Short term exposure to elevated levels of leptin reduces proximal tubule cell metabolic activity

被引:14
作者
Briffa, Jessica F. [1 ,2 ]
Grinfeld, Esther [1 ]
McAinch, Andrew J. [1 ]
Poronnik, Philip [3 ]
Hryciw, Deanne H. [1 ,2 ]
机构
[1] Victoria Univ, Coll Hlth & Biomed, Biomed & Lifestyle Dis BioLED Unit, St Albans, Vic 3021, Australia
[2] Univ Melbourne, Dept Physiol, Parkville, Vic 3010, Australia
[3] Univ Sydney, Bosch Inst, Sch Med Sci, Sydney, NSW 2006, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Leptin; Kidney; Proximal tubule; Metabolic activity; p44/42; MAPK; ADIPOSE-TISSUE; MEGALIN; HYPERTROPHY; PROTEOLYSIS; ENDOCYTOSIS; INFUSION; EXCHANGE; ORGAN;
D O I
10.1016/j.mce.2013.09.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Leptin plays a pathophysiological role in the kidney, however, its acute effects on the proximal tubule cells (PTCs) are unknown. In opossum kidney (OK) cells in vitro, Western blot analysis identified that exposure to leptin increases the phosphorylation of the mitogen-activated protein kinase (MAPK) p44/42and the mammalian target of rapamycin (mTOR). Importantly leptin (0.05, 0.10, 0.25 and 0.50 mu g/ml) significantly reduced the metabolic activity of PTCs, and significantly decreased protein content per cell. Investigation of the role of p44/42 and mTOR on metabolic activity and protein content per cell, demonstrated that in the presence of MAPK inhibitor U0126 and mTOR inhibitor Ku-63794, that the mTOR pathway is responsible for the reduction in PTC metabolic activity in response to leptin. However, p44/42 and mTOR play no role the reduced protein content per cell in OKs exposed to leptin. Therefore, leptin modulates metabolic activity in PTCs via an mTOR regulated pathway. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:38 / 45
页数:8
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