首页> 外文期刊>Developmental biology >NT-3 and CNTF exert dose-dependent, pleiotropic effects on cells in the immature dorsal root ganglion: neuregulin-mediated proliferation of progenitor cells and neuronal differentiation.
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NT-3 and CNTF exert dose-dependent, pleiotropic effects on cells in the immature dorsal root ganglion: neuregulin-mediated proliferation of progenitor cells and neuronal differentiation.

机译:NT-3和CNTF对未成熟的背根神经节中的细胞发挥剂量依赖性,多效性作用:神经调节蛋白介导的祖细胞增殖和神经元分化。

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摘要

Neurons in the nascent dorsal root ganglia are born and differentiate in a complex cellular milieu composed of postmitotic neurons, and mitotically active glial and neural progenitor cells. Neurotrophic factors such as NT-3 are critically important for promoting the survival of postmitotic neurons in the DRG. However, the factors that regulate earlier events in the development of the DRG such as the mitogenesis of DRG progenitor cells and the differentiation of neurons are less defined. Here we demonstrate that both NT-3 and CNTF induce distinct dose-dependent responses on cells in the immature DRG: at low concentrations, they induce the proliferation of progenitor cells while at higher concentrations they promote neuronal differentiation. Furthermore, the mitogenic response is indirect; that is, NT-3 and CNTF first bind to nascent neurons in the DRG--which then stimulates those neurons to release mitogenic factors including neuregulin. Blockade of this endogenous neuregulin activity completely blocks the CNTF-induced proliferation and reduces about half of the NT-3-mediated proliferation. Thus, the genesis and differentiation of neurons and glia in the DRG are dependent upon reciprocal interactions among nascent neurons, glia, and mitotically active progenitor cells.
机译:新生背根神经节中的神经元在由有丝分裂后神经元以及有丝分裂活跃的神经胶质和神经祖细胞组成的复杂细胞环境中出生并分化。 NT-3等神经营养因子对于促进DRG中有丝分裂后神经元的存活至关重要。然而,调节DRG发育早期事件的因素,例如DRG祖细胞的有丝分裂和神经元的分化,尚不清楚。在这里,我们证明NT-3和CNTF对未成熟DRG中的细胞诱导不同的剂量依赖性反应:低浓度时,它们诱导祖细胞增殖,而高浓度时,它们促进神经元分化。此外,有丝分裂反应是间接的。也就是说,NT-3和CNTF首先与DRG中新生的神经元结合,然后刺激这些神经元释放有丝分裂因子,包括神经调节蛋白。内源性神经调节蛋白活性的阻断完全阻断了CNTF诱导的增殖,并减少了NT-3介导的增殖的一半。因此,DRG中神经元和神经胶质的发生和分化取决于新生神经元,神经胶质和有丝分裂活性祖细胞之间的相互相互作用。

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