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

被引:0
|
作者
Jiangtao Chu
Hongliang Ji
Ming Lu
Zhituo Li
Xin Qiao
Bei Sun
Weihui Zhang
Dongbo Xue
机构
[1] The First Affiliated Hospital of Harbin Medical University,Department of General Surgery
[2] University of Califonia at Los Angeles,Department of Surgery, David Geffen School of Medicine
来源
关键词
Proteomics; Acute pancreatitis; Apoptosis; Oncosis;
D O I
暂无
中图分类号
学科分类号
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:16
相关论文
共 50 条
  • [1] Proteomic analysis of apoptotic and oncotic pancreatic acinar AR42J cells treated with caerulein
    Chu, Jiangtao
    Ji, Hongliang
    Lu, Ming
    Li, Zhituo
    Qiao, Xin
    Sun, Bei
    Zhang, Weihui
    Xue, Dongbo
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2013, 382 (1-2) : 1 - 17
  • [2] EFFECT OF SUBSTRATUM ON DIFFERENTIATION OF CULTURED PANCREATIC ACINAR AR42J CELLS
    HART, TK
    TOLBERT, C
    OLIVER, C
    JOURNAL OF CELL BIOLOGY, 1986, 103 (05): : A381 - A381
  • [3] Emodin attenuates cell injury and inflammation in pancreatic acinar AR42J cells
    Zhao, Jia-Yu
    Wang, Jia-Qi
    Wu, Li
    Zhang, Feng
    Chen, Zhi-Peng
    Li, Wei-Dong
    Cai, Hao
    Liu, Xiao
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2019, 21 (02) : 186 - 195
  • [4] Effects of bradykinin on the intracellular calcium concentration of pancreatic acinar AR42J cells
    Saito, Y
    Kato, M
    Kobayashi, I
    Tatemoto, K
    LIFE SCIENCES, 1996, 58 (18) : 1569 - 1574
  • [5] Early proteome analysis of rat pancreatic acinar AR42J cells treated with taurolithocholic acid 3-sulfate
    Li, Zhituo
    Lu, Ming
    Chu, Jiangtao
    Qiao, Xin
    Meng, Xianzhi
    Sun, Bei
    Zhang, Weihui
    Xue, Dongbo
    PANCREATOLOGY, 2012, 12 (03) : 248 - 256
  • [6] GLUCOCORTICOIDS REGULATE AMYLASE GENE-TRANSCRIPTION IN PANCREATIC ACINAR AR42J CELLS
    LOGSDON, CD
    PEROT, KJ
    MCDONALD, AR
    FEDERATION PROCEEDINGS, 1987, 46 (06) : 2016 - 2016
  • [7] GROWTH AND DIFFERENTIATION OF PANCREATIC ACINAR-CELLS - INDEPENDENT EFFECTS OF GLUCOCORTICOIDS ON AR42J CELLS
    GUTHRIE, J
    WILLIAMS, JA
    LOGSDON, CD
    PANCREAS, 1991, 6 (05) : 506 - 513
  • [8] GLUCOCORTICOIDS INCREASE CHOLECYSTOKININ RECEPTORS AND AMYLASE SECRETION IN PANCREATIC ACINAR AR42J CELLS
    LOGSDON, CD
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1986, 261 (05) : 2096 - 2101
  • [9] Pancreatic acinar AR42J cells express functional nerve growth factor receptors
    Miralles, F
    Czernichow, P
    Scharfmann, R
    JOURNAL OF ENDOCRINOLOGY, 1999, 160 (03) : 433 - 442
  • [10] CHARACTERIZATION OF ANGIOTENSIN-II RECEPTOR SUBTYPES IN PANCREATIC ACINAR AR42J CELLS
    CHAPPELL, MC
    JACOBSEN, DW
    TALLANT, EA
    PEPTIDES, 1995, 16 (04) : 741 - 747