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深度测序和高分辨率成像揭示了 Bdnf mRNA 在海马神经元中的隔室特异性定位。

Deep sequencing and high-resolution imaging reveal compartment-specific localization of Bdnf mRNA in hippocampal neurons.

机构信息

Department of Synaptic Plasticity, Max Planck Institute for Brain Research, Max von Laue Strasse 4, 60438 Frankfurt, Germany.

出版信息

Sci Signal. 2013 Dec 17;6(306):rs16. doi: 10.1126/scisignal.2004520.

Abstract

Brain-derived neurotrophic factor (BDNF) is a small protein of the neurotrophin family that regulates various brain functions. Although much is known about how its transcription is regulated, the abundance of endogenous BDNF mRNA and its subcellular localization pattern are matters of debate. We used next-generation sequencing and high-resolution in situ hybridization in the rat hippocampus to reexamine this question. We performed 3' end sequencing on rat hippocampal slices and detected two isoforms of Bdnf containing either a short or a long 3' untranslated region (3'UTR). Most of the Bdnf transcripts contained the short 3'UTR isoform and were present in low amounts relative to other neuronal transcripts. Bdnf mRNA was present in the somatic compartment of rat hippocampal slices or the somata of cultured rat hippocampal neurons but was rarely detected in the dendritic processes. Pharmacological stimulation of hippocampal neurons induced Bdnf expression but did not change the ratio of Bdnf isoform abundance. The findings indicate that endogenous Bdnf mRNA, although weakly abundant, is primarily localized to the somatic compartment of hippocampal neurons. Both Bdnf mRNA isoforms have shorter half-lives compared with other neuronal mRNAs. Furthermore, the findings show that using complementary high-resolution techniques can provide sensitive measures of endogenous transcript abundance.

摘要

脑源性神经营养因子(BDNF)是神经生长因子家族的一种小蛋白,调节各种大脑功能。尽管人们对其转录如何调控有了很多了解,但内源性 BDNF mRNA 的丰度及其亚细胞定位模式仍存在争议。我们使用下一代测序和高分辨率原位杂交技术在大鼠海马体中重新研究了这个问题。我们对大鼠海马切片进行了 3'末端测序,并检测到两种含有短或长 3'非翻译区(3'UTR)的 Bdnf 异构体。大多数 Bdnf 转录本包含短 3'UTR 异构体,与其他神经元转录本相比含量较低。Bdnf mRNA 存在于大鼠海马切片的体细胞区室或培养的大鼠海马神经元的胞体中,但在树突突中很少检测到。海马神经元的药理学刺激诱导 Bdnf 表达,但不会改变 Bdnf 异构体丰度的比值。这些发现表明,尽管内源性 BDNF mRNA 丰度较弱,但主要定位于海马神经元的体细胞区室。与其他神经元 mRNA 相比,两种 Bdnf mRNA 异构体的半衰期都较短。此外,这些发现表明,使用互补的高分辨率技术可以提供对内源性转录物丰度的敏感测量。

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