid synovium and synovial fluid of alpha 4 beta 7 integrin. A novel receptor for fibronectin and vascular cell adhesion molecule-1.

作者信息

Lazarovits A I, Karsh J

机构信息

John P. Robarts Research Institute, University Hospital, London, Ontario, Canada.

出版信息

J Immunol. 1993 Dec 1;151(11):6482-9.

PMID:7504021
Abstract

T lymphocyte adhesion to vascular endothelium plays an important role in the immunopathogenesis of rheumatoid arthritis. The migration of T lymphocytes into the synovium is mediated by a variety of adhesion molecules, notably the integrins. We have prepared Act I, a murine mAb that identifies a novel integrin termed alpha 4 beta 7. The natural ligands for alpha 4 beta 7 are vascular cell adhesion molecule-1 and fibronectin; both molecules are up-regulated in the rheumatoid synovium. We investigated the expression of alpha 4 beta 7 in the three compartments of rheumatoid arthritis, the peripheral blood, synovial fluid, and synovial membrane, utilizing the FACS and immunoperoxidase microscopy of frozen tissues. The results of our experiments show a striking differential expression of alpha 4 beta 7 integrin in rheumatoid arthritis. Sixty-two percent of synovial membrane T cells expressed high density alpha 4 beta 7, in contrast to only 4.7% of synovial fluid and 9.1% of PBL. These data suggest that the expression of alpha 4 beta 7 integrin may provide a mechanism whereby certain T cells adhere to rheumatoid synovium while others remain in the synovial fluid. The augmented expression of alpha 4 beta 7 in the synovial membrane T cells may contribute to the development and perpetuation of rheumatoid arthritis.

摘要

T淋巴细胞与血管内皮的黏附在类风湿关节炎的免疫发病机制中起重要作用。T淋巴细胞向滑膜的迁移由多种黏附分子介导,尤其是整合素。我们制备了Act I,一种识别名为α4β7的新型整合素的鼠单克隆抗体。α4β7的天然配体是血管细胞黏附分子-1和纤连蛋白;这两种分子在类风湿滑膜中均上调。我们利用流式细胞术(FACS)和冷冻组织的免疫过氧化物酶显微镜技术,研究了α4β7在类风湿关节炎的三个部位,即外周血、滑液和滑膜中的表达。我们的实验结果显示,α4β7整合素在类风湿关节炎中存在显著的差异表达。62%的滑膜T细胞表达高密度的α4β7,相比之下,滑液中只有4.7%,外周血淋巴细胞(PBL)中只有9.1%。这些数据表明,α4β7整合素的表达可能提供了一种机制,使某些T细胞能够黏附于类风湿滑膜,而其他T细胞则留在滑液中。滑膜T细胞中α4β7表达的增加可能有助于类风湿关节炎的发展和持续存在。

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