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活化的T细胞在跨内皮迁移过程中获得内皮细胞表面决定簇。

Activated T cells acquire endothelial cell surface determinants during transendothelial migration.

作者信息

Brezinschek R I, Oppenheimer-Marks N, Lipsky P E

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75235, USA.

出版信息

J Immunol. 1999 Feb 1;162(3):1677-84.

PMID:9973429
Abstract

Activated T cells acquire endothelial cell (EC) plasma membrane constituents during transendothelial migration. This was assessed using an in vitro model system in which human peripheral blood CD4+ T cells migrated through confluent monolayers of HUVEC. Flow cytometry of migrated CD4+ T cells demonstrated that activated, but not resting, T cells acquired a variety of endothelial surface determinants, including CD31, CD49d, CD54, CD61, and CD62E. The extracellular domains of these molecules were detected on migrated T cells with mAbs, including those directed to the ligand-binding regions. A number of approaches were employed to document that the acquisition of these molecules was uniquely accomplished by activated T cells and clearly involved transfer from both resting and TNF-alpha-activated EC. Acquisition of endothelial markers by activated T cells occurred as part of the transfer of membrane components, as migrating T cells acquired EC membranes prelabeled with the lipophilic dye, 3,3'-dihexadecyloxacarbocyanine perchlorate (DiOC-16), along with EC surface proteins. Thus, during transendothelial migration, activated T cells acquire endothelial membrane components, and as a result may deliver them to perivascular sites.

摘要

活化的T细胞在跨内皮迁移过程中获得内皮细胞(EC)的质膜成分。这是通过体外模型系统进行评估的,在该系统中,人外周血CD4+ T细胞穿过人脐静脉内皮细胞(HUVEC)的汇合单层。对迁移后的CD4+ T细胞进行流式细胞术分析表明,活化的而非静息的T细胞获得了多种内皮表面决定簇,包括CD31、CD49d、CD54、CD61和CD62E。用单克隆抗体(mAb)在迁移后的T细胞上检测到了这些分子的胞外结构域,包括那些针对配体结合区域的抗体。采用了多种方法来证明这些分子的获得是活化T细胞特有的过程,并且明确涉及来自静息和肿瘤坏死因子-α(TNF-α)活化的EC的转移。活化T细胞获得内皮标志物是膜成分转移的一部分,因为迁移的T细胞在获得EC表面蛋白的同时,还获得了用亲脂性染料3,3'-二己基氧杂羰花青高氯酸盐(DiOC-16)预标记的EC膜。因此,在跨内皮迁移过程中,活化的T细胞获得内皮膜成分,结果可能将它们递送至血管周围部位。

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