Stabilin-1 plays a protective role against Listeria monocytogenes infection through the regulation of cytokine and chemokine production and immune cell recruitment

Virulence. 2021 Dec;12(1):2088-2103. doi: 10.1080/21505594.2021.1958606.

Abstract

Scavenger receptors are part of a complex surveillance system expressed by host cells to efficiently orchestrate innate immune response against bacterial infections. Stabilin-1 (STAB-1) is a scavenger receptor involved in cell trafficking, inflammation, and cancer; however, its role in infection remains to be elucidated. Listeria monocytogenes (Lm) is a major intracellular human food-borne pathogen causing severe infections in susceptible hosts. Using a mouse model of infection, we demonstrate here that STAB-1 controls Lm-induced cytokine and chemokine production and immune cell accumulation in Lm-infected organs. We show that STAB-1 also regulates the recruitment of myeloid cells in response to Lm infection and contributes to clear circulating bacteria. In addition, whereas STAB-1 appears to promote bacterial uptake by macrophages, infection by pathogenic Listeria induces the down regulation of STAB-1 expression and its delocalization from the host cell membrane.We propose STAB-1 as a new SR involved in the control of Lm infection through the regulation of host defense mechanisms, a process that would be targeted by bacterial virulence factors to promote infection.

Keywords: Listeria; STAB-1; infection; innate immunity; scavenger receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / immunology*
  • Cell Line
  • Chemokines / immunology*
  • Cytokines / immunology*
  • Humans
  • Listeria monocytogenes
  • Listeriosis* / immunology
  • Mice
  • Mice, Inbred C57BL
  • Receptors, Lymphocyte Homing

Substances

  • Cell Adhesion Molecules, Neuronal
  • Chemokines
  • Cytokines
  • Receptors, Lymphocyte Homing
  • STAB1 protein, human
  • Stab1 protein, mouse

Grants and funding

This work was funded by National Funds through FCT—Fundação para a Ciência e a Tecnologia, I.P., under the project UIDB/04293/2020. R.P. and J.P. were supported by doctoral fellowships from FCT (SFRH/BD/89542/2012 and SFRH/BD/86871/2012). S.S. was supported by the FCT in the framework of the CEEC-Institutional 2017 program. The authors acknowledge the support of i3S Scientific Platforms: Advanced Light Microscopy, member of the national infrastructure PPBI-Portuguese Platform of BioImaging (supported by POCI-01-0145-FEDER-022122), and Translational Cytometry Unit (Tracy);Fundação para a Ciência e a Tecnologia [UIDB/04293/2020].