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正常大鼠肾成纤维细胞中依赖于生长的电容性钙内流的调节。

Growth-dependent modulation of capacitative calcium entry in normal rat kidney fibroblasts.

机构信息

Department of Cell Biology, Radboud University Nijmegen, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands.

出版信息

Cell Signal. 2010 Jul;22(7):1044-53. doi: 10.1016/j.cellsig.2010.02.007. Epub 2010 Feb 24.

Abstract

Normal rat kidney (NRK) fibroblasts have electrophysiological properties and intracellular calcium dynamics that are dependent upon their growth stage. In the present study we show that this differential behavior coincides with a differential calcium entry that can be either capacitative or non-capacitative. Confluent cells made quiescent by serum deprivation, which have a stable membrane potential near -70 mV and do not show spontaneous intracellular calcium oscillations, primarily exhibit the capacitative mechanism for calcium entry, also called store-operated calcium entry (SOCE). When the quiescent cells are grown to density-arrest in the presence of EGF as the sole polypeptide growth factor, these cells characteristically fire spontaneously repetitive calcium action potentials, which propagate throughout the whole monolayer and are accompanied by intracellular calcium transients. These density-arrested cells appear to exhibit in addition to SOCE also receptor-operated calcium entry (ROCE) as a mechanism for calcium entry. Furthermore we show that, in contrast to earlier studies, the employed SOCs and ROCs are permeable for both calcium and strontium ions. We examined the expression of the canonical transient receptor potential channels (Trpcs) that may be involved in SOCE and ROCE. We show that NRK fibroblasts express the genes encoding Trpc1, Trpc5 and Trpc6, and that the levels of their expression are dependent upon the growth stage of the cells. In addition we examined the growth stage dependent expression of the genes encoding Orai1 and Stim1, two proteins that have recently been shown to be involved in SOCE. Our results suggest that the differential expression of Trpc5, Trpc6, Orai1 and Stim1 in quiescent and density-arrested NRK fibroblasts is responsible for the difference in regulation of calcium entry between these cells. Finally, we show that inhibition or potentiation of SOCE and ROCE by pharmacological agents has profound effects on calcium dynamics in NRK fibroblasts.

摘要

正常大鼠肾 (NRK) 成纤维细胞具有依赖于其生长阶段的电生理特性和细胞内钙离子动力学。在本研究中,我们表明这种差异行为与可电容或非电容的差异钙内流一致。通过血清剥夺使汇合细胞静止,其膜电位稳定在 -70 mV 附近,并且不显示自发的细胞内钙离子振荡,主要表现出钙内流的电容机制,也称为储存操作钙内流(SOCE)。当静息细胞在 EGF 存在下生长至密度停滞时,这些细胞特征性地自发重复钙动作电位,其在整个单层中传播,并伴有细胞内钙瞬变。这些密度停滞的细胞似乎除了 SOCE 之外还表现出受体操作钙内流(ROCE)作为钙内流的机制。此外,我们表明,与早期研究相反,所采用的 SOC 和 ROC 对钙和锶离子都具有通透性。我们检查了可能参与 SOCE 和 ROCE 的经典瞬时受体电位通道(Trpcs)的表达。我们表明,NRK 成纤维细胞表达编码 Trpc1、Trpc5 和 Trpc6 的基因,并且它们的表达水平取决于细胞的生长阶段。此外,我们检查了基因编码 Orai1 和 Stim1 的生长阶段依赖性表达,这两种蛋白质最近被证明参与 SOCE。我们的结果表明,Trpc5、Trpc6、Orai1 和 Stim1 在静止和密度停滞的 NRK 成纤维细胞中的差异表达是这些细胞之间钙内流调节差异的原因。最后,我们表明,药理学试剂对 SOCE 和 ROCE 的抑制或增强对 NRK 成纤维细胞钙动力学有深远影响。

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