4.6 Article

Upregulated expression of miR-1/miR-206 in a rat model of myocardial infarction

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2009.02.097

Keywords

MicroRNAs; Ischemia; Myocardial infarction; Gene expression; IGF-1; Apoptosis; Serum deprivation; Hypoxia

Funding

  1. National Natural Science Foundation of China [30672077, 30772142]
  2. National Key Basic Research Program (NKBRP) of China [2006CB503806]

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MicroRNAs (miRNAs) have been increasingly reported to have important roles in diverse biological and pathological processes. We investigated miR-1 and miR-206 expression and their potential roles in a rat model of myocardial infarction (MI). miR-1 and miR-206 expression were significantly increased, and insulin-like growth factor 1 (IGF-1) protein was markedly reduced without obvious change of its mRNA level after MI induction. Position 175-196 of rat IGF-1 3'-untranslated region was identified to be required for efficient downregulation by miR-1/miR-206. IGF-1 level was reduced without changing its transcript level in rat H9C2 myoblast cells modified with miR-1 (H9C2-miR-1). In the serum withdrawal and hypoxic condition, caspase-3 activity and mitochondrial potential were significantly increased in H9C2-miR-1 cells compared with the control group, respectively (p < 0.05, p < 0.01). Together, our results indicate that miR-1 and miR-206 are involved in apoptotic cell death in MI by post-transcriptional repression of IGF-1. (C) 2009 Elsevier Inc. All rights reserved.

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