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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Spatio-temporal heterogeneity and cell-specificity of long-term potentiation-induced mRNA expression in the dentate gyrus in vivo.
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Spatio-temporal heterogeneity and cell-specificity of long-term potentiation-induced mRNA expression in the dentate gyrus in vivo.

机译:时空异质性和长期特异性诱导的齿状回体内mRNA表达的细胞特异性。

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摘要

Gene expression in neurones can vary in response to neuronal activation. In this study, to analyse the spatio-temporal dynamics of the transcriptional response of three genes following the induction of long-term potentiation within the entire dentate gyrus in vivo, two new complementary approaches based on in situ hybridisation were developed: three-dimensional reconstruction of the pattern of mRNA expression within the entire dentate gyrus; and radioactive co-detection of two mRNA species allowing quantification of two different mRNAs in the same brain section. Zif268, Homer and syntaxin 1B genes were studied, and their regulated expression was examined three times after the induction of long-term potentiation. Constitutive expression of each gene under control conditions was homogeneous, but the spatial distribution of mRNA was heterogeneous along the rostro-caudal axis of the dentate gyrus following the induction of long-term potentiation, and different for each gene. In addition, the intensity of each gene-specific pattern of expression varied over time following the induction of long-term potentiation. Our results reveal that long-term potentiation differentially modulates the expression of mRNA species in cells of the dentate gyrus depending on their position along the rostro-caudal axis, on the gene and on time. We suggest that there are several molecular mechanisms of long-term potentiation, differing from one cluster of cells of the dentate gyrus to another, or that the different signaling pathways involved in long-term potentiation are used with varying efficiencies by different cells.
机译:神经元中的基因表达可以响应神经元激活而变化。在这项研究中,为了分析在整个齿状回体内长期增强后三个基因转录应答的时空动态,开发了两种基于原位杂交的新互补方法:三维重建整个齿状回中的mRNA表达模式;以及对两种mRNA的放射性共检测,可以定量同一大脑切片中两种不同的mRNA。研究了Zif268,Homer和syntaxin 1B基因,并在诱导长时程增强后三遍检查了它们的调控表达。在控制条件下,每个基因的组成型表达是同质的,但是在长期诱导后,mRNA的空间分布沿齿状回的rostro-caudal-caudal尾轴是异质的,并且每个基因都不同。另外,在诱导长期增强后,每种基因特异性表达模式的强度随时间变化。我们的研究结果表明,长期增强可能会影响齿状回细胞中沿头尾尾轴的位置,基因和时间上mRNA种类的表达。我们建议,存在长时程增强的几种分子机制,从齿状回的一个细胞簇到另一簇细胞,或长时程增强所涉及的不同信号途径被不同的细胞以不同的效率使用。

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