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Mol Cell Neurosci. 2013 Sep;56:50-64. doi: 10.1016/j.mcn.2013.02.005. Epub 2013 Feb 28.
2
Genetically-modified human pluripotent stem cells: new hopes for the understanding and the treatment of neurological diseases?基因修饰的人类多能干细胞:理解和治疗神经疾病的新希望?
Curr Gene Ther. 2013 Apr;13(2):111-9. doi: 10.2174/1566523211313020005.
3
Targeting TRPs in neurodegenerative disorders.靶向神经退行性疾病中的 TRP 通道。
Curr Top Med Chem. 2013;13(3):322-34. doi: 10.2174/1568026611313030009.
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Possible involvement of TRP channels in cardiac hypertrophy and arrhythmia.TRP 通道在心肌肥厚和心律失常中的可能作用。
Curr Top Med Chem. 2013;13(3):283-94. doi: 10.2174/1568026611313030006.
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Steps toward safe cell therapy using induced pluripotent stem cells.利用诱导多能干细胞实现安全细胞疗法的步骤。
Circ Res. 2013 Feb 1;112(3):523-33. doi: 10.1161/CIRCRESAHA.111.256149.
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Identification of large families in early repolarization syndrome.早期复极综合征中大家族的鉴定。
J Am Coll Cardiol. 2013 Jan 15;61(2):164-72. doi: 10.1016/j.jacc.2012.09.040.
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The nicotinic acetylcholine receptor: the founding father of the pentameric ligand-gated ion channel superfamily.烟碱型乙酰胆碱受体:五聚体配体门控离子通道超家族的奠基人。
J Biol Chem. 2012 Nov 23;287(48):40207-15. doi: 10.1074/jbc.R112.407668. Epub 2012 Oct 4.
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Nicotinic receptors and functional regulation of GABA cell microcircuitry in bipolar disorder and schizophrenia.烟碱受体与双相情感障碍和精神分裂症中GABA能细胞微环路的功能调节
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Regulation of insulin secretion in human pancreatic islets.人胰腺胰岛中胰岛素分泌的调节。
Annu Rev Physiol. 2013;75:155-79. doi: 10.1146/annurev-physiol-030212-183754. Epub 2012 Sep 4.
10
A novel CACNA1A mutation results in episodic ataxia with migrainous features without headache.一种新型 CACNA1A 突变导致无头痛性偏头痛样发作性共济失调。
Cephalalgia. 2012 Nov;32(15):1147-9. doi: 10.1177/0333102412459572. Epub 2012 Aug 31.

基于微阵列的离子通道表达模式比较:人角质形成细胞到重编程 hiPSC 分化的神经元和心肌祖细胞。

Microarray-Based Comparisons of Ion Channel Expression Patterns: Human Keratinocytes to Reprogrammed hiPSCs to Differentiated Neuronal and Cardiac Progeny.

机构信息

Institute for Anatomy Cell Biology, Ulm University, Albert-Einstein Allee 11, 89081 Ulm, Germany.

出版信息

Stem Cells Int. 2013;2013:784629. doi: 10.1155/2013/784629. Epub 2013 Apr 15.

DOI:10.1155/2013/784629
PMID:23690787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3649712/
Abstract

Ion channels are involved in a large variety of cellular processes including stem cell differentiation. Numerous families of ion channels are present in the organism which can be distinguished by means of, for example, ion selectivity, gating mechanism, composition, or cell biological function. To characterize the distinct expression of this group of ion channels we have compared the mRNA expression levels of ion channel genes between human keratinocyte-derived induced pluripotent stem cells (hiPSCs) and their somatic cell source, keratinocytes from plucked human hair. This comparison revealed that 26% of the analyzed probes showed an upregulation of ion channels in hiPSCs while just 6% were downregulated. Additionally, iPSCs express a much higher number of ion channels compared to keratinocytes. Further, to narrow down specificity of ion channel expression in iPS cells we compared their expression patterns with differentiated progeny, namely, neurons and cardiomyocytes derived from iPS cells. To conclude, hiPSCs exhibit a very considerable and diverse ion channel expression pattern. Their detailed analysis could give an insight into their contribution to many cellular processes and even disease mechanisms.

摘要

离子通道参与多种细胞过程,包括干细胞分化。生物体中存在许多种离子通道家族,可以通过离子选择性、门控机制、组成或细胞生物学功能等来区分。为了描述这组离子通道的独特表达,我们比较了人角质形成细胞来源的诱导多能干细胞(hiPSC)与其体细胞来源的人拔毛毛囊角质细胞之间的离子通道基因的 mRNA 表达水平。这一比较显示,在 hiPSC 中,26%的分析探针显示离子通道上调,而只有 6%下调。此外,与角质细胞相比,iPSC 表达的离子通道数量要多得多。此外,为了缩小 iPS 细胞中离子通道表达的特异性,我们将其表达模式与分化后代(即源自 iPSC 的神经元和心肌细胞)进行了比较。总之,hiPSC 表现出非常丰富多样的离子通道表达模式。对其进行详细分析可以深入了解它们在许多细胞过程甚至疾病机制中的作用。