孙士生

个人信息:Personal Information

教授
博士生导师
硕士生导师

教师英文名称:Shisheng Sun

教师拼音名称:sunshisheng

所在单位:生命科学学院

办公地点:西北大学太白校区,新生命科学学院2层

职称:教授

学科:生物化学与分子生物学
细胞生物学
生物学其他专业

论文成果

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51. Pengfei Li#, Zhifang Hao#, Jingyu Wu, Chen Ma, Yintai Xu, Jun Li, Rongxia Lan, Bojing Zhu, Pengyu Ren, Daidi Fan, Shisheng Sun*. Comparative Proteomic Analysis of Polarized Human THP-1 and Mouse RAW264. 7 Macrophages. Frontiers in immunology. 2021, 12: 700009.

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影响因子:7.561

DOI码:10.3389/fimmu.2021.700009

关键字:cell model; macrophage; mass spectrometry; polarization; proteomics.

摘要:Macrophages can be polarized into classically activated macrophages (M1) and alternatively activated macrophages (M2) in the immune system, performing pro-inflammatory and anti-inflammatory functions, respectively. Human THP-1 and mouse RAW264.7 cell line models have been widely used in various macrophage-associated studies, while the similarities and differences in protein expression profiles between the two macrophage models are still largely unclear. In this study, the protein expression profiles of M1 and M2 phenotypes from both THP-1 and RAW264.7 macrophages were systematically investigated using mass spectrometry-based proteomics. By quantitatively analyzing more than 5,000 proteins among different types of macrophages (M0, M1 and M2) from both cell lines, we identified a list of proteins that were uniquely up-regulated in each macrophage type and further confirmed 43 proteins that were commonly up-regulated in M1 macrophages of both cell lines. These results revealed considerable divergences of each polarization type between THP-1 and RAW264.7 macrophages. Moreover, the mRNA and protein expression of CMPK2, RSAD2, DDX58, and DHX58 were strongly up-regulated in M1 macrophages for both macrophage models. These data can serve as important resources for further studies of macrophage-associated diseases in experimental pathology using human and mouse cell line models.

论文类型:期刊论文

学科门类:理学

一级学科:生物学

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收录刊物:SCI