Endocytosis of insulin at the blood-brain barrier.

Frontiers in drug delivery Pub Date : 2022-01-01 Epub Date: 2022-11-24 DOI:10.3389/fddev.2022.1062366
Sarah Pemberton, Demi C Galindo, Michael W Schwartz, William A Banks, Elizabeth M Rhea
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Abstract

For insulin to act within the brain, it is primarily transported from the blood across the blood-brain barrier (BBB). However, the endocytic machinery necessary for delivering insulin to the brain remains unknown. Additionally, there are processes within the brain endothelial cell that are designed to respond to insulin binding and elicit intracellular signaling. Using pharmacological inhibitors of different types of endocytosis (clathrin-vs. caveolin-mediated), we investigated molecular mediators of both insulin BBB binding in isolated mouse brain microvessels and BBB insulin transport in mice studied by brain perfusion. We found clathrin-mediated mechanisms responsible for insulin surface binding in isolated brain microvessels while caveolin-mediated endocytosis may mediate BBB insulin transport specifically in the hypothalamus. These results further define the molecular machinery necessary for transporting insulin into the CNS and highlight the distinction between insulin internalization for transendothelial transport vs. intracellular signaling.

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胰岛素在血脑屏障的内分泌作用
胰岛素要在大脑中起作用,首先要从血液中穿过血脑屏障(BBB)。然而,将胰岛素输送到大脑所需的内吞机制仍不清楚。此外,在脑内皮细胞中有一些过程被设计成对胰岛素结合做出反应并引发细胞内信号传导。使用不同类型内吞作用的药理学抑制剂(网格蛋白vs。我们研究了离体小鼠脑微血管中胰岛素血脑屏障结合和脑灌注小鼠血脑屏障胰岛素转运的分子介质。我们发现网格蛋白介导的机制负责胰岛素在分离的脑微血管表面结合,而小窝蛋白介导的内吞作用可能介导血脑屏障胰岛素转运,特别是在下丘脑。这些结果进一步明确了胰岛素转运到中枢神经系统所需的分子机制,并强调了胰岛素内化的跨内皮转运与细胞内信号传导之间的区别。
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