Subcellular trafficking of the substrate transporters GLUT4 and CD36 in cardiomyocytes

被引:73
作者
Steinbusch, Laura K. M. [1 ]
Schwenk, Robert W. [1 ]
Ouwens, D. Margriet [2 ]
Diamant, Michaela [3 ]
Glatz, Jan F. C. [1 ]
Luiken, Joost J. F. P. [1 ]
机构
[1] Maastricht Univ, Dept Mol Genet, Cardiovasc Res Inst Maastricht, NL-6200 MD Maastricht, Netherlands
[2] German Diabet Ctr, Inst Clin Biochem & Pathobiochem, Dusseldorf, Germany
[3] Vrije Univ Amsterdam Med Ctr, Dept Endocrinol, Ctr Diabet, Amsterdam, Netherlands
关键词
Cardiac metabolism; Intracellular traffic; GLUT4; CD36; Insulin resistance; Diabetes; ACTIVATED PROTEIN-KINASE; FATTY-ACID UPTAKE; RESPONSIVE GLUCOSE-TRANSPORTER; SKELETAL-MUSCLE; PLASMA-MEMBRANE; INSULIN-RESISTANCE; CORTICAL ACTIN; BREFELDIN-A; DIABETIC CARDIOMYOPATHY; CARDIOVASCULAR-DISEASE;
D O I
10.1007/s00018-011-0690-x
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
Cardiomyocytes use glucose as well as fatty acids for ATP production. These substrates are transported into the cell by glucose transporter 4 (GLUT4) and the fatty acid transporter CD36. Besides being located at the sarcolemma, GLUT4 and CD36 are stored in intracellular compartments. Raised plasma insulin concentrations and increased cardiac work will stimulate GLUT4 as well as CD36 to translocate to the sarcolemma. As so far studied, signaling pathways that regulate GLUT4 translocation similarly affect CD36 translocation. During the development of insulin resistance and type 2 diabetes, CD36 becomes permanently localized at the sarcolemma, whereas GLUT4 internalizes. This juxtaposed positioning of GLUT4 and CD36 is important for aberrant substrate uptake in the diabetic heart: chronically increased fatty acid uptake at the expense of glucose. To explain the differences in subcellular localization of GLUT4 and CD36 in type 2 diabetes, recent research has focused on the role of proteins involved in trafficking of cargo between subcellular compartments. Several of these proteins appear to be similarly involved in both GLUT4 and CD36 translocation. Others, however, have different roles in either GLUT4 or CD36 translocation. These trafficking components, which are differently involved in GLUT4 or CD36 translocation, may be considered novel targets for the development of therapies to restore the imbalanced substrate utilization that occurs in obesity, insulin resistance and diabetic cardiomyopathy.
引用
收藏
页码:2525 / 2538
页数:14
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