AGING, BRAIN MEMBRANE CHOLESTEROL DOMAINS AND CALCIUM

衰老、脑膜胆固醇域和钙

• 批准号: 2052268
• 负责人: WELLINGTON GIBSON WOOD
• 金额: $ 24.32万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 1993
• 资助国家: 美国
• 起止时间: 1993-09-30 至 1997-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/2052268
• 关键词: aging; brain metabolism; calcium channel blockers; calcium flux; calcium indicator; calcium transporting ATPase; cell membrane; chemical structure; cholesterol; fatty acid binding protein; homeostasis; laboratory mouse; lipid metabolism; membrane lipids; molecular site; phospholipids; phosphorylation; protein sequence; sphingomyelins; sulfonate; synapses; synaptosomes; thin layer chromatography; western blottings

The overall goals of this grant application are to study potential mechanisms associated with regulation of neuronal transbilayer and lateral cholesterol domains and how cholesterol domains interact with calcium homeostasis in neuronal membranes of different age groups of mice. We have recently shown in synaptic plasma membranes (SPM) of young C57BL mice, that the two membrane leaflets are asymmetric in their fluidity and cholesterol distribution. Membrane cholesterol was also found to be located in exchangeable and non-exchangeable pools and membrane cholesterol domains could be altered by hydrolysis of sphingomyelin that also altered intracellular calcium. Preliminary data from out laboratory showed that the asymmetry of fluidity between the two SPM leaflets observed in 6 month old animals was significantly reduced in SPM of 28 month old animals and that the exofacial leaflet was more affected as compared to the cytofacial leaflet. Previous studies on membrane lipid structure in different age groups of animals have examined changes in the average fluidity of the membrane lipid structure, whereas other studies have not observed age differences. We propose that increasing age is associated with marked changes in membrane lipid structure but that such changes are occurring in specific lipid domains and changes in lipid domains contribute to modification of calcium homeostasis that has been previously shown to differ with increasing age. The proposed experiments will focus on SPM and synaptosomes of 4, 16, and 28 month old C57BL/NNia mice. The specific aims of this application are to: 1) determine transbilayer distribution of cholesterol in the SPM exofacial and cytofacial leaflets; 2) examine cholesterol lateral domains in SPM; 3) phospholipid distribution in SPM exofacial and cytofacial leaflets; 4) involvement of sphingomyelin in regulation of cholesterol domains; 5) brain sterol carrier proteins and regulation of cholesterol domains; and 6) cholesterol domains and presynaptic calcium. It is our working hypothesis that aging impairs the capacity of the membrane to regulate cholesterol domains and such changes in cholesterol domains modify neuronal calcium.

这项赠款申请的总体目标是研究潜力 与神经元跨双层和侧向调节相关的机制 胆固醇结构域及其与钙的相互作用 不同年龄组小鼠神经细胞膜的动态平衡。我们有 最近在幼年C57BL小鼠的突触质膜(SPM)中发现， 这两片膜的流动性是不对称的， 胆固醇的分布。膜胆固醇也被发现是 位于可交换和不可交换的池和膜中 胆固醇区可以通过神经鞘磷脂的水解而改变 也改变了细胞内的钙离子。来自外部实验室的初步数据 表明两个SPM小叶之间的流动性不对称 在6个月大的动物中观察到的28个月的SPM显著减少 一个月大的动物和表面传单受到的影响更大，因为 与细胞面的小叶相比。膜脂的研究进展 不同年龄段的动物的结构检查了 膜脂结构的平均流动性，而其他研究 没有观察到年龄差异。我们认为，年龄的增加是 与膜脂结构的显著变化有关，但这样 在特定的脂域和脂类的变化中正在发生变化 结构域有助于调节钙稳态，而钙稳态 之前的研究表明，随着年龄的增长，这种情况会有所不同。拟议中的实验 将专注于4、16和28个月龄的C57BL/NNia的SPM和突触体 老鼠。本申请的具体目的是：1)确定 胆固醇在SPM表面和胞外的跨双分子层分布 细胞表面小叶；2)检查SPM中的胆固醇侧域；3) 磷脂在SPM面外和细胞面叶中的分布； 鞘磷脂参与胆固醇结构域的调节；5) 大脑类固醇载体蛋白和胆固醇结构域的调节；以及 6)胆固醇结构域和突触前钙。这是我们的工作 衰老削弱细胞膜调节能力的假说 胆固醇结构域和胆固醇结构域的这种变化 神经细胞钙。