4.6 Article

MyD88-Dependent TLR1/2 Signals Educate Dendritic Cells with Gut-Specific Imprinting Properties

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JOURNAL OF IMMUNOLOGY
卷 187, 期 1, 页码 141-150

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1003740

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  1. Crohn's and Colitis Foundation of America
  2. National Institutes of Health [1DP2OD006512-01]
  3. Cancer Research Institute
  4. Massachusetts General Hospital
  5. Massachusetts Life Science Center

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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. The Journal of Immunology, 2011, 187: 141-150.

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