MiR-141-3p regulates proliferation and senescence of stem cells from apical papilla by targeting YAP

Exp Cell Res. 2019 Oct 15;383(2):111562. doi: 10.1016/j.yexcr.2019.111562. Epub 2019 Aug 19.

Abstract

Biological phenotypes of mesenchymal stem cells (MSCs) are regulated by a series of biochemical elements, including microRNAs, hormones and growth factors. Our previous study illustrated a significant role of miR-141-3p during the osteogenic differentiation of stem cells from apical papilla (SCAPs). Nevertheless, the functions of miR-141-3p in regulating the proliferative ability and senescence of SCAPs have not been determined. This study identified that overexpression of miR-141-3p inhibited the proliferative ability of SCAPs. Meanwhile, the senescence of SCAPs was ahead of time. Conversely, transfection of miR-141-3p inhibitor promoted the proliferative ability of SCAPs and delayed their senescence. Yes-associated protein (YAP) was predicted as the downstream target gene of miR-141-3p by online softwares (miRDB, miRTarBase, miRWalk, and TargetScan), and was further verified by dual-luciferase reporter gene assay. Additionally, knockdown of YAP inhibited the proliferation and accelerated the senescence of SCAPs. Collectively, these findings proposed a novel direction that miR-141-3p impeded proliferative ability and promoted senescence of SCAPs through post-transcriptionally downregulating YAP.

Keywords: Proliferation; Senescence; Stem cells; YAP; miR-141-3p.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Cell Cycle Proteins / genetics*
  • Cell Differentiation / genetics
  • Cell Proliferation / genetics*
  • Cells, Cultured
  • Cellular Senescence / genetics*
  • Dental Papilla / metabolism*
  • Gene Expression Regulation
  • HEK293 Cells
  • Humans
  • Mesenchymal Stem Cells / metabolism*
  • MicroRNAs / physiology*
  • Osteogenesis / genetics
  • Periapical Tissue / cytology
  • Periapical Tissue / metabolism
  • Transcription Factors / genetics*
  • Young Adult

Substances

  • Cell Cycle Proteins
  • MIRN141 microRNA, human
  • MicroRNAs
  • Transcription Factors
  • YY1AP1 protein, human