Bcat2-Mediated Branched-Chain Amino Acid Catabolism Is Linked to the Aggravated Inflammation in Obese with Psoriasis Mice

Mol Nutr Food Res. 2024 Apr;68(8):e2300720. doi: 10.1002/mnfr.202300720. Epub 2024 Apr 6.

Abstract

Scope: The global prevalence of obesity has significantly increased, presenting a major health challenge. High-fat diet (HFD)-induced obesity is closely related to the disease severity of psoriasis, but the mechanism is not fully understood.

Methods and results: The study utilizes the HFD-induced obesity model along with an imiquimod (IMQ)-induced psoriasis-like mouse model (HFD-IMQ) to conduct transcriptomics and metabolomic analyses. HFD-induced obese mice exhibits more severe psoriasis-like lesions compared to normal diet (ND)-IMQ mice. The expression of genes of the IL-17 signaling pathway (IL-17A, IL-17F, S100A9, CCL20, CXCL1) is significantly upregulated, leading to an accumulation of T cells and neutrophils in the skin. Moreover, the study finds that there is an inhibition of the branched-chain amino acids (BCAAs) catabolism pathway, and the key gene branched-chain amino transferase 2 (Bcat2) is significantly downregulated, and the levels of leucine, isoleucine, and valine are elevated in the HFD-IMQ mice. Furthermore, the study finds that the peroxisome proliferator-activated receptor gamma (PPAR γ) is inhibited, while STAT3 activity is promoted in HFD-IMQ mice.

Conclusion: HFD-induced obesity significantly amplifies IL-17 signaling and exacerbates psoriasis, with a potential role played by Bcat2-mediated BCAAs metabolism. The study suggests that BCAA catabolism and PPAR γ-STAT3 exacerbate inflammation in psoriasis with obesity.

Keywords: Bcat2, branched‐chain amino acid, healthy, obesity; psoriasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids, Branched-Chain* / metabolism
  • Animals
  • Diet, High-Fat* / adverse effects
  • Disease Models, Animal
  • Imiquimod
  • Inflammation / metabolism
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Obese
  • Obesity* / complications
  • Obesity* / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Psoriasis* / metabolism
  • Psoriasis* / pathology
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Skin / metabolism
  • Transaminases* / metabolism

Substances

  • Amino Acids, Branched-Chain
  • Imiquimod
  • Interleukin-17
  • PPAR gamma
  • Stat3 protein, mouse
  • STAT3 Transcription Factor
  • Transaminases