Lebedeva Tatiana, Dustin Michael L, Sykulev Yuri
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
Curr Opin Immunol. 2005 Jun;17(3):251-8. doi: 10.1016/j.coi.2005.04.008.
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.
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。