Overexpression of GPX2 gene regulates the development of porcine preadipocytes and skeletal muscle cells through MAPK signaling pathway

PLoS One. 2024 May 9;19(5):e0298827. doi: 10.1371/journal.pone.0298827. eCollection 2024.

Abstract

Glutathione peroxidase 2 (GPX2) is a selenium-dependent enzyme and protects cells against oxidative damage. Recently, GPX2 has been identified as a candidate gene for backfat and feed efficiency in pigs. However, it is unclear whether GPX2 regulates the development of porcine preadipocytes and skeletal muscle cells. In this study, adenoviral gene transfer was used to overexpress GPX2. Our findings suggest that overexpression of GPX2 gene inhibited proliferation of porcine preadipocytes. And the process is accompanied by the reduction of the p-p38. GPX2 inhibited adipogenic differentiation and promoted lipid degradation, while ERK1/2 was reduced and p-p38 was increased. Proliferation of porcine skeletal muscle cells was induced after GPX2 overexpression, was accompanied by activation in JNK, ERK1/2, and p-p38. Overexpression methods confirmed that GPX2 has a promoting function in myoblastic differentiation. ERK1/2 pathway was activated and p38 was suppressed during the process. This study lays a foundation for the functional study of GPX2 and provides theoretical support for promoting subcutaneous fat reduction and muscle growth.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes* / cytology
  • Adipocytes* / metabolism
  • Adipogenesis / genetics
  • Animals
  • Cell Differentiation / genetics
  • Cell Proliferation
  • Glutathione Peroxidase* / genetics
  • Glutathione Peroxidase* / metabolism
  • MAP Kinase Signaling System*
  • Muscle Fibers, Skeletal / cytology
  • Muscle Fibers, Skeletal / metabolism
  • Muscle, Skeletal / cytology
  • Muscle, Skeletal / metabolism
  • Swine
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Glutathione Peroxidase
  • p38 Mitogen-Activated Protein Kinases

Grants and funding

This study was supported by project funding provided by Tianjin Excellent Agricultural Science and Technology Special Commissioner and Support Projects to LP [23ZYCGSN00230], National Undergraduate Innovation and Entrepreneurship Training Program to LP [202310061006], Tianjin Key Laboratory of Green ecological feed to LP [TJ202302], Anhui Natural Science Foundation Project to GX and LP [2208085MC76], Key Research, the Tianjin Pig Industry Technology System Innovation Team, China to JZ [ITTPRS2024006], Key R&D and Transformation Program of Qinghai Province Science and Technology Assistance Program for Qinghai, China to GW [2023-NK-141], National Swine Industry Technology System to XL [CARS-35], and Agricultural Science and Technology Innovation Program to XL [ASTIP-IAS02].