Suppr超能文献

脑源性神经营养因子诱导的神经元可塑性的转录谱分析:孤啡肽在海马神经突生长中的新作用。

Transcriptional profiling of brain-derived-neurotrophic factor-induced neuronal plasticity: a novel role for nociceptin in hippocampal neurite outgrowth.

作者信息

Ring Robert H, Alder Janet, Fennell Myles, Kouranova Evguenia, Black Ira B, Thakker-Varia Smita

机构信息

Wyeth Research, Discovery Neuroscience, CN8000, Princeton, New Jersey 08543, USA.

出版信息

J Neurobiol. 2006 Mar;66(4):361-77. doi: 10.1002/neu.20223.

Abstract

Brain derived neurotrophic factor (BDNF) exhibits a sequence of actions on neurons ranging from acute enhancement of transmission to long-term promotion of neurite outgrowth and synaptogenesis associated with learning and memory. The manifold effects of BDNF on neuronal modifications may be mediated by genomic alterations. We previously found that BDNF treatment acutely increases transcription of the synaptic vesicle protein Rab3A, required for trophin-induced synaptic plasticity, as well as the peptide VGF, which increases during learning. To elucidate comprehensive transcriptional programs associated with short- and long-term BDNF exposure, we now examine mRNA abundance and complexity using Affymetrix GeneChips in cultured hippocampal neurons. Consistent with the modulation of synaptic plasticity, BDNF treatment (3-6 h) induced mRNAs encoding the synapse-associated proteins synaptojanin 2, neuronal pentraxin 1, septin 9, and ryanodine receptor 2. BDNF also induced expression of mRNAs encoding neuropeptides (6-12 h), including prepronociceptin, neuropeptide Y, and secretogranin. To determine whether these neuropeptides induced by BDNF mediate neuronal development, we examined their effects on hippocampal neurons. The four mature peptides derived from post-translational processing of the ppNociceptin propeptide induced the expression of several immediate early genes in hippocampal cultures, indicating neuronal activation. To examine the significance of activation, the effects of nociceptin (orphanin FQ) and nocistatin on neurite outgrowth were examined. Quantitative morphometric analysis revealed that nociceptin significantly increased both average neurite length and average number of neurites per neuron, while nocistatin had no effect on these parameters. These results reveal a novel role for nociceptin and suggest that these neuropeptide systems may contribute to the regulation of neuronal function by BDNF.

摘要

脑源性神经营养因子(BDNF)对神经元具有一系列作用,从急性增强神经传递到长期促进与学习和记忆相关的神经突生长和突触形成。BDNF对神经元修饰的多种作用可能由基因组改变介导。我们之前发现,BDNF处理可急性增加突触囊泡蛋白Rab3A的转录,Rab3A是神经营养因子诱导的突触可塑性所必需的,同时也可增加学习过程中增加的肽VGF的转录。为了阐明与短期和长期BDNF暴露相关的全面转录程序,我们现在使用Affymetrix基因芯片检测培养的海马神经元中的mRNA丰度和复杂性。与突触可塑性的调节一致,BDNF处理(3 - 6小时)诱导了编码突触相关蛋白突触素2、神经元五聚体蛋白1、septin 9和兰尼碱受体2的mRNA。BDNF还诱导了编码神经肽(6 - 12小时)的mRNA的表达,包括前痛敏肽原、神经肽Y和分泌粒蛋白。为了确定BDNF诱导的这些神经肽是否介导神经元发育,我们检测了它们对海马神经元的影响。痛敏肽原前体肽经翻译后加工产生的四种成熟肽在海马培养物中诱导了几种立即早期基因的表达,表明神经元被激活。为了检测激活的意义,我们检测了痛敏肽(孤啡肽FQ)和痛抑素对神经突生长的影响。定量形态计量分析显示,痛敏肽显著增加了每个神经元的平均神经突长度和平均神经突数量,而痛抑素对这些参数没有影响。这些结果揭示了痛敏肽的新作用,并表明这些神经肽系统可能有助于BDNF对神经元功能的调节。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验