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极性蛋白 CRB2 在成年小鼠大脑中的表达和定位:与 CRB1 突变体小鼠模型的比较。

Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1 mutant mouse model.

机构信息

Institute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.

Department of Ophthalmology and Stein Eye Institute, University of California, Los Angeles, CA, 90095, USA.

出版信息

Sci Rep. 2018 Aug 3;8(1):11652. doi: 10.1038/s41598-018-30210-5.

Abstract

Acquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, identified in mammals, are expressed in epithelial-derived tissues like brain, kidney and retina. CRB2 has a ubiquitous expression and has been detected in embryonic brain tissue; but currently there is no data regarding its localization in the adult brain. In our study, we characterized the presence of CRB2 in adult mice brain, where it is particularly enriched in cortex, hippocampus, hypothalamus and cerebellum. Double immunofluorescence analysis confirmed that CRB2 is a neuron-specific protein, present in both soma and projections where colocalizes with certain populations of exocytic and endocytic vesicles and with other members of the Crumbs complex. Finally, in the cortex of CRB1 mutant mice that contain a mutation in the Crb1 gene generating a truncated CRB1 protein, there is an abnormal increase in the expression levels of the CRB2 protein which suggests a possible compensatory mechanism for the malfunction of CRB1 in this mutant background.

摘要

细胞极化的获得对于许多组织中关键功能的发挥至关重要,例如成功的分泌和适当的细胞信号转导,这取决于极性蛋白的正确功能,包括 Crumbs 复合物。在哺乳动物中鉴定出的 CRB 蛋白,CRB1、CRB2 和 CRB3,在脑、肾和视网膜等上皮来源的组织中表达。CRB2 具有广泛的表达,在胚胎脑组织中被检测到;但目前尚无关于其在成年大脑中定位的资料。在我们的研究中,我们描述了 CRB2 在成年小鼠大脑中的存在,它在大脑皮层、海马体、下丘脑和小脑中有特别丰富的表达。双重免疫荧光分析证实 CRB2 是一种神经元特异性蛋白,存在于体和突起中,与某些外排和内吞小泡的群体以及 Crumbs 复合物的其他成员共定位。最后,在 Crb1 基因发生突变导致截短 CRB1 蛋白的 CRB1 突变小鼠的皮层中,CRB2 蛋白的表达水平异常增加,这表明在这种突变背景下,CRB1 功能障碍可能存在一种补偿机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16af/6076319/5adacaedb238/41598_2018_30210_Fig1_HTML.jpg

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