Toll-like Receptor 9 Pathway Mediates Schlafen+-MDSC Polarization During Helicobacter-induced Gastric Metaplasias

Gastroenterology. 2022 Aug;163(2):411-425.e4. doi: 10.1053/j.gastro.2022.04.031. Epub 2022 Apr 26.

Abstract

Background & aims: A subset of myeloid-derived suppressor cells (MDSCs) that express murine Schlafen4 (SLFN4) or its human ortholog SLFN12L polarize in the Helicobacter-inflamed stomach coincident with intestinal or spasmolytic polypeptide-expressing metaplasia. We propose that individuals with a more robust response to damage-activated molecular patterns and increased Toll-like receptor 9 (TLR9) expression are predisposed to the neoplastic complications of Helicobacter infection.

Methods: A mouse or human Transwell co-culture system composed of dendritic cells (DCs), 2-dimensional gastric epithelial monolayers, and Helicobacter were used to dissect the cellular source of interferon-α (IFNα) in the stomach by flow cytometry. Conditioned media from the co-cultures polarized primary myeloid cells. MDSC activity was determined by T-cell suppression assays. In human subjects with intestinal metaplasia or gastric cancer, the rs5743836 TLR9T>C variant was genotyped and linked to TLR9, IFNα, and SLFN12L expression by immunohistochemistry. Nuclear factor-κB binding to the TLR9 C allele was determined by electrophoretic mobility shift assays.

Results: Helicobacter infection induced gastric epithelial and plasmacytoid DC expression of TLR9 and IFNα. Co-culturing primary mouse or human cells with DCs and Helicobacter induced TLR9, IFNα secretion, and SLFN+-MDSC polarization. Neutralizing IFNα in vivo mitigated Helicobacter-induced spasmolytic polypeptide-expressing metaplasia. The TLR9 minor C allele creates a nuclear factor-κB binding site associated with higher levels of TLR9, IFNα, and SLFN12L in Helicobacter-infected stomachs that correlated with a greater incidence of metaplasias and cancer.

Conclusions: TLR9 plays an essential role in the production of IFNα and polarization of SLFN+ MDSCs on Helicobacter infection. Subjects carrying the rs5743836 TLR9 minor C allele are predisposed to neoplastic complications if chronically infected.

Keywords: 2-D Organoid-Derived Monolayer; DAMPs; IFNα; Plasmacytoid Dendritic Cells; SPEM.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Helicobacter
  • Helicobacter Infections* / genetics
  • Helicobacter Infections* / metabolism
  • Humans
  • Interferon-alpha
  • Metaplasia
  • Mice
  • Myeloid-Derived Suppressor Cells*
  • NF-kappa B / metabolism
  • Stomach Neoplasms* / genetics
  • Stomach Neoplasms* / microbiology
  • Toll-Like Receptor 4
  • Toll-Like Receptor 9* / genetics
  • Toll-Like Receptor 9* / metabolism

Substances

  • Interferon-alpha
  • NF-kappa B
  • TLR4 protein, human
  • Toll-Like Receptor 4
  • Toll-Like Receptor 9