HEK 293细胞
细胞培养
先天免疫系统
细胞生物学
树突状细胞
生物
粒细胞巨噬细胞集落刺激因子
重组DNA
分子生物学
免疫系统
免疫学
细胞因子
生物化学
基因
遗传学
作者
Elektra K. Robinson,Sergio Covarrubias,Simon K. Zhou,Susan Carpenter
出处
期刊:PLOS ONE
[Public Library of Science]
日期:2021-04-09
卷期号:16 (4): e0249117-e0249117
被引量:4
标识
DOI:10.1371/journal.pone.0249117
摘要
Macrophages and dendritic cells (DCs) are innate immune cells that play a key role in defense against pathogens. In vitro cultures of bone marrow-derived macrophages (BMDMs) and dendritic cells (BMDCs) are well-established and valuable methods for immunological studies. Typically, commercially available recombinant GM-CSF is utilized to generate BMDCs and is also used to culture alveolar macrophages. We have generated a new HEK-293T cell line expressing murine GM-CSF that secretes high levels of GM-CSF (~180 ng/ml) into complete media as an alternative to commercial GM-CSF. Differentiation of dendritic cells and expression of various markers were kinetically assessed using the GM-CSF HEK293T cell line, termed supGM-CSF and compared directly to purified commercial GMCSF. After 7–9 days of cell culture the supGM-CSF yielded twice as many viable cells compared to the commercial purified GM-CSF. In addition to differentiating BMDCs, the supGM-CSF can be utilized to culture functionally active alveolar macrophages. Collectively, our results show that supernatant from our GM-CSF HEK293T cell line supports the differentiation of mouse BMDCs or alveolar macrophage culturing, providing an economical alternative to purified GM-CSF.
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