Proteomic analysis of apoptotic and oncotic pancreatic acinar AR42J cells treated with caerulein

被引:17
|
作者
Chu, Jiangtao [1 ]
Ji, Hongliang [1 ]
Lu, Ming [2 ]
Li, Zhituo [1 ]
Qiao, Xin [2 ]
Sun, Bei [1 ]
Zhang, Weihui [1 ]
Xue, Dongbo [1 ]
机构
[1] Harbin Med Univ, Dept Gen Surg, Affiliated Hosp 1, Harbin 150001, Peoples R China
[2] Univ Calif Los Angeles, Dept Surg, David Geffen Sch Med, Los Angeles, CA 90024 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Proteomics; Acute pancreatitis; Apoptosis; Oncosis; UBIQUITIN-PROTEASOME PATHWAY; ENDOPLASMIC-RETICULUM; SIGNALING PATHWAY; ARSENIC TRIOXIDE; DEATH; PROTEIN; RAT; ACTIVATION; STRESS; HMGB1;
D O I
10.1007/s11010-013-1603-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study aims to determine the differentially expressed proteins in the pancreatic acinar cells undergoing apoptosis and oncosis stimulated with caerulein to explore different cell death process of the acinar cell. AR42J cells were treated with caerulein to induce cell model of acute pancreatitis. Cells that were undergoing apoptosis and oncosis were separated by flow cytometry. Then differentially expressed proteins in the two groups of separated cells were detected by shotgun liquid chromatography-tandem mass spectrometry. The results showed that 11 proteins were detected in both apoptosis group and oncosis group, 17 proteins were detected only in apoptosis group and 29 proteins were detected only in oncosis group. KEGG analysis showed that proteins detected only in apoptosis group were significantly enriched in 10 pathways, including ECM-receptor interaction, cell adhesion molecules, and proteins detected only in oncosis group were significantly enriched in three pathways, including endocytosis, base excision repair, and RNA degradation. These proteins we detected are helpful for us to understand the process of cell death in acute pancreatitis and may be useful for changing the death mode of pancreatic acinar cells, thus attenuating the severity of pancreatitis.
引用
收藏
页码:1 / 17
页数:17
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