Streeter P R, Rouse B T, Butcher E C
Department of Pathology, Stanford University School of Medicine, California 94305.
J Cell Biol. 1988 Nov;107(5):1853-62. doi: 10.1083/jcb.107.5.1853.
The tissue localization or "homing" of circulating lymphocytes is directed in part by specialized vessels that define sites of lymphocyte exit from the blood. In peripheral lymph nodes, mucosal lymphoid tissues (Peyer's patches and appendix), and sites of chronic inflammation, for example, lymphocytes leave the blood by adhering to and migrating between those endothelial cells lining postcapillary high endothelial venules (HEV). Functional analyses of lymphocyte interactions with HEV have shown the lymphocytes can discriminate between HEV in different tissues, indicating that HEV express tissue-specific determinants or address signals for lymphocyte recognition. We recently described such a tissue-specific "vascular addressin" that is selectively expressed by endothelial cells supporting lymphocyte extravasation into mucosal tissues and that appears to be required for mucosa-specific lymphocyte homing (Streeter, P. R., E. L. Berg, B. N. Rouse, R. F. Bargatze, and E. C. Butcher. 1988. Nature (Lond.). 331:41-46). Here we document the existence and tissue-specific distribution of a distinct HEV differentiation antigen. Defined by monoclonal antibody MECA-79, this antigen is expressed at high levels on the lumenal surface and in the cytoplasm of HEV in peripheral lymph nodes. By contrast, although MECA-79 stains many HEV in the mucosal Peyer's patches, expression in most cases is restricted to the perivascular or ablumenal aspect of these venules. In the small intestine lamina propria, a mucosa-associated site that supports the extravasation of lymphocytes, venules do not stain with MECA-79. Finally, we demonstrate that MECA-79 blocks binding of both normal lymphocytes and a peripheral lymph node-specific lymphoma to peripheral lymph node HEV in vitro and that it also inhibits normal lymphocyte homing to peripheral lymph nodes in vivo without significantly influencing lymphocyte interactions with Peyer's patch HEV in vitro or in vivo. Thus, MECA-79 defines a novel vascular addressin involved in directing lymphocyte homing to peripheral lymph nodes.
循环淋巴细胞的组织定位或“归巢”部分是由特定血管引导的,这些血管确定了淋巴细胞从血液中流出的部位。例如,在周围淋巴结、黏膜淋巴组织(派尔集合淋巴结和阑尾)以及慢性炎症部位,淋巴细胞通过黏附于毛细血管后高内皮微静脉(HEV)的内皮细胞并在这些内皮细胞之间迁移而离开血液。淋巴细胞与HEV相互作用的功能分析表明,淋巴细胞能够区分不同组织中的HEV,这表明HEV表达组织特异性决定簇或淋巴细胞识别的地址信号。我们最近描述了一种这样的组织特异性“血管地址素”,它由支持淋巴细胞渗入黏膜组织的内皮细胞选择性表达,并且似乎是黏膜特异性淋巴细胞归巢所必需的(斯特里特,P.R.,E.L.伯格,B.N.劳斯,R.F.巴尔加茨,和E.C.布彻。1988年。《自然》(伦敦)。331:41 - 46)。在这里,我们记录了一种独特的HEV分化抗原的存在及其组织特异性分布。由单克隆抗体MECA - 79定义,这种抗原在周围淋巴结的HEV腔面和细胞质中高水平表达。相比之下,尽管MECA - 79可染色黏膜派尔集合淋巴结中的许多HEV,但在大多数情况下,表达仅限于这些微静脉的血管周围或非腔面。在小肠固有层,一个支持淋巴细胞渗出的黏膜相关部位,微静脉不被MECA - 79染色。最后,我们证明MECA - 79在体外可阻断正常淋巴细胞和外周淋巴结特异性淋巴瘤与外周淋巴结HEV的结合,并且它在体内也抑制正常淋巴细胞归巢至外周淋巴结,而不会显著影响淋巴细胞在体外或体内与派尔集合淋巴结HEV的相互作用。因此,MECA - 79定义了一种参与引导淋巴细胞归巢至外周淋巴结的新型血管地址素。