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细胞分裂的调控:一个统一的假说。

Control of cell division: a unifying hypothesis.

作者信息

Berridge M J

出版信息

J Cyclic Nucleotide Res. 1975;1(5):305-20.

PMID:178693
Abstract

A constant feature of the initiation of cell division in a number of different cells is a rise in the intracellular level of calcium. The importance of cyclic nucleotides may depend on the way they interact with calcium. Cyclic AMP is apparently not an essential regulator of cell division but through its ability to modulate the intracellular level of calcium this cyclic nucleotide can exert profound effects on cell growth. In some systems (liver and salivary glands) cyclic AMP seems to augment the calcium signal whereas in others (lymphocytes and fibroblasts) it opposes calcium and can thus inhibit cell division. A rise in the level of calcium may be responsible for the parallel increase in cyclic GMP level which is usually associated with the stimulus to divide. An appealing feature of this calcium hypothesis is that it can account for the growth characteristics revealed by fibroblasts in tissue culture or embryonic cells during development. In both cases there is an initial phase of exponential growth during which I have proposed that the high level of calcium at mitosis persists into early G1 to provide the signal for the next division. In order to account for the sudden cessation of cell division at confluency, or at a specific stage during development, it is necessary to postulate that there is something different about the final mitosis which sets it apart from earlier mitoses. It is proposed that as the cells leave the last mitosis the level of calcium falls much more rapidly than it did during preceeding mitoses perhaps as a result of a more rapid rise in the level of cyclic AMP. This rapid rise in cyclic AMP level may have a dual function. Not only will it lower the level of calcium thus preventing further division, but it may also stimulate differentiation. Many of the embryonic cells which differentiate into specialized cells (lymphocytes, liver, salivary gland) retain the ability to divide if provided with appropriate stimuli. Although the nature of these stimuli vary considerably, they all seem to act by elevating the intracellular level of calcium.

摘要

许多不同细胞开始进行细胞分裂时的一个常见特征是细胞内钙水平的升高。环核苷酸的重要性可能取决于它们与钙相互作用的方式。环磷酸腺苷显然不是细胞分裂的必需调节因子,但通过其调节细胞内钙水平的能力,这种环核苷酸可对细胞生长产生深远影响。在某些系统(肝脏和唾液腺)中,环磷酸腺苷似乎会增强钙信号,而在其他系统(淋巴细胞和成纤维细胞)中,它会对抗钙,从而抑制细胞分裂。钙水平的升高可能是环磷酸鸟苷水平平行升高的原因,而环磷酸鸟苷水平升高通常与分裂刺激有关。这个钙假说的一个吸引人的特点是,它可以解释组织培养中的成纤维细胞或发育过程中的胚胎细胞所显示的生长特征。在这两种情况下,都有一个指数增长的初始阶段,在此期间,我提出有丝分裂时的高钙水平会持续到G1早期,为下一次分裂提供信号。为了解释细胞在汇合时或发育过程中的特定阶段突然停止分裂的现象,有必要假定最后一次有丝分裂存在一些与早期有丝分裂不同的地方。有人提出,当细胞离开最后一次有丝分裂时,钙水平下降的速度比之前的有丝分裂期间快得多,这可能是由于环磷酸腺苷水平上升得更快。环磷酸腺苷水平的这种快速上升可能具有双重功能。它不仅会降低钙水平,从而阻止进一步分裂,还可能刺激分化。许多分化为特化细胞(淋巴细胞、肝脏、唾液腺)的胚胎细胞,如果受到适当刺激,仍保留分裂能力。尽管这些刺激的性质差异很大,但它们似乎都通过提高细胞内钙水平来起作用。

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