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EFA6家族的第三个成员EFA6C在成年小鼠浦肯野细胞中的细胞及亚细胞定位。

Cellular and subcellular localization of EFA6C, a third member of the EFA6 family, in adult mouse Purkinje cells.

作者信息

Matsuya Shigetsune, Sakagami Hiroyuki, Tohgo Akira, Owada Yuji, Shin Hye-Won, Takeshima Hiroshi, Nakayama Kazuhisa, Kokubun Shoichi, Kondo Hisatake

机构信息

Division of Histology, Department of Cell Biology, Tohoku University Graduate School of Medicine, Sendai, Japan.

出版信息

J Neurochem. 2005 May;93(3):674-85. doi: 10.1111/j.1471-4159.2005.03072.x.

Abstract

EFA6C is a third member of the EFA6 family of guanine nucleotide exchange factors (GEFs) for ADP-ribosylation factor 6 (ARF6). In this study, we first demonstrated that EFA6C indeed activated ARF6 more selectively than ARF1 by ARF pull-down assay. In situ hybridization histochemistry revealed that EFA6C mRNA was expressed predominantly in mature Purkinje cells and the epithelial cells of the choroid plexus in contrast to the ubiquitous expression of ARF6 mRNA throughout the brain. EFA6C mRNA was already detectable in the Purkinje cells at embryonic day 13, increased progressively during post-natal development and peaked during post-natal second week. In Purkinje cells, the immunoreactivity for EFA6C was localized particularly in the post-synaptic density as well as the plasma membranes of the cell somata, dendritic shafts and spines, while the immunoreactivity in their axon terminals in the deep cerebellar nuclei was very faint. These findings suggest that EFA6C may be involved in the regulation of the membrane dynamics of the somatodendritic compartments of Purkinje cells through the activation of ARF6.

摘要

EFA6C是用于ADP核糖基化因子6(ARF6)的鸟嘌呤核苷酸交换因子(GEF)的EFA6家族的第三个成员。在本研究中,我们首先通过ARF下拉试验证明,EFA6C确实比ARF1更具选择性地激活ARF6。原位杂交组织化学显示,与ARF6 mRNA在整个大脑中的普遍表达相反,EFA6C mRNA主要在成熟的浦肯野细胞和脉络丛上皮细胞中表达。在胚胎第13天,浦肯野细胞中已可检测到EFA6C mRNA,在出生后发育过程中逐渐增加,并在出生后第二周达到峰值。在浦肯野细胞中,EFA6C的免疫反应性特别定位于突触后密度以及细胞体、树突干和棘的质膜,而其在小脑深部核团轴突终末的免疫反应性非常微弱。这些发现表明,EFA6C可能通过激活ARF6参与浦肯野细胞体树突区膜动力学的调节。

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