Pigment Epithelium-Derived Factor Regulates Lipid Metabolism via Adipose Triglyceride Lipase

被引:117
作者
Borg, Melissa L. [1 ]
Andrews, Zane B. [1 ]
Duh, Ella J. [2 ]
Zechner, Rudolf [3 ]
Meikle, Peter J. [4 ]
Watt, Matthew J. [1 ]
机构
[1] Monash Univ, Dept Physiol, Biol Lipid Metab Lab, Clayton, Vic 3168, Australia
[2] Johns Hopkins Univ, Sch Med, Wilmer Ophthalmol Inst, Baltimore, MD 21205 USA
[3] Karl Franzens Univ Graz, Inst Mol Biosci, Graz, Austria
[4] Baker IDI Heart & Diabet Inst, Metabol Lab, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
HORMONE-SENSITIVE LIPASE; HUMAN SKELETAL-MUSCLE; FATTY-ACID OXIDATION; TRIACYLGLYCEROL LIPASE; INSULIN-RESISTANCE; ENERGY-METABOLISM; IDENTIFICATION; OBESITY; TISSUE; EXPRESSION;
D O I
10.2337/db10-0845
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Pigment epithelium-derived factor (PEDF) is an adipocyte-secreted factor involved in the development of insulin resistance in obesity. Previous studies have identified PEDF as a regulator of triacylglycerol metabolism in the liver that may act through adipose triglyceride lipase (ATGL). We used ATGL(-/-) mice to determine the role of PEDF in regulating lipid and glucose metabolism. RESEARCH DESIGN AND METHODS Recombinant PEDF was administered to ATGL(-/-) and wild-type mice, and whole-body energy metabolism was studied by indirect calorimety. Adipose tissue lipolysis and skeletal muscle fatty acid metabolism was determined in isolated tissue preparations. Muscle lipids were assessed by electrospray ionization-tandem mass spectrometry. Whole-body insulin sensitivity and skeletal muscle glucose uptake were assessed. RESULTS PEDF-impaired the capacity to adjust substrate selection, resulting in a delayed diurnal decline in the respiratory exchange ratio, and suppressed daily fatty acid oxidation. PEDF enhanced adipocyte lipolysis and triacylglycerol lipase activity in skeletal muscle. Muscle fatty acid uptake and storage were unaffected, whereas fatty acid oxidation was impaired. These changes in lipid metabolism were abrogated in ATGL(-/-) mice and were not attributable to hypothalamic actions. ATGL(-/-) mice were also refractory to PEDF-mediated insulin resistance, but this was not related to changes in lipid species in skeletal muscle. CONCLUSIONS-The results are the first direct demonstration that 1) PEDF influences systemic fatty acid metabolism by promoting lipolysis in an ATGL-dependent manner and reducing fatty acid oxidation and 2) ATGL is required for the negative effects of PEDF on insulin action. Diabetes 60:1458-1466, 2011
引用
收藏
页码:1458 / 1466
页数:9
相关论文
共 52 条
[1]   Adipose Overexpression of Desnutrin Promotes Fatty Acid Use and Attenuates Diet-Induced Obesity [J].
Ahmadian, Maryam ;
Duncan, Robin E. ;
Varady, Krista A. ;
Frasson, Danubia ;
Hellerstein, Marc K. ;
Birkenfeld, Andreas L. ;
Samuel, Varman T. ;
Shulman, Gerald I. ;
Wang, Yuhui ;
Kang, Chulho ;
Sul, Hei Sook .
DIABETES, 2009, 58 (04) :855-866
[2]   Characterization of the human visceral adipose tissue secretome [J].
Alvarez-Llamas, Gloria ;
Szalowska, Ewa ;
de Vries, Marcel P. ;
Weening, Desiree ;
Landman, Karloes ;
Hoek, Annemieke ;
Wolffenbuttel, Bruce H. R. ;
Roelofsen, Han ;
Vonk, Roel J. .
MOLECULAR & CELLULAR PROTEOMICS, 2007, 6 (04) :589-600
[3]   Dynamic activity of lipid droplets: Protein phosphorylation and GTP-Mediated protein translocation [J].
Bartzt, Rene ;
Zehmer, John K. ;
Zhu, Meifang ;
Chen, Yue ;
Serrero, Ginette ;
Zhao, Yingming ;
Liu, Pingsheng .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (08) :3256-3265
[4]  
Bilak MM, 2002, J NEUROSCI, V22, P9378
[5]   Endurance training in obese humans improves glucose tolerance and mitochondrial fatty acid oxidation and alters muscle lipid content [J].
Bruce, Clinton R. ;
Thrush, A. Brianne ;
Mertz, Valerie A. ;
Bezaire, Veronic ;
Chabowski, Adrian ;
Heigenhauser, George J. F. ;
Dyck, David J. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2006, 291 (01) :E99-E107
[6]   Overexpression of Carnitine Palmitoyltransferase-1 in Skeletal Muscle Is Sufficient to Enhance Fatty Acid Oxidation and Improve High-Fat Diet-Induced Insulin Resistance [J].
Bruce, Clinton R. ;
Hoy, Andrew J. ;
Turner, Nigel ;
Watt, Matthew J. ;
Allen, Tamara L. ;
Carpenter, Kevin ;
Cooney, Gregory J. ;
Febbraio, Mark A. ;
Kraegen, Edward W. .
DIABETES, 2009, 58 (03) :550-558
[7]   Identification of a lipokine, a lipid hormone linking adipose tissue to systemic metabolism [J].
Cao, Haiming ;
Gerhold, Kristin ;
Mayers, Jared R. ;
Wiest, Michelle M. ;
Watkins, Steven M. ;
Hotamisligil, Goekhan S. .
CELL, 2008, 134 (06) :933-944
[8]   Continuous fat oxidation in acetyl-CoA carboxylase 2 knockout mice increases total energy expenditure, reduces fat mass, and improves insulin sensitivity [J].
Choi, Cheol Soo ;
Savage, David B. ;
Abu-Elheiga, Lutfi ;
Liu, Zhen-Xiang ;
Kim, Sheene ;
Kulkarni, Ameya ;
Distefano, Alberto ;
Hwang, Yu-Jin ;
Reznick, Richard M. ;
Codella, Roberto ;
Zhang, Dongyan ;
Cline, Gary W. ;
Wakil, Salih J. ;
Shulman, Gerald I. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (42) :16480-16485
[9]   Anti-angiogenic pigment epithelium-derived factor regulates hepatocyte triglyceride content through adipose triglyceride lipase (ATGL) [J].
Chung, Chuhan ;
Doll, Jennifer A. ;
Gattu, Arijeet K. ;
Shugrue, Christine ;
Cornwell, Mona ;
Fitchev, Philip ;
Crawford, Susan E. .
JOURNAL OF HEPATOLOGY, 2008, 48 (03) :471-478
[10]   Pigment Epithelium-Derived Factor Contributes to Insulin Resistance in Obesity [J].
Crowe, Seamus ;
Wu, Lindsay E. ;
Economou, Catherine ;
Turpin, Sarah M. ;
Matzaris, Maria ;
Hoehn, Kyle L. ;
Hevener, Andrea L. ;
James, David E. ;
Duh, Elia J. ;
Watt, Matthew J. .
CELL METABOLISM, 2009, 10 (01) :40-47