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Integrated microRNA and mRNA responses to acute human left ventricular ischemia
Author(s) -
Louis Saddic,
Tzuu-Wang Chang,
Martin I. Sigurðsson,
Mahyar Heydarpour,
Benjamin A. Raby,
Stanton K. Shernan,
Sary F. Aranki,
Simon C. Body,
Jochen D. Muehlschlegel
Publication year - 2015
Publication title -
physiological genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.078
H-Index - 112
eISSN - 1531-2267
pISSN - 1094-8341
DOI - 10.1152/physiolgenomics.00049.2015
Subject(s) - microrna , biology , ischemia , messenger rna , cardiopulmonary bypass , gene expression , downregulation and upregulation , aortic cross clamp , medicine , bioinformatics , gene , genetics
MicroRNAs (miRNAs) play a significant role in ischemic heart disease. Animal models of left ventricular (LV) ischemia demonstrate a unique miRNA profile; however, these models have limitations in describing human disease. In this study, we performed next-generation miRNA and mRNA sequencing on LV tissue from nine patients undergoing cardiac surgery with cardiopulmonary bypass and cardioplegic arrest. Samples were obtained immediately after aortic cross clamping (baseline) and before aortic cross clamp removal (postischemic). Of 1,237 identified miRNAs, 21 were differentially expressed between baseline and postischemic LV samples including the upregulated miRNAs miR-339-5p and miR-483-3p and the downregulated miRNA miR-139-5p. Target prediction analysis of these miRNAs was integrated with mRNA expression from the same LV samples to identify anticorrelated miRNA-mRNA pairs. Gene enrichment studies of candidate mRNA targets demonstrated an association with cardiovascular disease, cell death, and metabolism. Therapeutics that intervene on these miRNAs and their downstream targets may lead to novel mechanisms of mitigating the damage caused by ischemic insults on the human heart.

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