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Shisheng Sun

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Professor  
Supervisor of Doctorate Candidates  

Paper Publications

47. Ting Zhao, Li Jia, Jun Li, Chen Ma, Jingyu Wu, Jiechen Shen, Liuyi Dang, Bojing Zhu, Pengfei Li, Yuan Zhi, Rongxia Lan, Yintai Xu, Zhifang Hao, Yichao Chai, Qingshan Li, Liangshuo Hu, Shisheng Sun*. Heterogeneities of site-specific N-glycosylation in HCC tumors with low and high AFP concentrations. Frontiers in Oncology. 2020, 10: 496.

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Impact Factor7.561

DOI number:10.3389/fimmu.2021.700009

Key Words:cell model; macrophage; mass spectrometry; polarization; proteomics.

Abstract: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.

Indexed by:Journal paper

Discipline:Natural Science

First-Level Discipline:Biology

Translation or Not:no

Included Journals:SCI

Pre One:48. Jun Li, Li Jia, Zhifang Hao, Yintai Xu, Jiechen Shen, Chen Ma, Jingyu Wu, Ting Zhao, Yuan Zhi, Pengfei Li, Jing Li, Bojing Zhu, Shisheng Sun*. Site-specific N-glycoproteme Analysis Reveals Up-regulated Sialylation and Core Fucosylation during Transient Regeneration Loss in Neonatal Mouse Hearts. Journal of Proteome Research. 2020. 19 (8): 3191–3200.

Next One:46. Rongxia Lan#, Miaomiao Xin#, Zhifang Hao, Shanshan You, Yintai Xu, Jingyu Wu, Liuyi Dang, Xinwen Zhang, Shisheng Sun*. Biological Functions and Large-Scale Profiling of Protein Glycosylation in Human Semen. Journal of proteome research. 2020, 19 (10): 3877-3889.