首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Cloning and expression of mouse integrin beta p(beta 7): a functional role in Peyers patch-specific lymphocyte homing.
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Cloning and expression of mouse integrin beta p(beta 7): a functional role in Peyers patch-specific lymphocyte homing.

机译:小鼠整联蛋白βp(beta 7)的克隆和表达:在派伊尔的修补程序特定的淋巴细胞归巢中的功能作用。

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摘要

Lymphocytes express integrin receptors, termed lymphocyte Peyer's patch high endothelial venule (HEV) adhesion molecules (LPAMs), that mediate their organ-specific adhesion to specialized HEVs found in mucosal lymphoid organs (Peyer's patches). LPAM-1 consists of a murine integrin alpha 4 noncovalently associated with integrin beta p. Here, we describe the cloning and expression of a mouse cDNA encoding beta p, which is an 806-amino acid transmembrane glycoprotein. The genomic Southern blot analysis indicates that beta p is the murine homologue of human beta 7. The function of alpha 4 beta 7 as a Peyer's patch-specific adhesion molecule was tested directly by expression of the murine beta 7 cDNA in an alpha 4+ beta 7-B-cell line or coexpression of the alpha 4 and beta 7 cDNAs in an alpha 4-beta 7-T-cell line. The transfected cells exhibited a new Peyer's patch-specific adhesive phenotype that could be specifically blocked by monoclonal antibodies against alpha 4 and beta 7. Moreover, an anti-beta 7 monoclonal antibody specifically blocked binding of normal lymphocytes to Peyer's patch HEV but did not inhibit their binding to peripheral lymph node HEVs, indicating that beta 7 is a unique component of the Peyer's patch-specific homing receptor.
机译:淋巴细胞表达整联蛋白受体,称为淋巴细胞Peyer's膜高内皮小静脉(HEV)粘附分子(LPAM),介导其器官特异性粘附至在粘膜淋巴器官中发现的特化HEV(Peyer's补丁)。 LPAM-1由与整联蛋白beta p非共价结合的鼠整联蛋白alpha 4组成。在这里,我们描述了编码beta的小鼠cDNA的克隆和表达,beta p是806个氨基酸的跨膜糖蛋白。基因组Southern印迹分析表明,βp是人类β7的鼠源同源物。直接通过在α4+ beta中表达鼠β7 cDNA来测试α4 beta 7作为派伊尔斑块特异性粘附分子的功能。 7-B细胞系或在α4-β7-T细胞系中共表达α4和β7 cDNA。转染的细胞表现出一种新的Peyer's特异性粘附表型,可以被针对α4和beta 7的单克隆抗体特异性阻断。此外,抗β7单克隆抗体可以特异性阻断正常淋巴细胞与Peyer's斑块HEV的结合,但不能抑制它们与外周淋巴结HEV的结合,表明β7是派伊尔斑块特异性归巢受体的独特组成部分。

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