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BAG3参与神经元的分化和迁移。

BAG3 is involved in neuronal differentiation and migration.

作者信息

Santoro Antonietta, Nicolin Vanessa, Florenzano Fulvio, Rosati Alessandra, Capunzo Mario, Nori Stefania L

机构信息

Department of Medicine, Surgery and Dentistry, "Scuola Medica Salernitana", University of Salerno, Salerno, Italy.

Clinical Department of Medical, Surgical and Health Science, University of Trieste, Trieste, Italy.

出版信息

Cell Tissue Res. 2017 May;368(2):249-258. doi: 10.1007/s00441-017-2570-7. Epub 2017 Feb 1.

Abstract

Bcl2-associated athanogene 3 (BAG3) protein belongs to the family of co-chaperones interacting with several heat shock proteins. It plays a key role in protein quality control and mediates the clearance of misfolded proteins. Little is known about the expression and cellular localization of BAG3 during nervous system development and differentiation. Therefore, we analyze the subcellular distribution and expression of BAG3 in nerve-growth-factor-induced neurite outgrowth in PC12 cells and in developing and adult cortex of mouse brain. In differentiated PC12 cells, BAG3 was localized mainly in the neuritic domain rather than the cell body, whereas in control cells, it appeared to be confined to the cytoplasm near the nuclear membrane. Interestingly, the change of BAG3 localization during neuronal differentiation was associated only with a slight increase in total BAG3 expression. These data were coroborated by transmission electron microscopy showing that BAG3 was confined mainly within large dense-core vesicles of the axon in differentiated PC12 cells. In mouse developing cortex, BAG3 appeared to be intensely expressed in cellular processes of migrating cells, whereas in adult brain, a diffuse expression of low to medium intensity was detected in neuronal cell bodies. These findings suggest that BAG3 expression is required for neuronal differentiation and migration and that its role is linked to a change in its distribution pattern rather than to an increase in its protein expression levels.

摘要

Bcl2相关抗凋亡基因3(BAG3)蛋白属于与多种热休克蛋白相互作用的共伴侣蛋白家族。它在蛋白质质量控制中起关键作用,并介导错误折叠蛋白的清除。关于BAG3在神经系统发育和分化过程中的表达及细胞定位知之甚少。因此,我们分析了BAG3在神经生长因子诱导的PC12细胞神经突生长以及小鼠脑发育中和成年期皮质中的亚细胞分布及表达情况。在分化的PC12细胞中,BAG3主要定位于神经突区域而非细胞体,而在对照细胞中,它似乎局限于核膜附近的细胞质中。有趣的是,神经元分化过程中BAG3定位的变化仅与BAG3总表达量的轻微增加有关。这些数据通过透射电子显微镜得到证实,显示在分化的PC12细胞中BAG3主要局限于轴突的大致密核心囊泡内。在小鼠发育中的皮质中,BAG3似乎在迁移细胞的细胞突起中强烈表达,而在成年脑中,在神经元细胞体中检测到低至中等强度的弥漫性表达。这些发现表明,BAG3的表达是神经元分化和迁移所必需的,并且其作用与分布模式的改变而非蛋白质表达水平的增加有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32dd/5397659/ecbdb042b14d/441_2017_2570_Fig1_HTML.jpg

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