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

CD11c公司 树突状细胞 CD40 滤泡树突状细胞 骨髓 化学 抗原提呈细胞 白细胞介素12 MHC II级 细胞生物学 分子生物学 生物 主要组织相容性复合体 T细胞 抗原 细胞毒性T细胞 免疫学 免疫系统 体外 表型 生物化学 基因
作者
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
出处
期刊:Frontiers in Immunology [Frontiers Media]
卷期号:14: 1179981-1179981 被引量:4
标识
DOI:10.3389/fimmu.2023.1179981
摘要

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 + MHCII hi 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 + MHCII hi 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 + MHCII hi cells were within the classical DC2 (cDC2) gate. The analysis of FL-BM culture revealed that a majority of cDC2-gated CD11c + MHCII hi cells exhibited a 2A1 - CD83 - CD115 + CX 3 CR1 + phenotype, and the others consisted of 2A1 + CD83 + CD115 - CX 3 CR1 - and 2A1 - CD83 - CD115 - CX 3 CR1 - cells. According to the antigen uptake and presentation, morphologies, and gene expression profiles, 2A1 - CD83 - CD115 - CX 3 CR1 - cells were immature cDC2s and 2A1 + CD83 + CD115 - CX 3 CR1 - cells were mature cDC2s. Unexpectedly, however, 2A1 - CD83 - CD115 + CX 3 CR1 + cells, the most abundant cDC2-gated MHCII hi cell subset in FL-BM culture, were non-DCs. Adoptive cell transfer experiments in the FL-BM culture confirmed that the cDC2-gated MHCII hi non-DCs were precursors to cDC2s, i.e., MHCII hi pre-cDC2s. MHCII hi pre-cDC2s also expressed the higher level of DC-specific transcription factor Zbtb46 as similarly as immature cDC2s. Besides, MHCII hi 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 MHCII hi pre-cDC2s are close lineage to cDCs. All in all, our study identified and characterized a new cDC precursor, exhibiting a CD11c + MHCII hi CD115 + CX 3 CR1 + phenotype, in FL-BM culture.
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