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α4β7整合素介导淋巴细胞与黏膜血管地址素MAdCAM-1的结合。

Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1.

作者信息

Berlin C, Berg E L, Briskin M J, Andrew D P, Kilshaw P J, Holzmann B, Weissman I L, Hamann A, Butcher E C

机构信息

Department of Pathology, Stanford University, California 94305.

出版信息

Cell. 1993 Jul 16;74(1):185-95. doi: 10.1016/0092-8674(93)90305-a.

Abstract

The mucosal vascular addressin, MAdCAM-1, is an immunoglobulin superfamily adhesion molecule for lymphocytes that is expressed by mucosal venules and helps direct lymphocyte traffic into Peyer's patches (PP) and the intestinal lamina propria. We demonstrate that the lymphocyte integrin alpha 4 beta 7, also implicated in homing to PP, is a receptor for MAdCAM-1. Certain antibodies to alpha 4 and beta 7 integrin chains but not to the beta 2 integrin LFA-1 inhibit lymphocyte binding to purified MAdCAM-1 and to MAdCAM-1 transfectants. Lymph node lymphocytes, alpha 4 beta 7+ TK1 lymphoma cells, and a beta 7-transfected variant of an alpha 4+ B cell line, 38C13, bind constitutively to MAdCAM-1. Binding is enhanced by Mn(++)-induced integrin activation. The related integrin alpha 4 beta 1 supports efficient binding to VCAM-1 but not to MAdCAM-1, even after integrin activation, indicating that MAdCAM-1 is a preferential ligand for alpha 4 beta 7. Alpha 4 beta 7 can also bind VCAM-1, but this requires greater integrin activation than binding to MAdCAM-1. The findings imply a selective role for the interaction of alpha 4 beta 7 and MAdCAM-1 lymphocyte in homing to mucosal sites.

摘要

黏膜血管地址素MAdCAM-1是一种淋巴细胞免疫球蛋白超家族黏附分子,由黏膜微静脉表达,有助于引导淋巴细胞进入派尔集合淋巴结(PP)和肠固有层。我们证明,同样参与归巢至PP的淋巴细胞整合素α4β7是MAdCAM-1的受体。某些针对α4和β7整合素链而非β2整合素LFA-1的抗体可抑制淋巴细胞与纯化的MAdCAM-1及MAdCAM-1转染细胞的结合。淋巴结淋巴细胞、α4β7+ TK1淋巴瘤细胞以及α4+ B细胞系38C13的β7转染变体可组成性地与MAdCAM-1结合。锰离子(Mn++)诱导的整合素激活可增强这种结合。相关整合素α4β1即使在整合素激活后也能有效结合血管细胞黏附分子-1(VCAM-1),但不能结合MAdCAM-1,这表明MAdCAM-1是α4β7的优先配体。α4β7也能结合VCAM-1,但这比结合MAdCAM-1需要更强的整合素激活。这些发现表明α4β7与MAdCAM-1相互作用在淋巴细胞归巢至黏膜部位中具有选择性作用。

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