Laboratory of Biophysics, Department of Condensed Matter Physics, Jožef Stefan Institute, 1000 Ljubljana, Slovenia.
Veterinary Faculty, Institute of Preclinical Sciences, University of Ljubljana, Gerbičeva 60, 1000 Ljubljana, Slovenia.
Molecules. 2021 Feb 12;26(4):973. doi: 10.3390/molecules26040973.
This study investigated the effect of type 1 gonadotropin releasing hormone receptor (GnRH-R) localization within lipid rafts on the properties of plasma membrane (PM) nanodomain structure. Confocal microscopy revealed colocalization of PM-localized GnRH-R with GM-enriched raft-like PM subdomains. Electron paramagnetic resonance spectroscopy (EPR) of a membrane-partitioned spin probe was then used to study PM fluidity of immortalized pituitary gonadotrope cell line αT3-1 and HEK-293 cells stably expressing GnRH-R and compared it with their corresponding controls (αT4 and HEK-293 cells). Computer-assisted interpretation of EPR spectra revealed three modes of spin probe movement reflecting the properties of three types of PM nanodomains. Domains with an intermediate order parameter (domain 2) were the most affected by the presence of the GnRH-Rs, which increased PM ordering (order parameter (S)) and rotational mobility of PM lipids (decreased rotational correlation time (τc)). Depletion of cholesterol by methyl-β-cyclodextrin (methyl-β-CD) inhibited agonist-induced GnRH-R internalization and intracellular Ca activity and resulted in an overall reduction in PM order; an observation further supported by molecular dynamics (MD) simulations of model membrane systems. This study provides evidence that GnRH-R PM localization may be related to a subdomain of lipid rafts that has lower PM ordering, suggesting lateral heterogeneity within lipid raft domains.
本研究探讨了 1 型促性腺激素释放激素受体(GnRH-R)在脂筏内的定位对质膜(PM)纳米域结构特性的影响。共焦显微镜显示 PM 定位的 GnRH-R 与富含 GM 的脂筏样 PM 亚域共定位。然后,使用膜分离的自旋探针的电子顺磁共振波谱(EPR)研究了稳定表达 GnRH-R 的永生化垂体促性腺激素细胞系αT3-1 和 HEK-293 细胞以及相应对照(αT4 和 HEK-293 细胞)的 PM 流动性。EPR 光谱的计算机辅助解释揭示了三种旋转探针运动模式,反映了三种类型的 PM 纳米域的特性。具有中间序参数(域 2)的域受 GnRH-Rs 的存在影响最大,这增加了 PM 的有序性(序参数(S))和 PM 脂质的旋转流动性(旋转相关时间(τc)减小)。用甲基-β-环糊精(methyl-β-CD)耗尽胆固醇抑制了激动剂诱导的 GnRH-R 内化和细胞内 Ca 活性,并导致 PM 有序性总体降低;这一观察结果得到了模型膜系统的分子动力学(MD)模拟的进一步支持。本研究提供的证据表明,GnRH-R PM 定位可能与脂筏的亚域有关,该亚域的 PM 有序性较低,表明脂筏域内存在横向异质性。