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Serum amyloid A delivers retinol to intestinal myeloid cells to promote adaptive immunity

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dc.contributor.authorBang, Ye-Ji-
dc.contributor.authorHu, Zehan-
dc.contributor.authorLi, Yun-
dc.contributor.authorGattu, Sureka-
dc.contributor.authorRuhn, Kelly A.-
dc.contributor.authorRaj, Prithvi-
dc.contributor.authorHerz, Joachim-
dc.contributor.authorHooper, Lora, V-
dc.date.accessioned2023-05-03T05:44:35Z-
dc.date.available2023-05-03T05:44:35Z-
dc.date.created2022-09-13-
dc.date.created2022-09-13-
dc.date.created2022-09-13-
dc.date.issued2021-09-
dc.identifier.citationSCIENCE, Vol.373 No.6561, pp.abf9232-+-
dc.identifier.issn0036-8075-
dc.identifier.urihttps://hdl.handle.net/10371/191769-
dc.description.abstractVitamin A and its derivative retinol are essential for the development of intestinal adaptive immunity. Retinoic acid (RA)-producing myeloid cells are central to this process, but how myeloid cells acquire retinol for conversion to RA is unknown. Here, we show that serum amyloid A (SAA) proteins-retinol-binding proteins induced in intestinal epithelial cells by the microbiota-deliver retinol to myeloid cells. We identify low-density lipoprotein (LDL) receptor-related protein 1 (LRP1) as an SAA receptor that endocytoses SAA-retinol complexes and promotes retinol acquisition by RA-producing intestinal myeloid cells. Consequently, SAA and LRP1 are essential for vitamin A-dependent immunity, including B and T cell homing to the intestine and immunoglobulin A production. Our findings identify a key mechanism by which vitamin A promotes intestinal immunity.-
dc.language영어-
dc.publisherAMER ASSOC ADVANCEMENT SCIENCE-
dc.titleSerum amyloid A delivers retinol to intestinal myeloid cells to promote adaptive immunity-
dc.typeArticle-
dc.identifier.doi10.1126/science.abf9232-
dc.citation.journaltitleSCIENCE-
dc.identifier.wosid000697488600056-
dc.identifier.scopusid2-s2.0-85115177902-
dc.citation.endpage+-
dc.citation.number6561-
dc.citation.startpageabf9232-
dc.citation.volume373-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorBang, Ye-Ji-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusMEDIATES CELLULAR UPTAKE-
dc.subject.keywordPlusBINDING-PROTEIN-
dc.subject.keywordPlusMICROSCALE THERMOPHORESIS-
dc.subject.keywordPlusDENDRITIC CELL-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusTH17-
dc.subject.keywordPlusMACROPHAGES-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusRESPONSES-
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  • College of Medicine
  • Department of Medicine
Research Area Bacterial pathogenesis, Host-microbe interaction, Nutritional immunology

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