Published online before print April 20, 2009, doi: 10.1161/CIRCULATIONAHA.108.814145
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
(Circulation. 2009;119:2357-2366.)
© 2009 American Heart Association, Inc.
Molecular Cardiology |
MicroRNA-320 Is Involved in the Regulation of Cardiac Ischemia/Reperfusion Injury by Targeting Heat-Shock Protein 20
From the Departments of Pharmacology and Cell Biophysics (X.R., J.W., X.W., J.Q., K.J., P.N., T.J.P., G.F.) and Environmental Health (M.A.S.), University of Cincinnati College of Medicine, Cincinnati, Ohio. Present address of J.W. is Bassett Research Institute, Mary Imogene Bassett Hospital, Cooperstown, NY.
Correspondence to Guo-Chang Fan, PhD, Department of Pharmacology and Cell Biophysics, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267-0575. E-mail fangg{at}ucmail.uc.edu
Received August 11, 2008; accepted February 25, 2009.
Background— Recent studies have identified critical roles for microRNAs (miRNAs) in a variety of cellular processes, including regulation of cardiomyocyte death. However, the signature of miRNA expression and possible roles of miRNA in the ischemic heart have been less well studied.
Methods and Results— We performed miRNA arrays to detect the expression pattern of miRNAs in murine hearts subjected to ischemia/reperfusion (I/R) in vivo and ex vivo. Surprisingly, we found that only miR-320 expression was significantly decreased in the hearts on I/R in vivo and ex vivo. This was further confirmed by TaqMan real-time polymerase chain reaction. Gain-of-function and loss-of-function approaches were employed in cultured adult rat cardiomyocytes to investigate the functional roles of miR-320. Overexpression of miR-320 enhanced cardiomyocyte death and apoptosis, whereas knockdown was cytoprotective, on simulated I/R. Furthermore, transgenic mice with cardiac-specific overexpression of miR-320 revealed an increased extent of apoptosis and infarction size in the hearts on I/R in vivo and ex vivo relative to the wild-type controls. Conversely, in vivo treatment with antagomir-320 reduced infarction size relative to the administration of mutant antagomir-320 and saline controls. Using TargetScan software and proteomic analysis, we identified heat-shock protein 20 (Hsp20), a known cardioprotective protein, as an important candidate target for miR-320. This was validated experimentally by utilizing a luciferase/GFP reporter activity assay and examining the expression of Hsp20 on miR-320 overexpression and knockdown in cardiomyocytes.
Conclusions— Our data demonstrate that miR-320 is involved in the regulation of I/R-induced cardiac injury and dysfunction via antithetical regulation of Hsp20. Thus, miR-320 may constitute a new therapeutic target for ischemic heart diseases.
CLINICAL PERSPECTIVE
Related Article:
-
Clinical Summaries
Circulation 2009 119: 2295-2296.[Extract] [Full Text]
This article has been cited by other articles:
 |
|
 |
|
  W. K. Jones, G.-C. Fan, S. Liao, J.-M. Zhang, Y. Wang, N. L. Weintraub, E. G. Kranias, J. E. Schultz, J. Lorenz, and X. Ren Peripheral Nociception Associated With Surgical Incision Elicits Remote Nonischemic Cardioprotection Via Neurogenic Activation of Protein Kinase C Signaling Circulation, September 15, 2009; 120(11_suppl_1): S1 - S9. [Abstract] [Full Text] [PDF]
|
|