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The UPR sensor IRE1α promotes dendritic cell responses to control Toxoplasma gondii infection
Author(s) -
Poncet Anaïs F,
Bosteels Victor,
Hoffmann Eik,
Chehade Sylia,
Rennen Sofie,
Huot Ludovic,
Peucelle Véronique,
Maréchal Sandra,
Khalife Jamal,
Blanchard Nicolas,
Janssens Sophie,
Marion Sabrina
Publication year - 2021
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.15252/embr.201949617
Subject(s) - toxoplasma gondii , xbp1 , unfolded protein response , biology , immune system , intracellular parasite , immunology , secretion , antigen , dendritic cell , immunity , regulator , virology , microbiology and biotechnology , antibody , endoplasmic reticulum , gene , rna , biochemistry , rna splicing
The unfolded protein response (UPR) has emerged as a central regulator of immune cell responses in several pathologic contexts including infections. However, how intracellular residing pathogens modulate the UPR in dendritic cells (DCs) and thereby affect T cell‐mediated immunity remains uncharacterized. Here, we demonstrate that infection of DCs with Toxoplasma gondii ( T. gondii ) triggers a unique UPR signature hallmarked by the MyD88‐dependent activation of the IRE1α pathway and the inhibition of the ATF6 pathway. Induction of XBP1s controls pro‐inflammatory cytokine secretion in infected DCs, while IRE1α promotes MHCI antigen presentation of secreted parasite antigens. In mice, infection leads to a specific activation of the IRE1α pathway, which is restricted to the cDC1 subset. Mice deficient for IRE1α and XBP1 in DCs display a severe susceptibility to T. gondii and succumb during the acute phase of the infection. This early mortality is correlated with increased parasite burden and a defect in splenic T‐cell responses. Thus, we identify the IRE1α/XBP1s branch of the UPR as a key regulator of host defense upon T. gondii infection.