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小鼠脑发育过程中单个γ-原钙黏蛋白的差异表达。

Differential expression of individual gamma-protocadherins during mouse brain development.

作者信息

Frank Marcus, Ebert Matthias, Shan Weisong, Phillips Greg R, Arndt Kirsten, Colman David R, Kemler Rolf

机构信息

Department of Molecular Embryology, Max-Planck Institute of Immunobiology, D-79108 Freiburg, Germany.

出版信息

Mol Cell Neurosci. 2005 Aug;29(4):603-16. doi: 10.1016/j.mcn.2005.05.001.

Abstract

Three tandemly arrayed protocadherin gene clusters (Pcdh-alpha, -beta, -gamma) comprising more than 50 genes are found in human and mouse. Here, we have investigated the expression and distribution of individual gamma-protocadherins (Pcdhs-gamma) in the developing mouse brain. We find that transfection of Pcdh-gamma genes promotes calcium-dependent cell adhesion in HEK 293 cells. Furthermore, Pcdh-gamma can be recruited to synapses of transfected primary hippocampal neurons. Several individual members of the in total 22 Pcdhs-gamma were chosen to examine the expression of the three subfamilies, Pcdh-gammaA, -gammaB, and -gammaC. These Pcdh-gamma transcripts are expressed all over the brain, with minor regional and cell-type specific differences. Interestingly, a distinct, later onset of expression is observed for Pcdh-gammaC5, a gene located at the end of the Pcdh-gamma cluster. Largely overlapping expression patterns of individual Pcdh-gamma proteins are detected with anti-peptide antibodies. Small differences are observed in the staining of dendritic processes and synapse-rich layers. Our results support the idea that Pcdhs-gamma participate in neuronal differentiation and may be implicated in the fine-tuning of neuronal morphology and synaptogenesis. Cell autonomous regulation of transcription might generate the widespread distribution of individual Pcdhs-gamma in the brain, which is strikingly different from the restricted expression patterns observed for classical cadherins. Thus, a defined set of Pcdhs-gamma may engage in neuronal adhesion and signaling on the cellular level.

摘要

在人类和小鼠中发现了由50多个基因组成的三个串联排列的原钙黏蛋白基因簇(Pcdh-α、-β、-γ)。在此,我们研究了单个γ-原钙黏蛋白(Pcdhs-γ)在发育中的小鼠大脑中的表达和分布。我们发现,转染Pcdh-γ基因可促进HEK 293细胞中钙依赖性细胞黏附。此外,Pcdh-γ可被募集到转染的原代海马神经元的突触中。从总共22个Pcdhs-γ中选择了几个个体成员来检测三个亚家族Pcdh-γA、-γB和-γC的表达。这些Pcdh-γ转录本在全脑表达,区域和细胞类型特异性差异较小。有趣的是,位于Pcdh-γ簇末端的基因Pcdh-γC5表现出明显较晚的表达起始。用抗肽抗体检测到单个Pcdh-γ蛋白的表达模式在很大程度上重叠。在树突状突起和富含突触的层的染色中观察到微小差异。我们的结果支持这样的观点,即Pcdhs-γ参与神经元分化,并可能与神经元形态和突触形成的微调有关。转录的细胞自主调节可能导致单个Pcdhs-γ在大脑中广泛分布,这与经典钙黏蛋白观察到的受限表达模式明显不同。因此,一组特定的Pcdhs-γ可能在细胞水平上参与神经元黏附和信号传导。

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