Wells F B, Gahm S J, Hedrick S M, Bluestone J A, Dent A, Matis L A
Biological Carcinogenesis and Development Program, Program Resources, Inc./DynCorp, NCI-Frederick Cancer Research and Development Center, MD 21701-0201.
Science. 1991 Aug 23;253(5022):903-5. doi: 10.1126/science.1831565.
The alpha beta and gamma delta T cell receptors for antigen (TCR) delineate distinct T cell populations. TCR alpha beta-bearing thymocytes must be positively selected by binding of the TCR to major histocompatibility complex (MHC) molecules on thymic epithelium. To examine the requirement for positive selection of TCR gamma delta T cells, mice bearing a class I MHC-specific gamma delta transgene (Tg) were crossed to mice with disrupted beta 2 microglobulin (beta 2M) genes. The Tg+beta 2M- (class I MHC-) offspring had Tg+ thymocytes that did not proliferate to antigen or Tg-specific monoclonal antibody and few peripheral Tg+ cells. This is evidence for positive selection within the gamma delta T cell subset.
用于识别抗原的αβ和γδT细胞受体(TCR)划分出不同的T细胞群体。携带TCRαβ的胸腺细胞必须通过TCR与胸腺上皮细胞上的主要组织相容性复合体(MHC)分子结合而进行阳性选择。为了研究γδT细胞阳性选择的需求,将携带I类MHC特异性γδ转基因(Tg)的小鼠与β2微球蛋白(β2M)基因被破坏的小鼠进行杂交。Tg+β2M-(I类MHC-)后代有Tg+胸腺细胞,这些细胞不会对抗原或Tg特异性单克隆抗体发生增殖反应,且外周Tg+细胞很少。这是γδT细胞亚群内阳性选择的证据。