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神经生长因子诱导大鼠嗜铬细胞瘤PC 12细胞的神经突生长:对细胞外镁离子和钙离子的依赖性。

Nerve growth factor-induced neurite outgrowth of rat pheochromocytoma PC 12 cells: dependence on extracellular Mg2+ and Ca2+.

作者信息

Koike T

出版信息

Brain Res. 1983 Dec 19;289(1-2):293-303. doi: 10.1016/0006-8993(83)90030-6.

Abstract

Dependence of neurite outgrowth on extracellular Mg2+ and Ca2+ was studied in nerve growth factor-responsive pheochromocytoma PC 12 cells under assay conditions in which neurite formation was independent of both RNA synthesis and protein synthesis. NGF-induced neurite formation occurred maximally in the presence of extracellular Mg2+ at concentrations greater than 1.0 mM. However, extracellular Ca2+ alone did not stimulate the neurite formation, and inhibited this process at higher concentrations (greater than 10 mM). These data are consistent with the fact that NGF-mediated neurite extension occurred in assay medium containing either 1.0 mM EGTA or 0.5 mM LaCl3. Other divalent cations so far tested proved to be negative, suggesting that this phenomenon appears to be specific to Mg2+. Moreover, quantitative analysis revealed that the length and thickness of neurites formed were controlled by the presence of extracellular Ca2+. Thus, neurites formed at lower concentrations of Ca2+ in the presence of 1.0 mM Mg2+ and NGF were found to be thinner and longer than those formed at higher concentrations of Ca2+, suggesting that Ca2+ and Mg2+ have separate regulatory functions in the formation of neurites of PC 12 cells.

摘要

在神经突形成独立于RNA合成和蛋白质合成的检测条件下,研究了神经生长因子反应性嗜铬细胞瘤PC 12细胞中神经突生长对细胞外Mg2+和Ca2+的依赖性。在细胞外Mg2+浓度大于1.0 mM的情况下,NGF诱导的神经突形成最大程度地发生。然而,单独的细胞外Ca2+不会刺激神经突形成,并且在较高浓度(大于10 mM)时会抑制这一过程。这些数据与在含有1.0 mM EGTA或0.5 mM LaCl3的检测培养基中发生NGF介导的神经突延伸这一事实一致。迄今为止测试的其他二价阳离子被证明是阴性的,这表明这种现象似乎对Mg2+具有特异性。此外,定量分析表明,形成的神经突的长度和厚度受细胞外Ca2+的存在控制。因此,发现在1.0 mM Mg2+和NGF存在下,在较低Ca2+浓度下形成的神经突比在较高Ca2+浓度下形成的神经突更细更长,这表明Ca2+和Mg2+在PC 12细胞神经突形成中具有独立的调节功能。

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