Role of the energy sensor AMP-activated protein kinase in renal physiology and disease

被引:128
作者
Hallows, Kenneth R. [1 ,2 ]
Mount, Peter F. [3 ,4 ,5 ]
Pastor-Soler, Nuria M. [1 ,2 ]
Power, David A. [3 ,4 ,5 ]
机构
[1] Univ Pittsburgh, Dept Med, Renal Electrolyte Div, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Cell Biol & Physiol, Pittsburgh, PA USA
[3] Univ Melbourne, Dept Nephrol, Heidelberg, Vic, Australia
[4] Univ Melbourne, Dept Med, Heidelberg, Vic, Australia
[5] Austin Hlth, Kidney Lab, Heidelberg, Vic, Australia
基金
美国国家卫生研究院;
关键词
CFTR; ENaC; NKCC; adiponectin; FATTY-ACID OXIDATION; TRANSMEMBRANE CONDUCTANCE REGULATOR; EPITHELIAL NA+ CHANNEL; ACETYL-COA CARBOXYLASE; GLUCOSE-METABOLISM; MOLECULAR-CLONING; ADENOSINE-MONOPHOSPHATE; ENDOTHELIAL-CELLS; KEY REGULATOR; CL-SECRETION;
D O I
10.1152/ajprenal.00005.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Hallows KR, Mount PF, Pastor-Soler NM, Power DA. Role of the energy sensor AMP-activated protein kinase in renal physiology and disease. Am J Physiol Renal Physiol 298: F1067-F1077, 2010. First published February 24, 2010; doi:10.1152/ajprenal.00005.2010.-The ultrasensitive energy sensor AMP-activated protein kinase (AMPK) orchestrates the regulation of energy-generating and energy-consuming pathways. AMPK is highly expressed in the kidney where it is reported to be involved in a variety of physiological and pathological processes including ion transport, podocyte function, and diabetic renal hypertrophy. Sodium transport is the major energy-consuming process in the kidney, and AMPK has been proposed to contribute to the coupling of ion transport with cellular energy metabolism. Specifically, AMPK has been identified as a regulator of several ion transporters of significance in renal physiology, including the cystic fibrosis transmembrane conductance regulator (CFTR), the epithelial sodium channel (ENaC), the Na+-K+-2Cl(-) cotransporter (NKCC), and the vacuolar H+-ATPase (V-ATPase). Identified regulators of AMPK in the kidney include dietary salt, diabetes, adiponectin, and ischemia. Activation of AMPK in response to adiponectin is described in podocytes, where it reduces albuminuria, and in tubular cells, where it reduces glycogen accumulation. Reduced AMPK activity in the diabetic kidney is associated with renal accumulation of triglyceride and glycogen and the pathogenesis of diabetic renal hypertrophy. Acute renal ischemia causes a rapid and powerful activation of AMPK, but the functional significance of this observation remains unclear. Despite the recent advances, there remain significant gaps in the present understanding of both the upstream regulating pathways and the downstream substrates for AMPK in the kidney. A more complete understanding of the AMPK pathway in the kidney offers potential for improved therapies for several renal diseases including diabetic nephropathy, polycystic kidney disease, and ischemia-reperfusion injury.
引用
收藏
页码:F1067 / F1077
页数:11
相关论文
共 144 条
[1]   Intrasteric control of AMPK via the γ1 subunit AMP allosteric regulatory site [J].
Adams, J ;
Chen, ZP ;
Van Denderen, BJW ;
Morton, CJ ;
Parker, MW ;
Witters, LA ;
Stapleton, D ;
Kemp, BE .
PROTEIN SCIENCE, 2004, 13 (01) :155-165
[2]   AMPK controls epithelial Na+ channels through Nedd4-2 and causes an epithelial phenotype when mutated [J].
Almaca, Joana ;
Kongsuphol, Patthara ;
Hieke, Bernhard ;
Ousingsawat, Jiraporn ;
Viollet, Benoit ;
Schreiber, Rainer ;
Amaral, Margarida D. ;
Kunzelmann, Karl .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2009, 458 (04) :713-721
[3]  
ALZAMORA R, 2009, FASEB J, V23, P602
[4]   Components of a calmodulin-dependent protein kinase cascade -: Molecular cloning, functional characterization and cellular localization of Ca2+/calmodulin-dependent protein kinase kinase β [J].
Anderson, KA ;
Means, RL ;
Huang, QH ;
Kemp, BE ;
Goldstein, EG ;
Selbert, MA ;
Edelman, AM ;
Fremeau, RT ;
Means, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (48) :31880-31889
[5]   WNK1 and OSR1 regulate the Na+, K+, 2Cl- cotransporter in HeLa cells [J].
Anselmo, Anthony N. ;
Earnest, Svetlana ;
Chen, Wei ;
Juang, Yu-Chi ;
Kim, Sung Chan ;
Zhao, Yingming ;
Cobb, Melanie H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (29) :10883-10888
[6]   AMP-activated protein kinase in the heart - Role during health and disease [J].
Arad, Michael ;
Seidman, Christine E. ;
Seidman, J. G. .
CIRCULATION RESEARCH, 2007, 100 (04) :474-488
[7]   METABOLIC SUBSTRATE UTILIZATION BY RABBIT PROXIMAL TUBULE - AN NADH FLUORESCENCE STUDY [J].
BALABAN, RS ;
MANDEL, LJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (03) :F407-F416
[8]   Apoptosis of tubular epithelial cells in glycogen nephrosis during diabetes [J].
Bamri-Ezzine, S ;
Ao, ZJ ;
Londoño, I ;
Gingras, D ;
Bendayan, M .
LABORATORY INVESTIGATION, 2003, 83 (07) :1069-1080
[9]   Mechanisms of ENaC regulation and clinical implications [J].
Bhalla, Vivek ;
Hallows, Kenneth R. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2008, 19 (10) :1845-1854
[10]   AMP-activated kinase inhibits the epithelial Na+ channel through functional regulation of the ubiquitin ligase Nedd4-2 [J].
Bhalla, Vivek ;
Oyster, Nicholas M. ;
Fitch, Adam C. ;
Wijngaarden, Marjolein A. ;
Neumann, Dietbert ;
Schlattner, Uwe ;
Pearce, David ;
Hallows, Kenneth R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (36) :26159-26169