Regulation of various proteolytic pathways by insulin and amino acids in human fibroblasts

被引:13
作者
Esteban, Inmaculada
Aguado, Carmen
Sanchez, Maribel
Knecht, Erwin
机构
[1] Ctr Invest Principle Felipe, Lab Biol Celular, Ctr Invest Principe, Valencia 46013, Spain
[2] CIBERER, Valencia, Spain
关键词
intracellular protein degradation; insulin; amino acids; mTOR; lysosomes; proteasomes; human fibroblasts; CHAPERONE-MEDIATED AUTOPHAGY; ISOLATED RAT HEPATOCYTES; PROTEASOME ACTIVITY; PROTEIN-METABOLISM; GROWTH-CONDITIONS; MAMMALIAN-CELLS; C2C12; MYOTUBES; DEGRADATION; MTOR; INHIBITION;
D O I
10.1016/j.febslet.2007.06.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular protein degradation is a regulated process with several proteolytic pathways. Although regulation of macroautophagy has been investigated in some detail in hepatocytes and in few other cells, less is known on this regulation in other cells and proteolytic pathways. We show that in human fibroblasts insulin and amino acids reduce protein degradation by different signalling pathways and that this inhibition proceeds in part via the mammalian target of rapamycin, especially with amino acids, which probably increase lysosomal pH. Moreover, the regulatory amino acids (Phe, Arg, Met, Tyr, Trp and Cys) are partially different from other cells. Finally, and in addition to macroautophagy, insulin and amino acids modify, to different extents and sometimes in opposite directions, the activities of other proteolytic pathways. (c) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:3415 / 3421
页数:7
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