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Identification of dendritic cell precursor from the CD11c+ cells expressing high levels of MHC class II molecules in the culture of bone marrow with FLT3 ligand

DC Field Value Language
dc.contributor.author김태균-
dc.contributor.author나혜영-
dc.contributor.author박채규-
dc.contributor.author주민경-
dc.contributor.author박제연-
dc.date.accessioned2024-01-16T01:56:38Z-
dc.date.available2024-01-16T01:56:38Z-
dc.date.issued2023-11-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/197793-
dc.description.abstractDendritic cells (DCs) are readily generated from the culture of mouse bone marrow (BM) treated with either granulocyte macrophage-colony stimulating factor (GM-CSF) or FMS-like tyrosine kinase 3 ligand (FLT3L). CD11c+MHCII+ or CD11c+MHCIIhi cells are routinely isolated from those BM cultures and generally used as in vitro-generated DCs for a variety of experiments and therapies. Here, we examined CD11c+ cells in the BM culture with GM-CSF or FLT3L by staining with a monoclonal antibody 2A1 that is known to recognize mature or activated DCs. Most of the cells within the CD11c+MHCIIhi DC gate were 2A1+ in the BM culture with GM-CSF (GM-BM culture). In the BM culture with FLT3L (FL-BM culture), almost of all the CD11c+MHCIIhi cells were within the classical DC2 (cDC2) gate. The analysis of FL-BM culture revealed that a majority of cDC2-gated CD11c+MHCIIhi cells exhibited a 2A1-CD83-CD115+CX3CR1+ phenotype, and the others consisted of 2A1+CD83+CD115-CX3CR1- and 2A1-CD83-CD115-CX3CR1- cells. According to the antigen uptake and presentation, morphologies, and gene expression profiles, 2A1-CD83-CD115-CX3CR1- cells were immature cDC2s and 2A1+CD83+CD115-CX3CR1- cells were mature cDC2s. Unexpectedly, however, 2A1-CD83-CD115+CX3CR1+ cells, the most abundant cDC2-gated MHCIIhi cell subset in FL-BM culture, were non-DCs. Adoptive cell transfer experiments in the FL-BM culture confirmed that the cDC2-gated MHCIIhi non-DCs were precursors to cDC2s, i.e., MHCIIhi pre-cDC2s. MHCIIhi pre-cDC2s also expressed the higher level of DC-specific transcription factor Zbtb46 as similarly as immature cDC2s. Besides, MHCIIhi pre-cDC2s were generated only from pre-cDCs and common DC progenitor (CDP) cells but not from monocytes and common monocyte progenitor (cMoP) cells, verifying that MHCIIhi pre-cDC2s are close lineage to cDCs. All in all, our study identified and characterized a new cDC precursor, exhibiting a CD11c+MHCIIhiCD115+CX3CR1+ phenotype, in FL-BM culture. Copyright © 2023 In, Park, Shin, Ryu, Sohn, Choi, Park, Hwang, Park, Che, Kim, Chu, Na and Park.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherFrontiers Research Foundation-
dc.relation.isPartOfFRONTIERS IN IMMUNOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAnimals-
dc.subject.MESHBone Marrow Cells-
dc.subject.MESHBone Marrow*-
dc.subject.MESHCX3C Chemokine Receptor 1 / metabolism-
dc.subject.MESHCell Differentiation-
dc.subject.MESHDendritic Cells-
dc.subject.MESHGranulocyte-Macrophage Colony-Stimulating Factor / metabolism-
dc.subject.MESHGranulocyte-Macrophage Colony-Stimulating Factor / pharmacology-
dc.subject.MESHHistocompatibility Antigens Class II*-
dc.subject.MESHMice-
dc.subject.MESHReceptor Protein-Tyrosine Kinases / metabolism-
dc.titleIdentification of dendritic cell precursor from the CD11c+ cells expressing high levels of MHC class II molecules in the culture of bone marrow with FLT3 ligand-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Dermatology (피부과학교실)-
dc.contributor.googleauthorHyunju In-
dc.contributor.googleauthorJi Soo Park-
dc.contributor.googleauthorHyun Soo Shin-
dc.contributor.googleauthorSeul Hye Ryu-
dc.contributor.googleauthorMoah Sohn-
dc.contributor.googleauthorWanho Choi-
dc.contributor.googleauthorSejung Park-
dc.contributor.googleauthorSoomin Hwang-
dc.contributor.googleauthorJeyun Park-
dc.contributor.googleauthorLihua Che-
dc.contributor.googleauthorTae-Gyun Kim-
dc.contributor.googleauthorMin Kyung Chu-
dc.contributor.googleauthorHye Young Na-
dc.contributor.googleauthorChae Gyu Park-
dc.identifier.doi10.3389/fimmu.2023.1179981-
dc.contributor.localIdA05324-
dc.contributor.localIdA04556-
dc.contributor.localIdA01718-
dc.contributor.localIdA03950-
dc.relation.journalcodeJ03075-
dc.identifier.eissn1664-3224-
dc.identifier.pmid38094300-
dc.subject.keywordFLT3 ligand-
dc.subject.keywordGM-CSF-
dc.subject.keywordantigen presentation-
dc.subject.keywordbone marrow cells-
dc.subject.keywordcell differentiation-
dc.subject.keywordcultured cells-
dc.subject.keyworddendritic cells-
dc.subject.keywordprecursor cells-
dc.contributor.alternativeNameKim, Tae-Gyun-
dc.contributor.affiliatedAuthor김태균-
dc.contributor.affiliatedAuthor나혜영-
dc.contributor.affiliatedAuthor박채규-
dc.contributor.affiliatedAuthor주민경-
dc.citation.volume14-
dc.identifier.bibliographicCitationFRONTIERS IN IMMUNOLOGY, Vol.14, 2023-11-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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