Chittajallu R, Chen Y, Wang H, Yuan X, Ghiani C A, Heckman T, McBain C J, Gallo V
Laboratory of Cellular and Synaptic Neurophysiology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-4495, USA.
Proc Natl Acad Sci U S A. 2002 Feb 19;99(4):2350-5. doi: 10.1073/pnas.042698399.
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.
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。