胸腺激素、Ca2+和chalone-T对T淋巴细胞分化和增殖的调控。

I Blazsek
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摘要

在C57Bl/6小鼠中研究了胸腺分化因子胸腺激素家族(thymosin fr. 5, A. L. Goldstein)、Ca2+和纯化抑制蛋白对T淋巴细胞增殖的调节作用。1.2 mM Ca2+浓度对小鼠胸腺细胞生长最有利。浓度大于2 mM的Cu2+可暂时抑制净蛋白的合成,这种抑制作用在2小时后对DNA合成产生明显抑制。5 .胸腺素的作用轻微,持续时间短,性质振荡;相比之下,chalone-T制剂可永久抑制胸腺细胞DNA合成长达12小时的培养。用免疫佐剂卡介苗(BCG)处理的小鼠脾脏细胞暴露于培养物中的chalone-T,然后用PHA刺激,与对照或正常未激活BCG的小鼠脾脏细胞相比,经chalone-T预处理的培养物中增殖反应降低。这一结果提示,chalone-T对胸腺细胞具有双重作用,即抑制细胞周期进程和诱导抑制性T淋巴细胞表型转化。讨论了T淋巴细胞产生的多因子概念。
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Regulation of T lymphocyte differentiation and proliferation by thymus hormones, Ca2+ and chalone-T.

The regulatory effect on T lymphocyte proliferation of the differentiator thymosin hormone family (thymosin fr. 5, A. L. Goldstein), Ca2+, and purified inhibitory protein fractions prepared from calf thymus was investigated in C57Bl/6 mice. 1.2 mM Ca2+ concentration was the most favourable for murine thymocyte growth in culture. Net protein synthesis was transitorily inhibited by Cu2+ concentrations higher than 2 mM. This inhibition was followed by a marked inhibition of DNA synthesis 2 hrs later. The effect of thymosin fr. 5 was slight, of short duration, and oscillatory in nature; in contrast, chalone-T preparations inhibited thymocyte DNA synthesis permanently up to 12 hrs of cultivation. When spleen cells taken from mice treated with the immunoadjuvant Bacillus Calmette-Guérin (BCG) were exposed to chalone-T in culture, then stimulated with PHA, a reduced proliferative response was measured in chalone-T pretreated cultures compared to controls or spleen cells from normal non-BCG-activated mice. This result had led us to suggest that chalone-T has a dual effect on thymocytes, viz. it inhibits cell cycle progression and induces the phenotypic conversion of suppressor T lymphocytes. The multifactorial concept of T lymphocyte production is discussed.

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