Cell cycle-dependent regulation of cellular ATP concentration, and depolymerization of the interphase microtubular network induced by elevated cellular ATP concentration in whole fibroblasts.

M Marcussen, P J Larsen
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引用次数: 43

Abstract

In the present work, evidence is presented indicating that an increased cellular ATP concentration during mitosis may, in conjunction with other factors [Verde et al., 1990: Nature 343:233-238; Andersen et al., 1994: J Cell Biol. 127:1289-1299], induce depolymerization of the interphase microtubular network in cultured fibroblasts. It is shown here that the cellular ATP concentration varies through the cell cycle, reaching a peak at G2M- and minimum at late G1/early S-phase. Furthermore, we have found, using indirect immunofluorescent staining with an antitubulin antibody, that depolymerization of the interphase microtubular network may be induced by increasing the intracellular ATP concentration in cultured fibroblasts from 2.2 mM to 4.1 mM. This may be obtained through addition of adenosine and P1 to the growth medium. Our results indicate that this effect of adenosine and Pi is not mediated via adenosine receptors, but through an elevated cellular ATP concentration. ATP is suggested to act through a concentration-dependent effect on the exchangeable GTP site on tubulin, and not through the action of protein kinases or microtubule-associated proteins.

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细胞周期依赖性的细胞ATP浓度调控,以及全成纤维细胞ATP浓度升高诱导的间期微管网络解聚。
在目前的工作中,有证据表明有丝分裂期间细胞ATP浓度的增加可能与其他因素一起[Verde等人,1990:Nature 343:233-238;[J] .中国生物医学工程学报,2010,27 (1):1 - 2 .]结果表明,细胞ATP浓度随细胞周期的变化而变化,在G2M期达到峰值,在G1晚期/ s期早期达到最低。此外,我们发现,使用抗微管蛋白抗体的间接免疫荧光染色,可以通过将培养成纤维细胞的细胞内ATP浓度从2.2 mM增加到4.1 mM来诱导间期微管网络的解聚。这可以通过在生长培养基中添加腺苷和P1来实现。我们的研究结果表明,腺苷和Pi的这种作用不是通过腺苷受体介导的,而是通过升高的细胞ATP浓度介导的。提示ATP通过浓度依赖性作用于微管蛋白上的可交换GTP位点,而不是通过蛋白激酶或微管相关蛋白的作用。
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