Shaw S K, Brenner M B
Division of Rheumatology and Immunology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Semin Immunol. 1995 Oct;7(5):335-42. doi: 10.1016/1044-5323(95)90014-4.
Lymphocytes recirculate extensively throughout the body and then localize in tissues and lymphoid organs. This is accomplished by an array of adhesion molecules on lymphocytes and counter-receptors on the vascular endothelium, extracellular matrix and the epithelium. Recent studies have identified several of the specific molecular interactions that mediate lymphocyte trafficking. Lymphocytes expressing alpha 4 beta 7 home to the intestine through recognition of the mucosal addressin cell adhesion molecule-1 (MAdCAM-1) expressed on Peyer's patch high endothelial venules. T cells in nearly all mucosal epithelial sites express the alpha E beta 7 integrin which has been shown to mediate lymphocyte binding to epithelial cell E-cadherin. Thus, members of the B7 subfamily of integrins, alpha E beta 7 and alpha 4 beta 7, and their counter-receptors, are believed to play key roles in directing lymphocyte traffic to and retention in mucosal organs.
淋巴细胞在全身广泛循环,然后定位于组织和淋巴器官。这是通过淋巴细胞上一系列粘附分子以及血管内皮、细胞外基质和上皮细胞上的反受体来实现的。最近的研究已经确定了几种介导淋巴细胞运输的特定分子相互作用。表达α4β7的淋巴细胞通过识别派尔集合淋巴结高内皮微静脉上表达的黏膜地址素细胞粘附分子-1(MAdCAM-1)而归巢至肠道。几乎所有黏膜上皮部位的T细胞都表达αEβ7整合素,该整合素已被证明可介导淋巴细胞与上皮细胞E-钙粘蛋白的结合。因此,整合素B7亚家族的成员αEβ7和α4β7及其反受体,被认为在引导淋巴细胞向黏膜器官运输并滞留于其中发挥关键作用。