miR-33a Inhibits the Differentiation of Bovine Preadipocytes through the IRS2-Akt Pathway

Genes (Basel). 2023 Feb 20;14(2):529. doi: 10.3390/genes14020529.

Abstract

Several microRNAs (miRNAs) are known to participate in adipogenesis. However, their role in this process, especially in the differentiation of bovine preadipocytes, remains to be elucidated. This study was intended to clarify the effect of microRNA-33a (miR-33a) on the differentiation of bovine preadipocytes by cell culture, real-time fluorescent quantitative PCR (qPCR), Oil Red staining, BODIPY staining, and Western blotting. The results indicate that overexpression of miR-33a significantly inhibited lipid droplet accumulation and decreased the mRNA and protein expression of adipocyte differentiation marker genes such as peroxisome proliferator-activated receptor gamma (PPARγ), sterol regulatory element-binding protein 1 (SREBP1), and fatty acid-binding protein 4 (FABP4). In contrast, the interference expression of miR-33a promoted lipid droplet accumulation and increased the expression of marker genes. Additionally, miR-33a directly targeted insulin receptor substrate 2 (IRS2) and regulated the phosphorylation level of serine/threonine kinase (Akt). Furthermore, miR-33a inhibition could rescue defects in the differentiation of bovine preadipocytes and the Akt phosphorylation level caused by small interfering IRS2 (si-IRS2). Collectively, these results indicate that miR-33a could inhibit the differentiation of bovine preadipocytes, possibly through the IRS2-Akt pathway. These findings might help develop practical means to improve the quality of beef.

Keywords: Akt pathway; IRS2; bovine; miR-33a; preadipocyte differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis / genetics
  • Animals
  • Cattle
  • Cell Differentiation
  • Insulin Receptor Substrate Proteins
  • MicroRNAs* / genetics
  • Proto-Oncogene Proteins c-akt* / metabolism

Substances

  • Proto-Oncogene Proteins c-akt
  • Insulin Receptor Substrate Proteins
  • MicroRNAs

Grants and funding

This study was funded by the National Natural Science Foundation of China (31972994), Shaanxi Livestock and Poultry Breeding Double-chain Fusion Key Project (2022GD-TSLD-46-0102), Special Project for the Central Government to Guide Local Science and Technology Development (2060404-51301) the National Beef and Yak Industrial Technology System (CARS-37), and the Key Research and Development Program of Shaanxi Province (2022NY-050, 2022ZDLNY01-01).