树突状细胞
浆细胞样树突状细胞
生物
造血
细胞生物学
脐带血
免疫系统
祖细胞
免疫学
滤泡树突状细胞
间质细胞
获得性免疫系统
体外
干细胞
抗原提呈细胞
T细胞
癌症研究
生物化学
作者
Xinlong Luo,Sreekumar Balan,Catharina Arnold‐Schrauf,Marc Dalod
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 133-145
被引量:2
标识
DOI:10.1007/978-1-0716-2938-3_10
摘要
Dendritic cells (DCs) represent one of the most important immune cell subsets in preventing the host from pathogen invasion by promoting both innate and adaptive immunity. Most research on human dendritic cells has focused on the easy-to-obtain dendritic cells derived in vitro from monocytes (MoDCs). However, many questions remain unanswered regarding the role of different dendritic cell types. The investigation of their roles in human immunity is hampered by their rarity and fragility, which especially holds true for type 1 conventional dendritic cells (cDC1s) and for plasmacytoid dendritic cells (pDCs). In vitro differentiation from hematopoietic progenitors emerged as a common way to produce different DC types, but the efficiency and reproducibility of these protocols needed to be improved and the extent to which the DCs generated in vitro resembled their in vivo counterparts required a more rigorous and global assessment. Here, we describe a cost-effective and robust in vitro differentiation system for the production of cDC1s and pDCs equivalent to their blood counterparts, from cord blood CD34+ hematopoietic stem cells (HSCs) cultured on a stromal feeder layer with a combination of cytokines and growth factors.
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