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神经营养因子通过蛋白激酶C-δ依赖性机制诱导p75神经营养因子受体上调。

Neurotrophin-induced upregulation of p75NTR via a protein kinase C-delta-dependent mechanism.

作者信息

Rankin Sherri L, Guy Clifford S, Rahimtula Masuma, Mearow Karen M

机构信息

Division of BioMedical Sciences, Memorial University of Newfoundland, St. John's NL, Canada.

出版信息

Brain Res. 2008 Jun 27;1217:10-24. doi: 10.1016/j.brainres.2008.03.076. Epub 2008 Apr 9.

DOI:10.1016/j.brainres.2008.03.076
PMID:18511024
Abstract

Neurotrophins exert their biological effects via p75NTR and Trk receptors. Functional interplay between these two receptors has been widely explored with respect to p75NTR enhancing the activation and signalling of Trk, but few studies address the bidirectional aspects. We have previously demonstrated that the expression of p75NTR can be differentially modulated by different Trk receptor mutations. Here we investigate the mechanism of Nerve Growth Factor (NGF)-induced upregulation of p75NTR expression. We utilize pharmacological inhibition to investigate the role of various TrkA-associated signalling intermediates in this regulatory cascade. Notably, the inhibition of phospholipase C-gamma (PLC-gamma) using U73122, prevented the NGF-induced upregulation of p75NTR protein and mRNA. The inhibition of protein kinase C-delta (PKC-delta) activation by rottlerin, a selective PKC-delta inhibitor, and by small interfering RNA (siRNA) directed against PKC-delta also inhibited this NGF-induced upregulation. Finally, we also show that in cerebellar granule neurons, BDNF acting via TrkB increases p75NTR expression in a PKC-delta dependent manner. These results indicate the importance of Trk-dependent PLC-gamma and PKC-delta activation for downstream regulation of p75NTR protein expression in response to neurotrophin stimulation, a process that has implications to the survival and growth of the developing nervous system.

摘要

神经营养因子通过p75NTR和Trk受体发挥其生物学效应。关于p75NTR增强Trk的激活和信号传导,这两种受体之间的功能相互作用已得到广泛研究,但很少有研究涉及双向作用。我们之前已经证明,p75NTR的表达可被不同的Trk受体突变差异调节。在此,我们研究神经生长因子(NGF)诱导p75NTR表达上调的机制。我们利用药理学抑制来研究各种TrkA相关信号中间体在这一调节级联反应中的作用。值得注意的是,使用U73122抑制磷脂酶C-γ(PLC-γ)可阻止NGF诱导的p75NTR蛋白和mRNA上调。选择性PKC-δ抑制剂rottlerin以及针对PKC-δ的小干扰RNA(siRNA)抑制蛋白激酶C-δ(PKC-δ)的激活,也抑制了这种NGF诱导的上调。最后,我们还表明,在小脑颗粒神经元中,通过TrkB起作用的脑源性神经营养因子(BDNF)以PKC-δ依赖的方式增加p75NTR表达。这些结果表明,Trk依赖的PLC-γ和PKC-δ激活对于神经营养因子刺激下p75NTR蛋白表达的下游调节很重要,这一过程对发育中神经系统的存活和生长具有重要意义。

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