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PDGF and FGF-2 signaling in oligodendrocyte progenitor cells: regulation of proliferation and differentiation by multiple intracellular signaling pathways.

机译:少突胶质祖细胞中的PDGF和FGF-2信号转导:通过多种细胞内信号转导途径调节增殖和分化。

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摘要

In this paper we address the linking of platelet-derived growth factor (PDGF) and basic fibroblast growth factor (FGF-2) to intracellular signaling molecules in oligodendrocyte progenitors. It is demonstrated that both growth factors activate downstream targets similar to those shown for protein kinase C (PKC) activation. Yet, neither the arrest of terminal oligodendrocyte differentiation nor the proliferation induced by PDGF or FGF-2 can be antagonized by inhibition of PKC. Rather, p42/p44 mitogen-activated protein kinase (MAPK), p38 MAPK, and pp70 S6 kinase were found to be necessary for the mitogenic activity of PDGF and FGF-2. Paradoxically, these kinases were also necessary for the onset of oligodendrocyte differentiation in control cells. In addition, cAMP-dependent kinase A (PKA) activation inhibited the mitogenic response of oligodendrocyte progenitors to FGF-2. Taken together, the molecular mechanism that controls oligodendrocyte lineage progression is operated by at least two signal pathways, which interfere either with proliferation and/or differentiation of oligodendrocyte progenitors. Copyright 2000 Academic Press.
机译:在本文中,我们探讨了血小板衍生生长因子(PDGF)和碱性成纤维细胞生长因子(FGF-2)与少突胶质祖细胞中细胞内信号分子的联系。已证明这两种生长因子均激活下游靶标,类似于蛋白激酶C(PKC)激活所显示的靶标。然而,终末少突胶质细胞分化的停止或PDGF或FGF-2诱导的增殖都不能通过抑制PKC来拮抗。相反,发现p42 / p44丝裂原活化蛋白激酶(MAPK),p38 MAPK和pp70 S6激酶对于PDGF和FGF-2的促有丝分裂活性是必需的。矛盾的是,这些激酶对于控制细胞中少突胶质细胞分化的发生也是必需的。此外,cAMP依赖性激酶A(PKA)激活抑制少突胶质细胞祖细胞对FGF-2的促有丝分裂反应。综上所述,控制少突胶质细胞谱系发展的分子机制是通过至少两个信号通路来进行的,这些信号通路干扰少突胶质细胞祖细胞的增殖和/或分化。版权所有2000学术出版社。

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