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本文引用的文献

1
Inhibition of cyclin E-cyclin-dependent kinase 2 complex formation and activity is associated with cell cycle arrest and withdrawal in oligodendrocyte progenitor cells.细胞周期蛋白E-细胞周期蛋白依赖性激酶2复合物形成及活性的抑制与少突胶质前体细胞的细胞周期停滞和退出相关。
J Neurosci. 2001 Feb 15;21(4):1274-82. doi: 10.1523/JNEUROSCI.21-04-01274.2001.
2
Modulation of Kv1.5 currents by Src tyrosine phosphorylation: potential role in the differentiation of astrocytes.Src 酪氨酸磷酸化对 Kv1.5 电流的调节:在星形胶质细胞分化中的潜在作用
J Neurosci. 2000 Jul 15;20(14):5245-53. doi: 10.1523/JNEUROSCI.20-14-05245.2000.
3
Conditional expression of RNA polymerase II in mammalian cells. Deletion of the carboxyl-terminal domain of the large subunit affects early steps in transcription.RNA聚合酶II在哺乳动物细胞中的条件性表达。大亚基羧基末端结构域的缺失影响转录的早期步骤。
J Biol Chem. 2000 Aug 11;275(32):24375-82. doi: 10.1074/jbc.M001883200.
4
Correolide and derivatives are novel immunosuppressants blocking the lymphocyte Kv1.3 potassium channels.柯瑞奥利德及其衍生物是一类新型免疫抑制剂,可阻断淋巴细胞Kv1.3钾通道。
Cell Immunol. 1999 Nov 1;197(2):99-107. doi: 10.1006/cimm.1999.1569.
5
Axonal control of oligodendrocyte development.轴突对少突胶质细胞发育的调控
J Cell Biol. 1999 Dec 13;147(6):1123-8. doi: 10.1083/jcb.147.6.1123.
6
A Kv1.5 to Kv1.3 switch in endogenous hippocampal microglia and a role in proliferation.内源性海马小胶质细胞中Kv1.5到Kv1.3的转换及其在增殖中的作用。
J Neurosci. 1999 Dec 15;19(24):10680-93. doi: 10.1523/JNEUROSCI.19-24-10680.1999.
7
Heterogeneous expression of voltage-gated potassium channels of the shaker family (Kv1) in oligodendrocyte progenitors.少突胶质前体细胞中震荡器家族电压门控钾通道(Kv1)的异质性表达。
Brain Res. 1999 Oct 2;843(1-2):145-60. doi: 10.1016/s0006-8993(99)01938-1.
8
Molecular diversity of K+ channels.钾离子通道的分子多样性
Ann N Y Acad Sci. 1999 Apr 30;868:233-85. doi: 10.1111/j.1749-6632.1999.tb11293.x.
9
Voltage-activated K+ channels and membrane depolarization regulate accumulation of the cyclin-dependent kinase inhibitors p27(Kip1) and p21(CIP1) in glial progenitor cells.电压激活的钾离子通道和膜去极化调节神经胶质祖细胞中细胞周期蛋白依赖性激酶抑制剂p27(Kip1)和p21(CIP1)的积累。
J Neurosci. 1999 Jul 1;19(13):5380-92. doi: 10.1523/JNEUROSCI.19-13-05380.1999.
10
Neurotransmitter receptor activation triggers p27(Kip1 )and p21(CIP1) accumulation and G1 cell cycle arrest in oligodendrocyte progenitors.神经递质受体激活会触发少突胶质前体细胞中p27(Kip1)和p21(CIP1)的积累以及G1期细胞周期停滞。
Development. 1999 Feb;126(5):1077-90. doi: 10.1242/dev.126.5.1077.

少突胶质前体细胞中Kv1亚基表达的调控及其在细胞周期G1/S期进程中的作用。

Regulation of Kv1 subunit expression in oligodendrocyte progenitor cells and their role in G1/S phase progression of the cell cycle.

作者信息

Chittajallu R, Chen Y, Wang H, Yuan X, Ghiani C A, Heckman T, McBain C J, Gallo V

机构信息

Laboratory of Cellular and Synaptic Neurophysiology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-4495, USA.

出版信息

Proc Natl Acad Sci U S A. 2002 Feb 19;99(4):2350-5. doi: 10.1073/pnas.042698399.

DOI:10.1073/pnas.042698399
PMID:11854528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC122368/
Abstract

Proliferative oligodendrocyte progenitor cells (OPs) express large, delayed outward-rectifying K(+) currents (I(K)), whereas nondividing immature and mature oligodendrocytes display much smaller I(K). Here, we show that up-regulation of I(K) occurs in G(1) phase of the cell cycle in purified cultured OPs and is the result of an RNA synthesis-dependent, selective increase of the K(+) channel subunit proteins Kv1.3 and Kv1.5. In oligodendrocyte cells acutely isolated from developing rat brain, a decrease of cyclin D expression is observed as these cells mature along their lineage. This is accompanied by a decrease in Kv1.3 and Kv1.5 subunit expression, suggesting a role for these subunits in the proliferative potential of OPs in situ. I(K) expressed in OPs in subventricular zone and developing white matter in acutely isolated slice preparations were selectively blocked by antagonists of Kv1.3, illustrating the functional presence of this subunit in situ. Interestingly, Kv1.3 block inhibited S-phase entry of both purified OPs in culture and in tissue slice cultures. Thus, we employ both in vitro and in situ experimental approaches to show that (i) RNA-dependent synthesis of Kv1.3 and Kv1.5 subunit proteins occurs in G(1) phase of the OP cell cycle and is responsible for the observed increase in I(K), and (ii) currents through Kv1.3-containing channels play a crucial role in G(1)/S transition of proliferating OPs.

摘要

增殖性少突胶质前体细胞(OPs)表达大的、延迟外向整流钾电流(I(K)),而非分裂的未成熟和成熟少突胶质细胞的I(K)则小得多。在此,我们表明,纯化培养的OPs中I(K)的上调发生在细胞周期的G(1)期,是钾通道亚基蛋白Kv1.3和Kv1.5的RNA合成依赖性选择性增加的结果。在从发育中的大鼠脑急性分离的少突胶质细胞中,随着这些细胞沿其谱系成熟,观察到细胞周期蛋白D表达下降。这伴随着Kv1.3和Kv1.5亚基表达的减少,表明这些亚基在原位OPs的增殖潜能中起作用。在急性分离切片标本的脑室下区和发育中的白质中的OPs中表达的I(K)被Kv1.3拮抗剂选择性阻断,说明了该亚基在原位的功能存在。有趣的是,Kv1.3阻断抑制了培养物中和组织切片培养物中纯化的OPs的S期进入。因此,我们采用体外和原位实验方法表明:(i)Kv1.3和Kv1.5亚基蛋白的RNA依赖性合成发生在OP细胞周期的G(1)期,并导致观察到的I(K)增加;(ii)通过含Kv1.3通道的电流在增殖性OPs的G(1)/S转变中起关键作用。