MicroRNA-33 promotes the replicative senescence of mouse embryonic fibroblasts by suppressing CDK6

Biochem Biophys Res Commun. 2016 May 13;473(4):1064-1070. doi: 10.1016/j.bbrc.2016.04.016. Epub 2016 Apr 6.

Abstract

MicroRNAs are a large class of tiny noncoding RNAs, which have emerged as critical regulators of gene expression, and thus are involved in multiple cellular processes, including cellular senescence. MicroRNA-33 has previously been established to exert crucial effect on cell proliferation, lipid metabolism and cholesterol metabolism. Nonetheless, the association between microRNA-33 and cellular senescence and its underlying molecular mechanism are far to be elucidated. The present study has attempted to probe into the effect of microRNA-33 on MEFs senescence. Our data unveiled that microRNA-33 was dramatically down-regulated in senescent MEFs compared to the young MEFs, and ectopic expression of microRNA-33 promoted MEFs senescence, while knock-down of microRNA-33 exhibited a protective effect against senescence phenotype. Moreover, we verified CDK6 as a direct target of microRNA-33 in mouse. Silencing of CDK6 induced the premature senescence phenotype of MEFs similarly as microRNA-33, while enforced expression of CDK6 significantly reverse the senescence-induction effect of microRNA-33. Taken together, our results suggested that microRNA-33 enhanced the replicative senescence of MEFs potentially by suppressing CDK6 expression.

Keywords: CDK6; Cellular senescence; MicroRNA-33; Proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation / physiology
  • Cells, Cultured
  • Cellular Senescence / physiology*
  • Cyclin-Dependent Kinase 6 / metabolism*
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / physiology*
  • Fibroblasts / cytology*
  • Fibroblasts / physiology*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • MicroRNAs / metabolism*

Substances

  • MicroRNAs
  • Mirn33 microRNA, mouse
  • Cdk6 protein, mouse
  • Cyclin-Dependent Kinase 6