Reeves W G, Zamkoff K W, Poiesz B J, Paolozzi F P, Tomar R H, Moore J L, Ruscetti F W
J Biol Response Mod. 1985 Feb;4(1):83-95.
Proliferation of normal human T cells in vitro requires activation of resting T cells by lectin or antigen. This stimulation initiates a series of events which includes elaboration of T cell growth factor (TCGF), expression of TCGF receptors, and, ultimately, cellular proliferation. We sought to determine if TCGF was required for expression of the TCGF receptor in phytohemagglutinin (PHA)-stimulated normal human T cells. Utilizing dexamethasone (DEX), a known inhibitor of TCGF production, reductions in T cell proliferation, TCGF production, and TCGF receptor expression, as measured by TCGF adsorption and Tac acquisition, were demonstrated after PHA stimulation. When exogenous partially purified TCGF was added to DEX-containing cultures, the DEX inhibition of proliferation and TCGF receptor expression was completely reversed. These experiments were reproduced utilizing both highly purified TCGF from the Jurkat cell line and purified TCGF synthesized by bacteria from cloned TCGF DNA. Short-term experiments showed TCGF to be capable of restoring Tac antigen expression after DEX inhibition in the absence of cellular proliferation. These results indicate that TCGF is required for optimal expression of Tac antigen-associated TCGF receptors in PHA-activated T cells.
正常人T细胞在体外增殖需要凝集素或抗原激活静止T细胞。这种刺激引发一系列事件,包括T细胞生长因子(TCGF)的产生、TCGF受体的表达,以及最终的细胞增殖。我们试图确定在植物血凝素(PHA)刺激的正常人T细胞中,表达TCGF受体是否需要TCGF。使用地塞米松(DEX),一种已知的TCGF产生抑制剂,在PHA刺激后,通过TCGF吸附和Tac获得量测量,T细胞增殖、TCGF产生和TCGF受体表达均降低。当将外源性部分纯化的TCGF添加到含DEX的培养物中时,DEX对增殖和TCGF受体表达的抑制作用完全逆转。利用来自Jurkat细胞系的高度纯化的TCGF和由细菌从克隆的TCGF DNA合成的纯化TCGF重复了这些实验。短期实验表明,在无细胞增殖的情况下,DEX抑制后TCGF能够恢复Tac抗原表达。这些结果表明,在PHA激活的T细胞中,TCGF是Tac抗原相关的TCGF受体最佳表达所必需的。