Ruminococcus gnavus and Limosilactobacillus reuteri Regulate Reg3γ Expression through Multiple Pathways.

Autor: Ramirez ZE; Division of Infectious Diseases, Department of Pediatrics, Duke University School of Medicine, Durham, NC.; Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC., Surana NK; Division of Infectious Diseases, Department of Pediatrics, Duke University School of Medicine, Durham, NC.; Department of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC.; Department of Immunology, Duke University School of Medicine, Durham, NC.
Jazyk: angličtina
Zdroj: ImmunoHorizons [Immunohorizons] 2023 Mar 01; Vol. 7 (3), pp. 228-234.
DOI: 10.4049/immunohorizons.2200096
Abstrakt: Epithelium-derived antimicrobial peptides represent an evolutionarily ancient defense mechanism against pathogens. Regenerating islet-derived protein 3 γ (Reg3γ), the archetypal intestinal antimicrobial peptide, is critical for maintaining host-microbe interactions. Expression of Reg3γ is known to be regulated by the microbiota through two different pathways, although it remains unknown whether specific Reg3γ-inducing bacteria act via one or both of these pathways. In recent work, we identified Ruminococcus gnavus and Limosilactobacillus reuteri as commensal bacteria able to induce Reg3g expression. In this study, we show these bacteria require myeloid differentiation primary response protein 88 and group 3 innate lymphoid cells for induction of Reg3γ in mice. Interestingly, we find that R. gnavus and L. reuteri suppress Reg3γ in the absence of either myeloid differentiation primary response protein 88 or group 3 innate lymphoid cells. In addition, we demonstrate that colonization by these bacteria is not required for induction of Reg3γ, which occurs several days after transient exposure to the organisms. Taken together, our findings highlight the complex mechanisms underlying microbial regulation of Reg3γ.
(Copyright © 2023 The Authors.)
Databáze: MEDLINE