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细胞间黏附分子-1(ICAM-1)共刺激靶细胞以促进抗原呈递。

ICAM-1 co-stimulates target cells to facilitate antigen presentation.

作者信息

Lebedeva Tatiana, Dustin Michael L, Sykulev Yuri

机构信息

Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

Curr Opin Immunol. 2005 Jun;17(3):251-8. doi: 10.1016/j.coi.2005.04.008.

Abstract

Adhesion molecules are known to mediate cell-cell interactions, particularly those between T cells and antigen-presenting or target cells. Recent studies identified ICAM-1 as a co-stimulatory ligand that binds to lymphocyte function associated antigen-1 (LFA-1), thereby promoting the activation of T cells. As ICAM-1 is expressed on virtually any cell, it becomes a crucial molecule for the activation of CD8(+) T cells in the absence of co-stimulation provided by CD80 and CD86 molecules. In addition, ICAM-1 might function as cell-surface receptor, capable of initiating intracellular signaling. ICAM-1 is associated with other cell molecules, including MHC-I proteins, and our recent data show that productive engagement of ICAM-1 on target cells leads to recruitment of the MHC-I proteins to the contact area and enhances presentation of cognate peptide MHC-I complexes to cytotoxic T cells.

摘要

已知黏附分子可介导细胞间相互作用,尤其是T细胞与抗原呈递细胞或靶细胞之间的相互作用。最近的研究确定细胞间黏附分子-1(ICAM-1)是一种共刺激配体,它与淋巴细胞功能相关抗原-1(LFA-1)结合,从而促进T细胞的激活。由于ICAM-1几乎在任何细胞上都有表达,在缺乏由CD80和CD86分子提供的共刺激的情况下,它成为激活CD8(+) T细胞的关键分子。此外,ICAM-1可能作为细胞表面受体,能够启动细胞内信号传导。ICAM-1与其他细胞分子相关,包括MHC-I蛋白,我们最近的数据表明,靶细胞上ICAM-1的有效结合会导致MHC-I蛋白募集到接触区域,并增强同源肽MHC-I复合物向细胞毒性T细胞的呈递。

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