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VAMP7/TI-VAMP 在细胞极性和溶酶体胞吐中的作用。

The role of VAMP7/TI-VAMP in cell polarity and lysosomal exocytosis in vivo.

机构信息

Department of Cellular and Molecular Biology, Laboratory for Molecular Traffic, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi 371-8512, Japan.

出版信息

Traffic. 2011 Oct;12(10):1383-93. doi: 10.1111/j.1600-0854.2011.01247.x. Epub 2011 Aug 5.

Abstract

VAMP7 or tetanus neurotoxin-insensitive vesicle- associated membrane protein (TI-VAMP) has been proposed to regulate apical transport in polarized epithelial cells, axonal transport in neurons and lysosomal exocytosis. To investigate the function of VAMP7 in vivo, we generated VAMP7 knockout mice. Here, we show that VAMP7 knockout mice are indistinguishable from control mice and display a similar localization of apical proteins in the kidney and small intestine and a similar localization of axonal proteins in the nervous system. Neurite outgrowth of cultured mutant hippocampal neurons was reduced in mutant neurons. However, lysosomal exocytosis was not affected in mutant fibroblasts. Our results show that VAMP7 is required in neurons to extend axons to the full extent. However, VAMP7 does not seem to be required for epithelial cell polarity and lysosomal exocytosis.

摘要

VAMP7 或破伤风神经毒素不敏感囊泡相关膜蛋白(TI-VAMP)被提议调节极化上皮细胞中的顶端转运、神经元中的轴突转运和溶酶体胞吐。为了研究 VAMP7 在体内的功能,我们生成了 VAMP7 敲除小鼠。在这里,我们表明 VAMP7 敲除小鼠与对照小鼠没有区别,并且在肾脏和小肠中观察到类似的顶端蛋白定位,在神经系统中观察到类似的轴突蛋白定位。培养的突变海马神经元的神经突生长在突变神经元中减少。然而,突变成纤维细胞中的溶酶体胞吐作用没有受到影响。我们的结果表明,VAMP7 是神经元延伸轴突到全长所必需的。然而,VAMP7 似乎不需要用于上皮细胞极性和溶酶体胞吐作用。

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