miR-34c works downstream of p53 leading to dairy goat male germline stem-cell (mGSCs) apoptosis

Cell Prolif. 2013 Apr;46(2):223-31. doi: 10.1111/cpr.12013.

Abstract

Objectives: Recent lines of evidence have indicated that miR-34c can play important roles in regulation of the cell cycle, cell senescence and apoptosis of mouse and human tumour cells, spermatogenesis, and male germ-cell apoptosis. However, there is little information on the effects of miR-34c on proliferation and apoptosis of livestock male germ cells. The dairy goat is a convenient domestic species for biological investigation and application. The purpose of this study was to investigate the effects of miR-34c on apoptosis and proliferation of dairy goat male germline stem cells (mGSCs), as well as to determine the relationship between p53 and miR-34c in this species.

Materials and methods: Morphological observation, miRNA in situ hybridisation (ISH), bromodeoxyuridine staining, flow cytometry, quantitative-RT-PCR (Q-RT-PCR) and western blotting were utilized to ascertain apoptosis and proliferation of mGSCs, through transfection of miR-34c mimics (miR-34c), miR-34c inhibitor (anti-miR-34c), miR-34c mimics and inhibitors co-transfected (mixture) compared to control groups.

Results: Results manifested that miR-34c over-expression promoted mGSCs apoptosis and suppressed their proliferation. Simultaneously, a variety of apoptosis-related gene expression was increased while some proliferation-related genes were downregulated. Accordingly, miR-34c promoted apoptosis in mGSCs and reduced their proliferation; moreover, expression of miR-34c was p53-dependent.

Conclusions: This study is the first to provide a model for study of miRNAs and mechanisms of proliferation and apoptosis in male dairy goat germ cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Blotting, Western
  • Bromodeoxyuridine / metabolism
  • Cell Proliferation
  • Dose-Response Relationship, Drug
  • Doxorubicin / pharmacology
  • Flow Cytometry
  • Gene Expression Regulation, Neoplastic
  • Goats / growth & development
  • Goats / metabolism*
  • In Situ Hybridization
  • Male
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / genetics
  • MicroRNAs / metabolism*
  • Real-Time Polymerase Chain Reaction / methods
  • Spermatozoa / metabolism
  • Spermatozoa / pathology
  • Stem Cells / metabolism
  • Stem Cells / pathology*
  • Testis / metabolism
  • Testis / pathology
  • Time Factors
  • Transcriptional Activation
  • Transfection
  • Tumor Suppressor Protein p53 / genetics
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • MicroRNAs
  • Tumor Suppressor Protein p53
  • Doxorubicin
  • Bromodeoxyuridine