Bovine Preadipocyte-Derived Exosomal miR-26a Promotes Intramuscular Adipogenesis by Directly Targeting <i>GSK3B</i>
Intramuscular fat (IMF) deposition is a critical determinant of beef quality, yet the regulatory role of preadipocyte-derived exosomes remains unclear. Exosomes (HC-Exo and CRSC-Exo) were isolated from preadipocytes of Haoyue Beef Cattle (HC) and Chinese Red Steppe Cattle (CRSC), breeds with distinct IMF contents. HC-Exo significantly enhanced preadipocyte proliferation and differentiation, increasing lipid droplet formation and triglyceride synthesis, alongside elevated expression levels of peroxisome proliferator-activated receptor γ (<i>PPAR</i>γ) and CCAAT enhancer binding protein alpha (<i>C/EBP</i>α). MiRNA sequencing identified 580 differentially expressed miRNAs, with miR-26a twice as abundant in HC-Exo versus CRSC-Exo. Integrated bioinformatics analyses, including KEGG, GO, and dual-luciferase reporter assays, identified glycogen synthase kinase-3B (<i>GSK3B</i>) as a direct target of miR-26a. Functional validation demonstrated that miR-26a mimics enhanced adipogenesis by suppressing <i>GSK3B</i> expression, while <i>GSK3B</i> overexpression inhibited differentiation. These findings establish exosomal miR-26a as a novel regulator of intramuscular adipogenesis, providing molecular insights for improving beef quality.
Authors
- Junfang Zhang
- Yiyang Du
- Lihong Qin
- Zijiao Zhao
- Yumin Zhao
- Yinghua Peng
- Jia Guo
Institutions
- Chinese Academy of Sciences (CN)
- Northeast Institute of Geography and Agroecology (CN)
- Jilin Academy of Agricultural Sciences (CN)
- Chinese Academy of Agricultural Sciences (CN)
- Ministry of Agriculture and Rural Affairs (CN)
- Institute of Special Animal and Plant Sciences (CN)
- National Beef Cattle Industrial Technology System (CN)
Publication Details
- Journal
- Journal of Agricultural and Food Chemistry
- Published
- 2026-02-25
- DOI
- https://doi.org/10.1021/acs.jafc.5c14739
- Primary Topic
- MicroRNA in disease regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00