Adipocyte Fatty Acid-Binding Protein Suppresses Cardiomyocyte Contraction A New Link Between Obesity and Heart Disease

被引:171
作者
Lamounier-Zepter, Valeria [1 ]
Look, Christiane [1 ]
Alvarez, Julio [2 ]
Christ, Torsten [3 ]
Ravens, Ursula [3 ]
Schunck, Wolf-Hagen [4 ]
Ehrhart-Bornstein, Monika [1 ]
Bornstein, Stefan R. [1 ]
Morano, Ingo [4 ,5 ]
机构
[1] Tech Univ Dresden, Med Clin 3, D-01307 Dresden, Germany
[2] Inst Cardiol, Havana, Cuba
[3] Tech Univ Dresden, Dept Pharmacol & Toxicol, D-01307 Dresden, Germany
[4] Max Delbruck Ctr Mol Med, Berlin, Germany
[5] Charite, D-13353 Berlin, Germany
关键词
FABP4; heart failure; adipocytes; metabolic syndrome; EPICARDIAL ADIPOSE-TISSUE; METABOLIC SYNDROME; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; APOLIPOPROTEIN-E; AP2; ATHEROSCLEROSIS; FAILURE; RISK; MICE;
D O I
10.1161/CIRCRESAHA.109.200501
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: Adipocyte fatty acid-binding protein (FABP4) is a member of the intracellular lipid-binding protein family and is predominantly expressed in adipose tissue. Emerging evidence suggests that FABP4 plays a role in some aspects of the metabolic syndrome including the development of type 2 diabetes and atherosclerosis. We have recently reported that secretory products from human adipocytes directly and acutely depressed cardiac contractile function. Objective: The purpose of this study was to identify this adipocyte-derived cardiodepressant factor. Methods and Results: Through mass spectrometry and immunoblotting, we have identified this cardiodepressant factor as FABP4. FABP4 represents 1.8% to 8.1% of total protein secreted by adipocytes in extracellular medium. FABP4 acutely depressed shortening amplitude as well as intracellular systolic peak Ca(2+) in a dose-dependent manner in isolated rat cardiomyocytes. Heart-specific FABP isoform (FABP3) revealed a similar cardiodepressant effect. The N-terminal amino acids 1 to 20 of FABP4 could be identified as the most effective cardiodepressive domain. We could exclude any effect of FABP4 on action potential duration and L-type Ca(2+) current, suggesting a reduced excitation-contraction gain caused by FABP4 as the main inhibitory mechanism. Conclusion: We conclude that the release of FABP4 from adipocytes may be involved in the development of cardiac contractile dysfunction of obese subjects. (Circ Res. 2009; 105: 326-334.)
引用
收藏
页码:326 / U34
页数:10
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