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轴突衍生的神经调节蛋白促进发育中大鼠视神经少突胶质细胞存活的证据。

Evidence that axon-derived neuregulin promotes oligodendrocyte survival in the developing rat optic nerve.

作者信息

Fernandez P A, Tang D G, Cheng L, Prochiantz A, Mudge A W, Raff M C

机构信息

Department of Biology, University College London, United Kingdom.

出版信息

Neuron. 2000 Oct;28(1):81-90. doi: 10.1016/s0896-6273(00)00087-8.

Abstract

It was previously shown that newly formed oligodendrocytes depend on axons for their survival, but the nature of the axon-derived survival signal(s) remained unknown. We show here that neuregulin (NRG) supports the survival of purified oligodendrocytes and aged oligodendrocyte precursor cells (OPCs) but not of young OPCs. We demonstrate that axons promote the survival of purified oligodendrocytes and that this effect is inhibited if NRG is neutralized. In the developing rat optic nerve, we provide evidence that delivery of NRG decreases both normal oligodendrocyte death and the extra oligodendrocyte death induced by nerve transection, whereas neutralization of endogenous NRG increases the normal death. These results suggest that NRG is an axon-associated survival signal for developing oligodendrocytes.

摘要

先前的研究表明,新形成的少突胶质细胞的存活依赖于轴突,但其轴突衍生的存活信号的性质仍不清楚。我们在此表明,神经调节蛋白(NRG)支持纯化的少突胶质细胞和衰老的少突胶质前体细胞(OPC)的存活,但不支持年轻OPC的存活。我们证明轴突促进纯化的少突胶质细胞的存活,并且如果NRG被中和,这种作用就会受到抑制。在发育中的大鼠视神经中,我们提供证据表明,给予NRG可减少正常少突胶质细胞死亡以及神经横断诱导的额外少突胶质细胞死亡,而内源性NRG的中和则会增加正常死亡。这些结果表明,NRG是发育中的少突胶质细胞的一种轴突相关存活信号。

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