期刊
JOURNAL OF LIPID RESEARCH
卷 54, 期 9, 页码 2525-2542出版社
ELSEVIER
DOI: 10.1194/jlr.M040212
关键词
primary macrophage; toll-like receptor 4; transcriptomics; lipidomics; inflammation; lipid and signaling networks; cell cycle; correlation analysis
资金
- National Institute of General [U54 GM-69338]
- National Science Foundation [DBI-0835541, STC-0939370]
- National Institutes of Health [R01HL-106579, R01HL-108735]
- Direct For Biological Sciences
- Div Of Biological Infrastructure [0835541] Funding Source: National Science Foundation
Studies of macrophage biology have been significantly advanced by the availability of cell lines such as RAW264.7 cells. However, it is unclear how these cell lines differ from primary macrophages such as thioglycolate-elicited peritoneal macrophages (TGEMs). We used the inflammatory stimulus Kdo(2)-lipid A (KLA) to stimulate RAW264.7 and TGEM cells. Temporal changes of lipid and gene expression levels were concomitantly measured and a systems-level analysis was performed on the fold-change data. Here we present a comprehensive comparison between the two cell types. Upon KLA treatment, both RAW264.7 and TGEM cells show a strong inflammatory response. TGEM (primary) cells show a more rapid and intense inflammatory response relative to RAW264.7 cells. DNA levels (fold-change relative to control) are reduced in RAW264.7 cells, correlating with greater downregulation of cell cycle genes. The transcriptional response suggests that the cholesterol de novo synthesis increases considerably in RAW264.7 cells, but 25-hydroxycholesterol increases considerably in TGEM cells.jlr Overall, while RAW264.7 cells behave similarly to TGEM cells in some ways and can be used as a good model for inflammation-and immune function-related kinetic studies, they behave differently than TGEM cells in other aspects of lipid metabolism and phenotypes used as models for various disorders such as atherosclerosis.
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