FEBS Letters · 2014 · 95 citations · 35 references
Life SciencesCell BiologyMolecular BiologyApoptosisGene ExpressionTranscriptional RegulationApoptosis RegulationCellular Responses To HypoxiaHypoxia AdaptationIschemic Heart DiseaseMicrorna BiologyMicrorna-mediated RegulationHif-1 Alpha RegulationHypoxia ModulationHypoxia-inducible Factor RegulationHypoxia-inducible Factor SignalingMicrorna Regulation Of ApoptosisMicrorna-mediated Apoptosis ControlMyocardial Ischemia MarkersTherapeutic Target Identification
Accumulating evidence suggests that hypoxia-inducible factor 1α (HIF-1α) regulates numerous miRNAs and is crucial for cellular response to hypoxia. However, the relationship between HIF-1α and miR-21 in hypoxic cardiomyocytes is little known. We found that hypoxia induced HIF-1α and miR-21 expression. HIF-1α knockdown increased cell apoptosis and reduced miR-21 expression. Furthermore, we found that HIF-1α transcriptionally enhanced miR-21 promoter activity by binding to its promoter, which required the recruitment of CBP/p300. In addition, we found that miR-21 inhibition increased cell apoptosis and reduced HIF-1α expression, and modulated the PTEN/Akt pathway. Our results indicate that HIF-1α-miR-21 feedback contributes to the adaptation of cardiomyocytes to hypoxia, and has potential as therapeutic target for myocardial ischemia.
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