miR-128-3p regulates chicken granulosa cell function via 14-3-3β/FoxO and PPAR-γ/LPL signaling pathways

Int J Biol Macromol. 2023 Jun 30:241:124654. doi: 10.1016/j.ijbiomac.2023.124654. Epub 2023 Apr 27.

Abstract

MicroRNAs (miRNAs) are class of 22 nt short RNA sequences which inhibit protein translation through binding to the 3'UTR of its target genes. The continuous ovulatory property of chicken follicle makes it a perfect model for studying granulosa cell (GC) functions. In this study, we found that large number of miRNAs including miR-128-3p, were differentially expressed in the GCs of F1 and F5 follicles of chicken. Subsequently, the results revealed that miR-128-3p inhibited proliferation, the formation of lipid droplets, and hormone secretion in chicken primary GCs through directly targeting YWHAB and PPAR-γ genes. To determine the effects of 14-3-3β (encoded by YWHAB) protein on GCs functions, we overexpressed or inhibited the expression of YWHAB, and the results showed that YWHAB inhibited the function of FoxO proteins. Collectively, we found that miR-128-3p was highly expressed in the chicken F1 follicles compared to the F5 follicles. In addition, the results indicated that miR-128-3p promoted GC apoptosis through 14-3-3β/FoxO pathway via repressing YWHAB, and inhibited lipid synthesis by impeding the PPAR-γ/LPL pathway, as well as reduced the secretion of progesterone and estrogen. Taken together, the results showed that miR-128-3p plays a regulatory role in chicken granulosa cell function via 14-3-3β/FoxO and PPAR-γ/LPL signaling pathways.

Keywords: 14-3-3β/FoxO pathway; Chicken granulosa cell; Lipid droplet; PPAR-γ/LPL pathway; miR-128-3p.

MeSH terms

  • Animals
  • Cell Proliferation / genetics
  • Chickens* / metabolism
  • Female
  • Granulosa Cells / metabolism
  • MicroRNAs* / genetics
  • MicroRNAs* / metabolism
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • Peroxisome Proliferator-Activated Receptors / pharmacology
  • Signal Transduction

Substances

  • Peroxisome Proliferator-Activated Receptors
  • MicroRNAs