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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

Authors
 Hyunju In  ;  Ji Soo Park  ;  Hyun Soo Shin  ;  Seul Hye Ryu  ;  Moah Sohn  ;  Wanho Choi  ;  Sejung Park  ;  Soomin Hwang  ;  Jeyun Park  ;  Lihua Che  ;  Tae-Gyun Kim  ;  Min Kyung Chu  ;  Hye Young Na  ;  Chae Gyu Park 
Citation
 FRONTIERS IN IMMUNOLOGY, Vol.14, 2023-11 
Journal Title
FRONTIERS IN IMMUNOLOGY
Issue Date
2023-11
MeSH
Animals ; Bone Marrow Cells ; Bone Marrow* ; CX3C Chemokine Receptor 1 / metabolism ; Cell Differentiation ; Dendritic Cells ; Granulocyte-Macrophage Colony-Stimulating Factor / metabolism ; Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology ; Histocompatibility Antigens Class II* ; Mice ; Receptor Protein-Tyrosine Kinases / metabolism
Keywords
FLT3 ligand ; GM-CSF ; antigen presentation ; bone marrow cells ; cell differentiation ; cultured cells ; dendritic cells ; precursor cells
Abstract
Dendritic 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.
Files in This Item:
T202307499.pdf Download
DOI
10.3389/fimmu.2023.1179981
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
Yonsei Authors
Kim, Tae-Gyun(김태균) ORCID logo https://orcid.org/0000-0002-2116-4579
Na, Hye Young(나혜영) ORCID logo https://orcid.org/0000-0002-2886-9926
Park, Jeyun(박제연)
Park, Chae Gyu(박채규) ORCID logo https://orcid.org/0000-0003-1906-1308
Chu, Min Kyung(주민경) ORCID logo https://orcid.org/0000-0001-6221-1346
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/197793
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