1. Academic Validation
  2. Interleukin-10-induced MARCH1 mediates intracellular sequestration of MHC class II in monocytes

Interleukin-10-induced MARCH1 mediates intracellular sequestration of MHC class II in monocytes

  • Eur J Immunol. 2008 May;38(5):1225-30. doi: 10.1002/eji.200737902.
Jacques Thibodeau 1 Marie-Claude Bourgeois-Daigneault Gabrielle Huppé Jessy Tremblay Angélique Aumont Mathieu Houde Eric Bartee Alexandre Brunet Marie-Elaine Gauvreau Aude de Gassart Evelina Gatti Martin Baril Maryse Cloutier Séverine Bontron Klaus Früh Daniel Lamarre Viktor Steimle
Affiliations

Affiliation

  • 1 Département de Microbiologie et Immunologie, Université de Montréal, Montréal, QC, Canada. [email protected]
Abstract

IL-10 is a potent anti-inflammatory cytokine interfering with antigen presentation by inducing the intracellular sequestration of MHC class II (MHC-II) molecules. Here we studied the contribution of membrane-associated RING-CH (MARCH) ubiquitin ligase family members to the IL-10-induced down-regulation of MHC-II molecules. We found that MARCH1 and MARCH8 proteins are the most potent family members for the down-regulation of MHC-II surface expression in transfected cells, but only MARCH1 mRNA expression is strongly induced by IL-10 in human primary monocytes. We detected mono- and poly-ubiquitinated forms of MHC-II molecules both in IL-10-treated monocytes and in cells transfected with MARCH1. We also show direct interaction between MHC-II and MARCH1 molecules in co-immunoprecipitation assays. Finally, we found that siRNA-mediated knockdown of MARCH1 reverses IL-10-induced MHC-II down-regulation in primary monocytes. Thus, the immunosuppressive effect of IL-10 on antigen presentation is mediated through induced expression of MARCH1.

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