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少突胶质细胞突起的形成受到调节细胞内外胆固醇含量的影响而出现差异。

Oligodendroglial process formation is differentially affected by modulating the intra- and extracellular cholesterol content.

机构信息

Max-Planck Institute of Experimental Medicine, RU Neural Regeneration, Hermann-Rein-Straße 3, 37075, Goettingen, Germany.

出版信息

J Mol Neurosci. 2013 Mar;49(3):457-69. doi: 10.1007/s12031-012-9833-2. Epub 2012 Jun 28.

Abstract

Cholesterol is an essential component of eukaryotic plasma membranes and plays an important role in membrane organization and signaling processes. It is the major lipid component of detergent resistant caveolin-1 containing rafts which previously had been reported as a platform for nerve growth factor (NGF) signaling in oligodendrocytes (OL). Surprisingly, a knockdown of caveolin-1 attenuated the process formation of OL (Schmitz et al. J Neurosci Res 88:572-588, 2010), for which a loss of cholesterol could be responsible. In the present report, we could show that a caveolin-1 knockdown resulted in an elevation of cellular cholesterol level; it may indicate an important role of caveolin-1 in cholesterol trafficking to the plasma membrane. Treatment with exogenous PEG cholesterol, which was incorporated to the plasma membrane, supported oligodendroglial process formation, in particular when OL were stimulated by NGF. In this context we have found that OL express NPC1L1 (Niemann-Pick disease type C1-Like 1) which could modulate cholesterol uptake. In contrast, depletion of membrane-bound cholesterol diminished NGF-induced process formation concomitant with a reduced activity of p42/44 mitogen-activated protein kinases.

摘要

胆固醇是真核质膜的重要组成部分,在膜组织和信号转导过程中发挥着重要作用。它是包含窖蛋白-1(caveolin-1)的去污剂抗性小窝(detergent resistant caveolin-1 containing rafts)的主要脂质成分,先前曾被报道为少突胶质细胞(oligodendrocytes,OL)中神经生长因子(nerve growth factor,NGF)信号的平台。令人惊讶的是,caveolin-1 的敲低会减弱 OL 的突起形成过程(Schmitz 等人,J Neurosci Res 88:572-588, 2010),胆固醇的缺失可能是造成这种情况的原因。在本报告中,我们可以证明 caveolin-1 的敲低会导致细胞内胆固醇水平升高;这可能表明 caveolin-1 在胆固醇向质膜转运中起着重要作用。用外源性 PEG 胆固醇(可整合到质膜中)处理可支持少突胶质细胞突起的形成,尤其是在 NGF 刺激 OL 时。在这种情况下,我们发现 OL 表达 NPC1L1(尼曼-匹克病 C1 样 1),它可以调节胆固醇摄取。相反,膜结合胆固醇的耗竭会减少 NGF 诱导的突起形成,同时 p42/44 丝裂原活化蛋白激酶的活性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fff/3566395/45f4f15f78ca/12031_2012_9833_Fig1_HTML.jpg

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