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缺乏高度丰富的浦肯野细胞和双极神经元特异性PCP2蛋白的小鼠的表型分析。

Phenotypic analysis of mice lacking the highly abundant Purkinje cell- and bipolar neuron-specific PCP2 protein.

作者信息

Mohn A R, Feddersen R M, Nguyen M S, Koller B H

机构信息

Curriculum in Genetics and Molecular Biology, University of North Carolina at Chapel Hill 27599, USA.

出版信息

Mol Cell Neurosci. 1997 Jan;9(1):63-76. doi: 10.1006/mcne.1997.0606.

Abstract

The Purkinje cell protein-2 (Pcp2, also known as L7) gene is abundantly expressed only in Purkinje cells of the cerebellum and bipolar neurons of the retina. The spatio-temporal expression pattern of this gene suggests a role for PCP2 in Purkinje cell development or normal cell physiology. A PCP2-deficient mouse was created by gene targeting to test the hypothesis that it is required for Purkinje cell development or function. Although normally present in abundance, the absence of PCP2 in null animals caused no observable cerebellar abnormalities. Behavioral analysis reveals normal abilities for balance and coordination. Null cerebellum has normal Purkinje cell numbers, morphology, and ultrastructure. Retinal bipolar neurons appear similarly unaffected. Aged null animals (22 months) were also examined and no deficits were detected using the same behavioral and histologic analyses. Although the null animal does not reveal the function of PCP2, it does rule out an essential role for PCP2 in Purkinje cell development, in Purkinje cell survival, and in at least some aspects of cerebellar function.

摘要

浦肯野细胞蛋白2(Pcp2,也称为L7)基因仅在小脑的浦肯野细胞和视网膜的双极神经元中大量表达。该基因的时空表达模式表明PCP2在浦肯野细胞发育或正常细胞生理学中发挥作用。通过基因靶向创建了一只PCP2缺陷小鼠,以检验其对浦肯野细胞发育或功能是必需的这一假设。尽管正常情况下PCP2大量存在,但基因敲除动物中PCP2的缺失并未导致可观察到的小脑异常。行为分析显示平衡和协调能力正常。基因敲除小鼠的小脑浦肯野细胞数量、形态和超微结构正常。视网膜双极神经元似乎同样未受影响。还对老龄基因敲除动物(22个月)进行了检查,使用相同的行为和组织学分析未发现缺陷。尽管基因敲除动物并未揭示PCP2的功能,但它确实排除了PCP2在浦肯野细胞发育、浦肯野细胞存活以及小脑功能的至少某些方面的重要作用。

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