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MyD88-Dependent TLR1/2 Signals Educate Dendritic Cells with Gut-Specific Imprinting Properties
Author(s) -
Sen Wang,
Eduardo J. Villablanca,
Jaime De Calisto,
Daniel Cláudio Oliveira Gomes,
Deanna D. Nguyen,
Emiko Mizoguchi,
Jonathan C. Kagan,
Hans-Christian Reinecker,
Nir Hacohen,
Cathryn R. Nagler,
Ramnik J. Xavier,
Bartira RossiBergmann,
YiBin Chen,
Rune Blomhoff,
Scott B. Snapper,
J. Rodrigo Mora
Publication year - 2011
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1003740
Subject(s) - tlr2 , gut flora , dendritic cell , homing (biology) , microbiology and biotechnology , retinoic acid , imprinting (psychology) , biology , agonist , chemistry , receptor , immunology , immune system , signal transduction , biochemistry , gene , ecology , tlr4
Gut-associated dendritic cells (DC) synthesize all-trans retinoic acid, which is required for inducing gut-tropic lymphocytes. Gut-associated DC from MyD88(-/-) mice, which lack most TLR signals, expressed low levels of retinal dehydrogenases (critical enzymes for all-trans retinoic acid biosynthesis) and were significantly impaired in their ability to induce gut-homing T cells. Pretreatment of extraintestinal DC with a TLR1/2 agonist was sufficient to induce retinal dehydrogenases and to confer these DC with the capacity to induce gut-homing lymphocytes via a mechanism dependent on MyD88 and JNK/MAPK. Moreover, gut-associated DC from TLR2(-/-) mice, or from mice in which JNK was pharmacologically blocked, were impaired in their education to imprint gut-homing T cells, which correlated with a decreased induction of gut-tropic T cells in TLR2(-/-) mice upon immunization. Thus, MyD88-dependent TLR2 signals are necessary and sufficient to educate DC with gut-specific imprinting properties and contribute in vivo to the generation of gut-tropic T cells.

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