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延迟整流钾通道和A 型钾通道与胚胎大鼠神经祖细胞中Kv 2.1和Kv 4.3的表达相关。

Delayed rectifier and A-type potassium channels associated with Kv 2.1 and Kv 4.3 expression in embryonic rat neural progenitor cells.

作者信息

Smith Dean O, Rosenheimer Julie L, Kalil Ronald E

机构信息

Stem Cell Research Laboratory, University of Hawaii at Manoa, Manoa, Hawaii, USA.

出版信息

PLoS One. 2008 Feb 13;3(2):e1604. doi: 10.1371/journal.pone.0001604.

Abstract

BACKGROUND

Because of the importance of voltage-activated K(+) channels during embryonic development and in cell proliferation, we present here the first description of these channels in E15 rat embryonic neural progenitor cells derived from the subventricular zone (SVZ). Activation, inactivation, and single-channel conductance properties of recorded progenitor cells were compared with those obtained by others when these Kv gene products were expressed in oocytes.

METHODOLOGY/PRINCIPAL FINDINGS: Neural progenitor cells derived from the subventricular zone of E15 embryonic rats were cultured under conditions that did not promote differentiation. Immunocytochemical and Western blot assays for nestin expression indicated that almost all of the cells available for recording expressed this intermediate filament protein, which is generally accepted as a marker for uncommitted embryonic neural progenitor cells. However, a very small numbers of the cells expressed GFAP, a marker for astrocytes, O4, a marker for immature oligodendrocytes, and betaIII-tubulin, a marker for neurons. Using immunocytochemistry and Western blots, we detected consistently the expression of Kv2.1, and 4.3. In whole-cell mode, we recorded two outward currents, a delayed rectifier and an A-type current.

CONCLUSIONS/SIGNIFICANCE: We conclude that Kv2.1, and 4.3 are expressed in E15 SVZ neural progenitor cells, and we propose that they may be associated with the delayed-rectifier and the A-type currents, respectively, that we recorded. These results demonstrate the early expression of delayed rectifier and A-type K(+) currents and channels in embryonic neural progenitor cells prior to the differentiation of these cells.

摘要

背景

由于电压门控钾离子通道在胚胎发育和细胞增殖过程中具有重要作用,我们在此首次描述了源自脑室下区(SVZ)的E15大鼠胚胎神经祖细胞中的这些通道。将记录的祖细胞的激活、失活和单通道电导特性与其他研究人员在卵母细胞中表达这些Kv基因产物时获得的特性进行了比较。

方法/主要发现:将源自E15胚胎大鼠脑室下区的神经祖细胞在不促进分化的条件下培养。巢蛋白表达的免疫细胞化学和蛋白质印迹分析表明,几乎所有可用于记录的细胞都表达这种中间丝蛋白,该蛋白通常被认为是未分化胚胎神经祖细胞的标志物。然而,极少量的细胞表达了星形胶质细胞标志物GFAP、未成熟少突胶质细胞标志物O4和神经元标志物βIII-微管蛋白。通过免疫细胞化学和蛋白质印迹,我们始终检测到Kv2.1和4.3的表达。在全细胞模式下,我们记录到两种外向电流,一种延迟整流电流和一种A型电流。

结论/意义:我们得出结论,Kv2.1和4.3在E15 SVZ神经祖细胞中表达,并且我们提出它们可能分别与我们记录的延迟整流电流和A型电流相关。这些结果证明了延迟整流电流和A型钾离子电流及通道在胚胎神经祖细胞分化之前的早期表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b915/2225502/a6da9cf72041/pone.0001604.g001.jpg

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