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p75神经营养因子受体的脱落受脂筏调节。

Shedding of the p75NTR neurotrophin receptor is modulated by lipid rafts.

作者信息

Gil Carles, Cubí Roger, Aguilera José

机构信息

Departament de Bioquímica i Biologia Molecular and Institut de Neurociències, Edifici M, Universitat Autònoma de Barcelona, Bellaterra 08193, Barcelona, Catalunya, Spain.

出版信息

FEBS Lett. 2007 May 1;581(9):1851-8. doi: 10.1016/j.febslet.2007.03.080. Epub 2007 Apr 9.

Abstract

Protein ectodomain shedding is the proteolytic release of the extracellular domain of membrane-bound proteins. Neurotrophin receptor p75(NTR) is known to be affected by shedding. The present work provides evidence, in rat brain synaptosomes, that p75(NTR) is present in detergent-resistant membranes (DRM), also known as lipid rafts, only in its full-length form. Disrupting the integrity of lipid rafts causes solubilization of p75(NTR) after detergent treatment and enhancement of the shedding. Analyses of the enzymes described as being responsible for p75(NTR) shedding, i.e. tumor necrosis factor alpha convertase (TACE) and presenilin-1 (PS1), revealed that TACE is absent in DRM, while variable proportions of the C-terminal and N-terminal fragments of PS1 are found. In summary, our results point to a role of lipid rafts in the modulation of the shedding of the p75(NTR) receptor.

摘要

蛋白质胞外域脱落是膜结合蛋白胞外域的蛋白水解释放。已知神经营养因子受体p75(NTR)会受到脱落的影响。目前的研究工作在大鼠脑突触体中提供了证据,即p75(NTR)仅以其全长形式存在于抗去污剂膜(DRM)中,也称为脂筏。破坏脂筏的完整性会导致去污剂处理后p75(NTR)溶解并增强脱落。对被认为负责p75(NTR)脱落的酶,即肿瘤坏死因子α转化酶(TACE)和早老素-1(PS1)的分析表明,DRM中不存在TACE,而PS1的C末端和N末端片段存在不同比例。总之,我们的结果表明脂筏在调节p75(NTR)受体脱落中起作用。

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