Dietary glutamine supplementation improves both Th1 and Th17 responses via CARD11-mTORC1 pathway in murine model of atopic dermatitis

Int Immunopharmacol. 2024 Dec 25;143(Pt 1):113316. doi: 10.1016/j.intimp.2024.113316. Epub 2024 Oct 4.

Abstract

Glutamine (GLN) is considered an immunomodulatory nutrient, while caspase recruitment domain 11 (CARD11) is a susceptibility locus for atopic dermatitis (AD). T-cell antigen receptor (TCR)-stimulated GLN uptake requires CARD11. However, the specific pathogenesis of AD via GLN uptake remains unclear. This study aimed to elucidate the association between dietary GLN supplementation and the CARD11 pathway in the pathogenesis of AD, focusing on T helper type 1 (Th1) and Th17 cell expression in AD. Herein, wild-type (WT) mice with house dust mite epidermal-sensitized skin exhibited increased expression of interferon-gamma (IFN-gamma) and interleukin (IL)-17, whereas CARD11 deficiency impaired Th1 and Th17 responses at the same site. CARD11 is a key mediator of Th1 and Th17 expression in AD. Additionally, we suppressed mammalian target of rapamycin complex 1 (mTORC1) signaling, downstream of CARD11, to underscore the critical role of CARD11 in mediating Th1 and Th17 expression in AD. Further, dietary supplementation of GLN to CARD11-/- mice restored Th1 and Th17 responses, whereas inflammatory expression was reduced in WT mice, and p-CARD11 expression and mTORC1 signaling activity were increased in JPM50.6 cells and CARD11-/- mice. Upon inhibiting the GLN transporter, alanine-serine-cysteine transporter carrier 2 (ASCT2), we observed that the Th1 and Th17 response in AD was reduced. Conclusively, ASCT2-mediated GLN uptake improves the expression of Th1 and Th17 cells via CARD11-mTORC1 signaling pathway in AD, suggesting the potential of glutamine supplementation for AD treatment.

Keywords: ASCT2; Atopic dermatitis; CARD11; Glutamine; Th1; Th17; mTORC1.

MeSH terms

  • Amino Acid Transport System ASC / genetics
  • Amino Acid Transport System ASC / metabolism
  • Animals
  • CARD Signaling Adaptor Proteins* / genetics
  • CARD Signaling Adaptor Proteins* / metabolism
  • Dermatitis, Atopic* / drug therapy
  • Dermatitis, Atopic* / immunology
  • Dietary Supplements*
  • Disease Models, Animal*
  • Glutamine* / metabolism
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-17 / metabolism
  • Mechanistic Target of Rapamycin Complex 1* / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Minor Histocompatibility Antigens / genetics
  • Minor Histocompatibility Antigens / metabolism
  • Pyroglyphidae / immunology
  • Signal Transduction
  • Skin / drug effects
  • Skin / immunology
  • Skin / metabolism
  • Skin / pathology
  • Th1 Cells* / immunology
  • Th17 Cells* / immunology

Substances

  • Amino Acid Transport System ASC
  • CARD Signaling Adaptor Proteins
  • Card11 protein, mouse
  • Glutamine
  • Interferon-gamma
  • Interleukin-17
  • Mechanistic Target of Rapamycin Complex 1
  • Minor Histocompatibility Antigens