首页> 外文期刊>Brain research >Heat shock protein synthesis is affected by intracellular pH: inhibition by monensin-induced alkalosis in C6 rat glioma cells.
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Heat shock protein synthesis is affected by intracellular pH: inhibition by monensin-induced alkalosis in C6 rat glioma cells.

机译:热休克蛋白的合成受细胞内pH值的影响:莫能菌素诱导的C6大鼠神经胶质瘤细胞碱中毒抑制。

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The effect of intracellular pH (pHi) on heat shock protein (HSP) synthesis was investigated in C6 rat glioma cells. pHi changes were analysed by means of fluorescence spectroscopy in a perfused monitoring system allowing continuous measurements before, during and after treatments. HSP induction was determined by means of Western blots and autoradiographs. A 20 min heat shock (HS) of 44 degrees C decreased the pHi from 7.36 to 7.05 during exposure [17] and elicited the synthesis of heat shock proteins 2-8 h later. A pHi decrease, brought about by low extracellular pH (pHe) of 4.5 and 5.0 or 5.5, induced HSP synthesis after 1 h or 3 h, respectively. During these treatments, pHi decreased to values significantly lower than that caused by HS. Three h exposure to pHe 6.2, however, was not inductive. These results indicate that the heat shock-induced pHi decrease alone is not sufficient to stimulate HSP synthesis. In order to investigate the effect of alkaline pHi on the induction of HSP by heat, pHi was increased prior to HS treatments. Preincubation of cells at pHe ranging from 6.8 to 8.0 had little effect on pHi and on HSP synthesis. A shift of pHi to more alkaline values was achieved by adding the H+/Na+ exchanger monensin at alkaline pHe. Twenty microM monensin raised the pHi and inhibited the HSP induction depending on the pHe values: as pHe was increased from pH 7.2 to 8.0 HSP synthesis was increasingly inhibited. Monensin also diminished the HS-induced drop of pHi particularly at higher pHe. The result showed that neither a lower pHi nor a drop of pHi during HS is a necessary prerequisite for the induction, whereas alkalosis inhibits the synthesis of HSP.
机译:在C6大鼠神经胶质瘤细胞中研究了细胞内pH(pHi)对热休克蛋白(HSP)合成的影响。在灌注监测系统中通过荧光光谱法分析pHi的变化,从而可以在治疗之前,期间和之后进行连续测量。通过蛋白质印迹和放射自显影确定HSP的诱导。在暴露过程中20分钟的热激(HS)在44摄氏度下将pHi从7.36降低到7.05 [17],并在2-8小时后引发了热激蛋白的合成。 pHi的降低(分别由4.5和5.0或5.5的低细胞外pH(pHe)引起)在1 h或3 h后诱导HSP合成。在这些治疗过程中,pHi降至明显低于HS引起的pHi值。然而,pHe 6.2暴露三小时不是感应的。这些结果表明,仅由热激引起的pHi降低不足以刺激HSP合成。为了研究碱性pHi对热诱导HSP的影响,在HS处理之前先增加pHi。在6.8至8.0的pHe范围内对细胞进行预孵育对pHi和HSP合成几乎没有影响。通过在碱性pHe处添加H + / Na +交换莫能菌素,可将pHi移至更大的碱性值。 20 microM莫能菌素根据pHe值升高pHi并抑制HSP诱导:随着pHe从pH 7.2增加到8.0,HSP合成受到越来越多的抑制。莫能菌素还减少了HS诱导的pHi下降,特别是在较高pHe时。结果表明,HS期间较低的pHi或pHi的下降都不是诱导的必要先决条件,而碱中毒则抑制了HSP的合成。

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