Rappl Gunter, Schrama David, Hombach Andreas, Meuer Eva Katharina, Schmidt Annette, Becker Jürgen C, Abken Hinrich
Tumorgenetics, Department of Internal Medicine I, University of Cologne, Cologne, Germany.
Rejuvenation Res. 2008 Jun;11(3):543-56. doi: 10.1089/rej.2007.0612.
CD7(-) T cells constitute a distinct subset within the CD4(+) and CD8(+) T cell populations; their developmental and functional relationship to the majority of CD7(+) T cells, however, remained so far unresolved. We here elucidate that CD7(-) cells represent aging T cells in late memory cell development characterized by a high activation threshold, low effector capacities, and high sensitivity to activation-induced cell death (AICD). In this regard, CD7(-) T cells highly express killer cell lectin-like receptor G1 (KLRG-1), harbor telomeres of shorter lengths, a decreased telomerase expression per cell, and less amounts of T cell receptor rearrangement excision circles (TRECs) compared to CD7(+) cells. CD7(-) T cells are generated in vitro from naive CD7(+) T cells upon repetitive TCR/CD28 engagement, a process that is unidirectional and requires multiple cell divisions. Consequently, clonal expansions of CD7(-) T cells in vivo are less frequent than of CD7(+) T cells, the former can be traced back to those of CD7(+) T cells.
CD7(-) T细胞在CD4(+)和CD8(+) T细胞群体中构成一个独特的亚群;然而,它们与大多数CD7(+) T细胞在发育和功能上的关系至今仍未解决。我们在此阐明,CD7(-)细胞代表晚期记忆细胞发育中的衰老T细胞,其特征为激活阈值高、效应能力低以及对激活诱导的细胞死亡(AICD)高度敏感。在这方面,与CD7(+)细胞相比,CD7(-) T细胞高表达杀伤细胞凝集素样受体G1(KLRG-1),端粒长度较短,每个细胞的端粒酶表达降低,且T细胞受体重排切除环(TREC)的量较少。CD7(-) T细胞在体外由幼稚CD7(+) T细胞经反复TCR/CD28结合产生,这一过程是单向的,且需要多次细胞分裂。因此,CD7(-) T细胞在体内的克隆扩增比CD7(+) T细胞少见,前者可追溯到CD7(+) T细胞的克隆扩增。