Phenotypic characteristics of adipocyte-like cells generated from C2C12 myoblasts cultured with chicken serum

Biochem Biophys Res Commun. 2024 Dec 3:736:150843. doi: 10.1016/j.bbrc.2024.150843. Epub 2024 Oct 16.

Abstract

The aim of this study was to clarify the transcriptional and metabolic characteristics of C2C12 myoblasts cultured in Dulbecco's Modified Eagle Medium (DMEM) containing 20 % chicken serum (CHS) (C2C12-CHS cells) compared with C2C12 myoblasts cultured in DMEM containing 20 % fetal bovine serum (FBS) (C2C12-FBS cells). After 3 days of culture, C2C12-CHS cells showed a marked accumulation of lipid droplets, accompanied by increased expression levels of brown adipocyte-related genes (i.e., Bmp7, Prdm16, Ucp1, Cidea, Pgc1α, Cox7a1, Cox8, and β3-adorenoceptor). Furthermore, stimulation of β3-adorenoceptor by its selective agonist, mirabegron, increased the mRNA expression of Ucp1 and Pgc1α in C2C12-CHS cells. Wide-targeted metabolomic analysis performed by gas chromatography-tandem mass spectrometry revealed that the metabolic profile of C2C12-CHS cells was obviously different to that of C2C12-FBS cells. Additionally, the metabolomic analysis indicated that β3-adrenoceptor stimulation by mirabegron upregulated energy metabolism in C2C12-CHS cells as seen in brown adipocytes. These results suggest that C2C12-CHS cells may differentiate into brown adipocyte-like cells, accompanied by increased functional β3-adrenoceptor.

Keywords: Brown adipocyte; Chicken serum; Metabolites; Metabolomics; Myoblast.

MeSH terms

  • Acetanilides / pharmacology
  • Adipocytes / cytology
  • Adipocytes / metabolism
  • Adipocytes, Brown / cytology
  • Adipocytes, Brown / metabolism
  • Adrenergic beta-3 Receptor Agonists / pharmacology
  • Animals
  • Apoptosis Regulatory Proteins
  • Cell Differentiation
  • Cell Line
  • Chickens*
  • Culture Media / pharmacology
  • DNA-Binding Proteins
  • Energy Metabolism
  • Mice
  • Myoblasts* / cytology
  • Myoblasts* / metabolism
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / genetics
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha / metabolism
  • Phenotype
  • Receptors, Adrenergic, beta-3 / genetics
  • Receptors, Adrenergic, beta-3 / metabolism
  • Serum / metabolism
  • Thiazoles* / pharmacology
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism

Substances

  • Thiazoles
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Acetanilides
  • mirabegron
  • Ucp1 protein, mouse
  • Ppargc1a protein, mouse
  • Uncoupling Protein 1
  • Receptors, Adrenergic, beta-3
  • Transcription Factors
  • Adrenergic beta-3 Receptor Agonists
  • Cidea protein, mouse
  • Prdm16 protein, mouse
  • Adrb3 protein, mouse
  • Culture Media
  • DNA-Binding Proteins
  • Apoptosis Regulatory Proteins