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人诱导多能干细胞源性神经发生过程中钙激活钾通道的表达。

Calcium activated potassium channel expression during human iPS cell-derived neurogenesis.

机构信息

Institute for Anatomy & Cell Biology, Ulm University, Ulm, Germany.

Department of Internal Medicine I, Ulm University, Ulm, Germany.

出版信息

Ann Anat. 2013 Jul;195(4):303-311. doi: 10.1016/j.aanat.2013.02.009. Epub 2013 Mar 28.

Abstract

The family of calcium activated potassium channels of low and intermediate conductance, known as SK channels, consists of four members (SK1-4). These channels are widely expressed throughout the organism and involved in various cellular processes, such as the afterhyperpolarization in excitable cells but also in differentiation processes of various tissues. To date, the role of SK channels in developmental processes has been merely a marginal focus of investigation, although it is well accepted that cell differentiation and maturation affect the expression patterns of certain ion channels. Recently, several studies from our laboratory delineated the influence of SK channel expression and their respective activity on cytoskeletal reorganization in neural and pluripotent stem cells and regulation of cell fate determination toward the cardiac lineage in human and mouse pluripotent stem cells. Herein, we have now analyzed SK channel expression patterns and distribution at various stages of human induced pluripotent stem cell-derived neurogenesis particularly focusing on undifferentiated iPS cells, neural progenitors and mature neurons. All family members could be detected starting at the iPS cell level and were differentially expressed during the subsequent maturation process. Intriguingly, we found obvious discrepancies between mRNA and protein expression pointing toward a complex regulatory mechanism. Inhibition of SK channels with either apamin or clotrimazol did not have any significant effects on the speed or amount of neurogenesis in vitro. The abundance and specific regulation of SK channel expression during iPS cell differentiation indicates distinct roles of these ion channels not only for the cardiac but also for neuronal cell differentiation and in vitro neurogenesis.

摘要

钙激活的钾通道家族中的低和中等电导通道,称为 SK 通道,由四个成员(SK1-4)组成。这些通道在整个生物体中广泛表达,参与各种细胞过程,例如兴奋细胞的后超极化,但也参与各种组织的分化过程。迄今为止,SK 通道在发育过程中的作用仅仅是研究的一个次要焦点,尽管人们普遍认为细胞分化和成熟会影响某些离子通道的表达模式。最近,我们实验室的几项研究描述了 SK 通道表达及其各自活性对神经和多能干细胞中细胞骨架重排的影响,以及对人源和鼠源多能干细胞向心脏谱系的细胞命运决定的调节。在此,我们现在分析了 SK 通道在人诱导多能干细胞衍生神经发生的各个阶段的表达模式和分布,特别是在未分化的 iPS 细胞、神经祖细胞和成熟神经元中。从 iPS 细胞水平开始就可以检测到所有家族成员,并且在随后的成熟过程中表现出不同的表达。有趣的是,我们发现 mRNA 和蛋白质表达之间存在明显差异,表明存在复杂的调节机制。用 apamin 或 clotrimazol 抑制 SK 通道对体外神经发生的速度或数量没有任何显著影响。在 iPS 细胞分化过程中,SK 通道的表达丰度和特异性调节表明这些离子通道不仅在心脏,而且在神经元细胞分化和体外神经发生中具有独特的作用。

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