Department of Biological Sciences, The George Washington University, Washington, D. C. 20052.
Department of Biological Sciences, The George Washington University, Washington, D. C. 20052.
J Biol Chem. 2011 Oct 14;286(41):36086-36097. doi: 10.1074/jbc.M111.240762. Epub 2011 Aug 24.
Self-assembly of the human pancreatic hormone amylin into toxic oligomers and aggregates is linked to dysfunction of islet β-cells and pathogenesis of type 2 diabetes mellitus. Recent evidence suggests that cholesterol, an essential component of eukaryotic cells membranes, controls amylin aggregation on model membranes. However, the pathophysiological consequence of cholesterol-regulated amylin polymerization on membranes and biochemical mechanisms that protect β-cells from amylin toxicity are poorly understood. Here, we report that plasma membrane (PM) cholesterol plays a key role in molecular recognition, sorting, and internalization of toxic amylin oligomers but not monomers in pancreatic rat insulinoma and human islet cells. Depletion of PM cholesterol or the disruption of the cytoskeleton network inhibits internalization of amylin oligomers, which in turn enhances extracellular oligomer accumulation and potentiates amylin toxicity. Confocal microscopy reveals an increased nucleation of amylin oligomers across the plasma membrane in cholesterol-depleted cells, with a 2-fold increase in cell surface coverage and a 3-fold increase in their number on the PM. Biochemical studies confirm accumulation of amylin oligomers in the medium after depletion of PM cholesterol. Replenishment of PM cholesterol from intracellular cholesterol stores or by the addition of water-soluble cholesterol restores amylin oligomer clustering at the PM and internalization, which consequently diminishes cell surface coverage and toxicity of amylin oligomers. In contrast to oligomers, amylin monomers followed clathrin-dependent endocytosis, which is not sensitive to cholesterol depletion. Our studies identify an actin-mediated and cholesterol-dependent mechanism for selective uptake and clearance of amylin oligomers, impairment of which greatly potentiates amylin toxicity.
人胰腺激素胰岛淀粉样多肽自组装成毒性寡聚体和聚集体与胰岛 β 细胞功能障碍和 2 型糖尿病的发病机制有关。最近的证据表明,胆固醇是真核细胞膜的重要组成部分,控制模型膜上的胰岛淀粉样多肽聚集。然而,胆固醇调节的胰岛淀粉样多肽在膜上聚合的病理生理后果以及保护β细胞免受胰岛淀粉样多肽毒性的生化机制尚不清楚。在这里,我们报告质膜(PM)胆固醇在胰腺大鼠胰岛素瘤和人胰岛细胞中有毒胰岛淀粉样多肽寡聚体但不是单体的分子识别、分类和内化中起关键作用。PM 胆固醇的耗竭或细胞骨架网络的破坏抑制了胰岛淀粉样多肽寡聚体的内化,这反过来又增强了细胞外寡聚体的积累并增强了胰岛淀粉样多肽的毒性。共聚焦显微镜显示,在胆固醇耗尽的细胞中,胰岛淀粉样多肽寡聚体在质膜上的成核增加,细胞表面覆盖率增加 2 倍,其在质膜上的数量增加 3 倍。生化研究证实,在耗尽 PM 胆固醇后,胰岛淀粉样多肽寡聚体在培养基中积累。从细胞内胆固醇库或添加水溶性胆固醇补充 PM 胆固醇可恢复质膜上胰岛淀粉样多肽寡聚体的聚集和内化,从而减少细胞表面覆盖度和胰岛淀粉样多肽寡聚体的毒性。与寡聚体不同,胰岛淀粉样多肽单体遵循网格蛋白依赖性内吞作用,其对胆固醇耗竭不敏感。我们的研究确定了一种肌动蛋白介导的和胆固醇依赖性的机制,用于选择性摄取和清除胰岛淀粉样多肽寡聚体,其功能障碍极大地增强了胰岛淀粉样多肽的毒性。