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胆固醇调节 Müller 胶质细胞中的多模态感觉转导。

Cholesterol regulates polymodal sensory transduction in Müller glia.

机构信息

Departments of Ophthalmology and Visual Sciences, University of Utah, Salt Lake City, Utah.

Bioengineering, University of Utah, Salt Lake City, Utah.

出版信息

Glia. 2017 Dec;65(12):2038-2050. doi: 10.1002/glia.23213. Epub 2017 Aug 30.

DOI:10.1002/glia.23213
PMID:28856727
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5761668/
Abstract

Over- and underexposure to cholesterol activates glia in neurodegenerative brain and retinal diseases but the molecular targets of cholesterol in glial cells are not known. Here, we report that disruption of unesterified membrane cholesterol content modulates the transduction of chemical, mechanical and temperature stimuli in mouse Müller cells. Activation of TRPV4 (transient receptor potential vanilloid type 4), a nonselective polymodal cation channel was studied following the removal or supplementation of cholesterol using the methyl-beta cyclodextrin (MβCD) delivery vehicle. Cholesterol extraction disrupted lipid rafts and caveolae without affecting TRPV4 trafficking or membrane localization protein. However, MβCD suppressed agonist (GSK1016790A)- and temperature-evoked elevations in [Ca ] , and suppressed transcellular propagation of Ca waves. Lowering the free membrane cholesterol content markedly prolonged the time-course of the glial swelling response, whereas MβCD:cholesterol supplementation enhanced agonist- and temperature-induced Ca signals and shortened the swelling response. Taken together, these data show that membrane cholesterol modulates polymodal transduction of agonists, swelling and temperature stimuli in retinal radial glia and suggest that dyslipidemic retinas might be associated with abnormal glial transduction of ambient sensory inputs.

摘要

胆固醇的过度和不足暴露会激活神经退行性脑和视网膜疾病中的神经胶质细胞,但胆固醇在神经胶质细胞中的分子靶点尚不清楚。在这里,我们报告称,未酯化膜胆固醇含量的破坏会调节小鼠 Muller 细胞中化学、机械和温度刺激的转导。使用甲基-β-环糊精(MβCD)传递载体去除或补充胆固醇后,研究了瞬时受体电位香草醛亚型 4(TRPV4),一种非选择性多模式阳离子通道的激活情况。胆固醇提取会破坏脂筏和 caveolae,但不会影响 TRPV4 转运或膜定位蛋白。然而,MβCD 抑制激动剂(GSK1016790A)和温度引发的 [Ca2+]升高,并抑制 Ca 波的细胞间传播。降低游离膜胆固醇含量会显著延长神经胶质肿胀反应的时程,而 MβCD:胆固醇补充则增强了激动剂和温度诱导的 Ca 信号,并缩短了肿胀反应。总之,这些数据表明,膜胆固醇调节了视网膜放射状胶质细胞中激动剂、肿胀和温度刺激的多模式转导,并表明血脂异常的视网膜可能与环境感觉输入的异常神经胶质转导有关。

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