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
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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