Gauchat J F, Khandjian E W, Weil R
Proc Natl Acad Sci U S A. 1986 Sep;83(17):6430-4. doi: 10.1073/pnas.83.17.6430.
Blast formation and mitotic activation of G0-arrested mouse thymocytes were triggered by the addition of concanavalin A plus interleukin 2 (IL-2) to the culture medium. When added alone, Con A induces within 6 hr a complex reprogramming ("priming") that comprises the activation of the IL-2 receptor gene. The primed thymocytes are competent to interact with IL-2 and to respond to its growth-promoting effect, which corresponds to blast formation and mitotic activation. Cyclosporin A, an immunosuppressive cyclic peptide of fungal origin, prevents in T lymphocytes the activation of a set(s) of genes encoding lymphokines and the IL-2 receptor but does not affect their expression once they have been activated. The biomedical implications of these observations are discussed.
通过向培养基中添加伴刀豆球蛋白A(Con A)和白细胞介素2(IL-2),可触发处于G0期停滞的小鼠胸腺细胞的母细胞形成和有丝分裂激活。单独添加Con A时,在6小时内可诱导一种复杂的重编程(“致敏”),其中包括IL-2受体基因的激活。致敏的胸腺细胞能够与IL-2相互作用并对其促生长作用作出反应,这与母细胞形成和有丝分裂激活相对应。环孢菌素A是一种源自真菌的免疫抑制性环肽,可在T淋巴细胞中阻止一组编码淋巴因子和IL-2受体的基因的激活,但一旦这些基因被激活,环孢菌素A不会影响它们的表达。本文讨论了这些观察结果的生物医学意义。