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环磷酸腺苷对S49淋巴瘤细胞生长的调控

Regulation of S49 lymphoma cell growth by cyclic adenosine 3':5'-monophosphate.

作者信息

Coffino P, Gray J W

出版信息

Cancer Res. 1978 Nov;38(11 Pt 2):4285-8.

PMID:212191
Abstract

S49 lymphoma tissue culture cells arrest in the G1 phase of the cell cycle when treated with agents that elevate endogenous cyclic adenosine 3':5'-monophosphate (cAMP), such as cholera toxin or exogenously added active congeners of cAMP such as N6,O2'-dibutyryl cyclic adenosine 3':5'-monophosphate (Bt2cAMP). This phenomenon requires that cells contain the appropriate receptors: Mutant cells deficient in adenylyl cyclase fail to arrest in response to cholera toxin, and another mutant that lacks cAMP-dependent protein kinase does not respond to cholera toxin or to Bt2cAMP. The size distribution of cell populations treated with Bt2cAMP changes in a manner that reflects only the perturbation of cell cycle distribution. Arrested G1 cells in particular have the same volume as the G1 cells of an exponentially growing population. When G1 cells that have been arrested by Bt2cAMP are grown in fresh medium free of Bt2cAMP, they begin to reenter S phase after a delay of about 6 hr and do so with pseudo-first-order kinetics, with a half-life of 5 hr. These and other properties previously described suggest that cAMP regulates S49 cell growth by physiologically significant rather than artifactual mechanisms.

摘要

当用能提高内源性环磷酸腺苷(cAMP)的试剂处理时,S49淋巴瘤组织培养细胞会停滞在细胞周期的G1期,这些试剂如霍乱毒素,或外源性添加的cAMP活性类似物,如N6,O2'-二丁酰环磷酸腺苷(Bt2cAMP)。这种现象要求细胞含有适当的受体:腺苷酸环化酶缺陷的突变细胞对霍乱毒素无反应而不会停滞,另一种缺乏cAMP依赖性蛋白激酶的突变体对霍乱毒素或Bt2cAMP也无反应。用Bt2cAMP处理的细胞群体的大小分布变化方式仅反映细胞周期分布的扰动。特别是停滞的G1期细胞与指数生长群体中的G1期细胞具有相同的体积。当被Bt2cAMP停滞的G1期细胞在不含Bt2cAMP的新鲜培养基中生长时,它们在延迟约6小时后开始重新进入S期,并以准一级动力学进行,半衰期为5小时。先前描述的这些及其他特性表明,cAMP通过生理上有意义而非人为的机制调节S49细胞生长。

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