Saito Akihiko, Sato Hiroyoshi, Iino Noriaki, Takeda Tetsuro
Department of Applied Molecular Medicine, Niigata University Graduate School of Medical and Dental Sciences, Chuo-ku, Niigata 951-8510, Japan.
J Biomed Biotechnol. 2010;2010:403272. doi: 10.1155/2010/403272.
Receptor-mediated endocytosis is a pivotal function of renal proximal tubule epithelial cells (PTECs) to reabsorb and metabolize substantial amounts of proteins and other substances in glomerular filtrates. The function accounts for the conservation of nutrients, including carrier-bound vitamins and trace elements, filtered by glomeruli. Impairment of the process results in a loss of such substances and development of proteinuria, an important clinical sign of kidney disease and a risk marker for cardiovascular disease. Megalin is a multiligand endocytic receptor expressed at clathrin-coated pits of PTEC, playing a central role in the process. Megalin cooperates with various membrane molecules and interacts with many intracellular adaptor proteins for endocytic trafficking. Megalin is also involved in signaling pathways in the cells. Megalin-mediated endocytic overload leads to damage of PTEC. Further studies are needed to elucidate the mechanism of megalin-mediated endocytosis and develop strategies for preventing the damage of PTEC.
受体介导的内吞作用是肾近端小管上皮细胞(PTECs)的一项关键功能,可重吸收和代谢肾小球滤液中的大量蛋白质及其他物质。该功能有助于保留肾小球滤过的营养物质,包括与载体结合的维生素和微量元素。这一过程受损会导致此类物质流失并引发蛋白尿,蛋白尿是肾脏疾病的重要临床体征以及心血管疾病的风险标志物。巨蛋白是一种多配体内吞受体,表达于PTEC的网格蛋白包被小窝,在该过程中起核心作用。巨蛋白与多种膜分子协同作用,并与许多细胞内衔接蛋白相互作用以进行内吞运输。巨蛋白还参与细胞内的信号通路。巨蛋白介导的内吞超载会导致PTEC损伤。需要进一步研究以阐明巨蛋白介导的内吞作用机制,并制定预防PTEC损伤的策略。