Self-assembled hyaluronic acid nanoparticle suppresses fat accumulation via CD44 in diet-induced obese mice

Carbohydr Polym. 2020 Jun 1:237:116161. doi: 10.1016/j.carbpol.2020.116161. Epub 2020 Mar 18.

Abstract

Obesity, a major risk factor for type 2 diabetes and cardiovascular diseases, is characterized by an abnormal expansion of adipose tissue. Herein, we investigated the potential of hyaluronic acid nanoparticles (HA-NPs) as therapeutics to treat obesity-related diseases by assessing the in vitro and in vivo effects of HA-NPs on adipogenesis and lipogenesis. Treatment of 3T3-L1 preadipocytes with HA-NPs resulted in a dose-dependent suppression of adipogenesis and lipid accumulation, and decreased the expression of key adipogenic and lipogenic regulators. However, these HA-NPs mediated effects were not observed in 3T3-L1 cells transfected with siRNAs against CD44, a major HA receptor. Further, HA-NP treatment of diet-induced obese (DIO) mice reduced the epididymal fat mass and suppressed the induction of adipogenic and lipogenic regulators, while these effects were attenuated in the CD44-null mice. Thus, our study provides a better understanding of how HA-NP modulates fat accumulation and presents a potential anti-obesity strategy targeting CD44.

Keywords: Adipogenesis; Hyaluronic acid; Lipogenesis; Obesity; Self-assembled nanoparticles.

MeSH terms

  • 3T3-L1 Cells
  • Adipogenesis / drug effects*
  • Animals
  • Diet, High-Fat
  • Hyaluronan Receptors / genetics*
  • Hyaluronic Acid / administration & dosage*
  • Hyaluronic Acid / chemistry
  • Lipogenesis / drug effects*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nanoparticles / administration & dosage*
  • Nanoparticles / chemistry
  • Obesity / drug therapy*
  • Obesity / genetics
  • Obesity / metabolism

Substances

  • Cd44 protein, mouse
  • Hyaluronan Receptors
  • Hyaluronic Acid