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来自纯培养和混合培养的皮质神经元的钙离子通道电流

Ca(2+) channel currents of cortical neurons from pure and mixed cultures.

作者信息

Zhou Chen, Yang Aiying, Chai Zhen

机构信息

State Key Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing, 100871, China.

出版信息

Cytotechnology. 2012 Mar;64(2):173-9. doi: 10.1007/s10616-011-9405-2. Epub 2011 Dec 6.

DOI:10.1007/s10616-011-9405-2
PMID:22143344
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3279576/
Abstract

Voltage-gated Ca(2+) channels (VGCCs) are key regulators of many neuronal functions, and involved in multiple central nervous system diseases. In the last 30 years, a large number of injury and disease models have been established based on cultured neurons. Culture with serum develops a mixture of neurons and glial cells, while culture without serum develops pure neurons. Both of these neuronal-culture methods are widely used. However, the properties of Ca(2+) currents in neurons from these two cultures have not been compared. In this study, we cultured rat cortical neurons in serum-containing or -free medium and then recorded the Ca(2+) channel currents using patch-clamp technique. Our results showed that there were significant differences in the amplitude and activation properties of whole-cell Ca(2+) channel currents, and of non-L-type Ca(2+) channel currents between the neurons from these two culture systems. Our data suggested that the difference of whole-cell Ca(2+) currents may result from the differences in non-L-type currents. Understanding of these properties will considerably advance studies of VGCCs in neurons from pure or mixed culture.

摘要

电压门控性钙通道(VGCCs)是多种神经元功能的关键调节因子,并参与多种中枢神经系统疾病。在过去30年里,基于培养的神经元建立了大量损伤和疾病模型。含血清培养会产生神经元和神经胶质细胞的混合物,而无血清培养则产生纯神经元。这两种神经元培养方法都被广泛使用。然而,尚未对这两种培养物中神经元的钙电流特性进行比较。在本研究中,我们将大鼠皮质神经元培养于含血清或无血清培养基中,然后使用膜片钳技术记录钙通道电流。我们的结果表明,这两种培养系统来源的神经元之间,全细胞钙通道电流以及非L型钙通道电流的幅度和激活特性存在显著差异。我们的数据表明,全细胞钙电流的差异可能源于非L型电流的差异。了解这些特性将极大地推动对纯培养或混合培养神经元中VGCCs的研究。

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本文引用的文献

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Brain Res. 2009 Jun 18;1276:159-70. doi: 10.1016/j.brainres.2009.04.022. Epub 2009 Apr 21.
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