Baird A M, Lucas J A, Berg L J
Department of Pathology, University of Massachusetts Medical School, Worcester 01655, USA.
J Immunol. 2000 Oct 1;165(7):3680-8. doi: 10.4049/jimmunol.165.7.3680.
Humans and mice with genetic deficiencies that lead to loss of signaling through common gamma-chain (gammac)-containing cytokine receptors have severe defects in B and T lymphocytes. In humans, these deficiencies lead to a complete absence of T cells, whereas in mice, small thymuses give rise to normal numbers of peripheral T cells. We have examined the first wave of developing T cells in Jak3-/-, IL-7-/-, and IL-7Ralpha-/- fetal mice, and have found a near absence of thymic progenitor cells. This deficiency is highlighted by the complete inability of Jak3-/- progenitor cells to reconstitute T cell development in the presence of competing wild-type cells. These data clearly demonstrate a strong common basis for the T cell deficiencies in mice and humans lacking gammac/Jak3 signaling pathways.
由于基因缺陷导致通过含共同γ链(γc)的细胞因子受体信号传导缺失的人类和小鼠,其B淋巴细胞和T淋巴细胞存在严重缺陷。在人类中,这些缺陷导致T细胞完全缺失,而在小鼠中,小胸腺可产生正常数量的外周T细胞。我们检查了Jak3基因敲除、IL-7基因敲除和IL-7Rα基因敲除的胎鼠中发育中的T细胞的第一波,发现胸腺祖细胞几乎缺失。Jak3基因敲除的祖细胞在存在竞争性野生型细胞的情况下完全无法重建T细胞发育,这突出了这种缺陷。这些数据清楚地证明了缺乏γc/Jak3信号通路的小鼠和人类T细胞缺陷存在强大的共同基础。