Investigation of Mitochondrial Adaptations to Modulation of Carbohydrate Supply during Adipogenesis of 3T3-L1 Cells by Targeted 1H-NMR Spectroscopy

Biomolecules. 2021 Apr 29;11(5):662. doi: 10.3390/biom11050662.

Abstract

(1) Background: White adipose tissue (WAT) is a dynamic and plastic tissue showing high sensitivity to carbohydrate supply. In such a context, the WAT may accordingly modulate its mitochondrial metabolic activity. We previously demonstrated that a partial replacement of glucose by galactose in a culture medium of 3T3-L1 cells leads to a poorer adipogenic yield and improved global mitochondrial health. In the present study, we investigate key mitochondrial metabolic actors reflecting mitochondrial adaptation in response to different carbohydrate supplies. (2) Methods: The metabolome of 3T3-L1 cells was investigated during the differentiation process using different glucose/galactose ratios and by a targeted approach using 1H-NMR (Proton nuclear magnetic resonance) spectroscopy; (3) Results: Our findings indicate a reduction of adipogenic and metabolic overload markers under the low glucose/galactose condition. In addition, a remodeling of the mitochondrial function triggers the secretion of metabolites with signaling and systemic energetical homeostasis functions. Finally, this study also sheds light on a new way to consider the mitochondrial metabolic function by considering noncarbohydrates related pathways reflecting both healthier cellular and mitochondrial adaptation mechanisms; (4) Conclusions: Different carbohydrates supplies induce deep mitochondrial metabolic and function adaptations leading to overall adipocytes function and profile remodeling during the adipogenesis.

Keywords: adaptation; adipogenesis; carbohydrates; metabolism; metabolomics; mitochondria.

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis*
  • Animals
  • Carbohydrate Metabolism
  • Cell Culture Techniques
  • Cell Differentiation
  • Culture Media / chemistry*
  • Galactose / chemistry
  • Glucose / chemistry
  • Metabolomics / methods*
  • Mice
  • Mitochondria / metabolism*
  • Proton Magnetic Resonance Spectroscopy

Substances

  • Culture Media
  • Glucose
  • Galactose