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一种逆行性神经元存活反应:靶源性神经营养因子调节MEF2D和bcl-w。

A retrograde neuronal survival response: target-derived neurotrophins regulate MEF2D and bcl-w.

作者信息

Pazyra-Murphy Maria F, Hans Aymeric, Courchesne Stephanie L, Karch Christoph, Cosker Katharina E, Heerssen Heather M, Watson Fiona L, Kim Taekyung, Greenberg Michael E, Segal Rosalind A

机构信息

Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Neurosci. 2009 May 20;29(20):6700-9. doi: 10.1523/JNEUROSCI.0233-09.2009.

Abstract

Survival and maturation of dorsal root ganglia sensory neurons during development depend on target-derived neurotrophins. These target-derived signals must be transmitted across long distances to alter gene expression. Here, we address the possibility that long-range retrograde signals initiated by target-derived neurotrophins activate a specialized transcriptional program. The transcription factor MEF2D is expressed in sensory neurons; we show that expression of this factor is induced in response to target-derived neurotrophins that stimulate the distal axons. We demonstrate that MEF2D regulates expression of an anti-apoptotic bcl-2 family member, bcl-w. Expression of mef2d and bcl-w is stimulated in response to activation of a Trk-dependent ERK5/MEF2 pathway, and our data indicate that this pathway promotes sensory neuron survival. We find that mef2d and bcl-w are members of a larger set of retrograde response genes, which are preferentially induced by neurotrophin stimulation of distal axons. Thus, activation of an ERK5/MEF2D transcriptional program establishes and maintains the cellular constituents of functional sensory circuits.

摘要

背根神经节感觉神经元在发育过程中的存活和成熟依赖于靶源性神经营养因子。这些靶源性信号必须远距离传递以改变基因表达。在此,我们探讨由靶源性神经营养因子引发的长距离逆行信号激活特定转录程序的可能性。转录因子MEF2D在感觉神经元中表达;我们发现该因子的表达是对刺激远端轴突的靶源性神经营养因子的应答诱导产生的。我们证明MEF2D调节抗凋亡bcl-2家族成员bcl-w的表达。响应Trk依赖的ERK5/MEF2途径的激活,mef2d和bcl-w的表达受到刺激,并且我们的数据表明该途径促进感觉神经元存活。我们发现mef2d和bcl-w是一组更大的逆行反应基因的成员,这些基因优先由神经营养因子对远端轴突的刺激诱导产生。因此,ERK5/MEF2D转录程序的激活建立并维持了功能性感觉回路的细胞成分。

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