miR-1285-3p targets TPI1 to regulate the glycolysis metabolism signaling pathway of Tibetan sheep Sertoli cells

PLoS One. 2022 Sep 22;17(9):e0270364. doi: 10.1371/journal.pone.0270364. eCollection 2022.

Abstract

Glycolysis in Sertoli cells (SCs) can provide energy substrates for the development of spermatogenic cells. Triose phosphate isomerase 1 (TPI1) is one of the key catalytic enzymes involved in glycolysis. However, the biological function of TPI1 in SCs and its role in glycolytic metabolic pathways are poorly understood. On the basis of a previous research, we isolated primary SCs from Tibetan sheep, and overexpressed TPI1 gene to determine its effect on the proliferation, glycolysis, and apoptosis of SCs. Secondly, we investigated the relationship between TPI1 and miR-1285-3p, and whether miR-1285-3p regulates the proliferation and apoptosis of SCs, and participates in glycolysis by targeting TPI1. Results showed that overexpression of TPI1 increased the proliferation rate and decreased apoptosis of SCs. In addition, overexpression of TPI1 altered glycolysis and metabolism signaling pathways and significantly increased amount of the final product lactic acid. Further analysis showed that miR-1285-3p inhibited TPI1 by directly targeting its 3'untranslated region. Overexpression of miR-1285-3p suppressed the proliferation of SCs, and this effect was partially reversed by restoration of TPI1 expression. In summary, this study shows that the miR-1285-3p/TPI1 axis regulates glycolysis in SCs. These findings add to our understanding on the regulation of spermatogenesis in sheep and other mammals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Proliferation
  • Glycolysis / genetics
  • Lactic Acid / metabolism
  • Male
  • Mammals / genetics
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Sertoli Cells* / metabolism
  • Sheep / genetics
  • Signal Transduction
  • Tibet
  • Triose-Phosphate Isomerase / genetics
  • Untranslated Regions

Substances

  • MicroRNAs
  • Untranslated Regions
  • Lactic Acid
  • Triose-Phosphate Isomerase

Associated data

  • Dryad/10.5061/dryad.5dv41ns7k

Grants and funding

The study was supported by the Education science and technology innovation project of Gansu Province (GSSYLXM-02), National Natural Science Foundation of China (31960662), National Key R&D Program of China (2021YFD1100502) and "Innovation Star" project for outstanding graduate students of the Education Department of Gansu Province (2021CXZX-350). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.