Functional Role of MicroRNA-19b in Acinar Cell Necrosis in Acute Necrotizing Pancreatitis

被引:11
作者
Hu, Ming-xing [1 ,2 ]
Zhang, Hong-wei [2 ]
Fu, Qiang [2 ]
Qin, Tao [2 ]
Liu, Chuan-jiang [2 ]
Wang, Yu-zhu [2 ]
Tang, Qiang [2 ]
Chen, Yu-xin [1 ]
机构
[1] Shandong Univ, Shandong Qilu Hosp, Dept Hepatobiliary Pancreat Surg, Jinan 250000, Peoples R China
[2] Zhengzhou Univ, Sch Med, Peoples Hosp, Dept Hepatobiliary Pancreat Surg, Zhengzhou 450003, Peoples R China
关键词
miRNA-19b; acute pancreatitis; acinar cells; necrosis; EXPRESSION; INJURY; RATS;
D O I
10.1007/s11596-016-1570-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The expression of microRNA-19b (miR-19b) in acute necrotizing pancreatitis (ANP) and its functional role in acinar cell necrosis of SD rats were investigated. Twelve SD rats were divided into two groups randomly, including control group and ANP group. The rat ANP models were established by intraperitoneal injection of L-arginine (2400 mg/kg body weight), and equal volume of 0.9% NaCl was injected in the control group. MiRNA chip assay was performed to examine the expression of miRNAs in the pancreas in two different groups. Besides, to further explore the role of miR-19b in ANP in vitro, taurolithocholic acid 3-sulfate disodium salt (TLC-S) (200 mu mol/L) was administrated to treat the rat pancreatic acinar cell line, AR42J, for establishing the ANP cells model. The quantitative real-time PCR (qRT-PCR) was adopted to measure the miR-19b expression. Moreover, the mimic miRNA, miRNA antisense oligonucleotide (AMO) and control vector were used to transfect AR42J cells, the expression of miR-19b was confirmed by qRT-PCR and the necrotizing rate of AR42J cells was detected with AO/EB method. The expression of miR-19b was significantly higher in ANP group than in control group as displayed by the miRNA chip assay. Furthermore, after inducing necrosis of AR42J cells in vitro, the expression of miR-19b was significantly increased by 2.51 +/- 0.14 times in comparison with the control group. As revealed by qRT-PCR assay, the expression of miR-19b was 5.94 +/- 0.95 times higher in the mimic miRNA group than in the control vector group, companied with an obviously increased acinar cell necrotizing rate (50.3%+/- 1.5% vs. 39.6%+/- 2.3%, P<0.05). Moreover, the expression of miR-19b in the miRNA AMO group was 0.38 +/- 0.15 times lower than in the control vector group, and the cell necrosis rate was much lower accordingly (23.1%+/- 3.3% vs. 39.6%+/- 2.3%, P<0.05). Besides, there was no significant difference between the control vector cells and the cells without treatment (P > 0.05). The expression of miR-19b was significantly induced in ANP. In addition, up-regulation of miR-19b could promote the necrosis of pancreatic acinar cells and miR-19b deficiency could decrease the rate of pancreatic acinar cell necrosis.
引用
收藏
页码:221 / 225
页数:5
相关论文
共 16 条
[1]
Classification of acute pancreatitis-2012: revision of the Atlanta classification and definitions by international consensus [J].
Banks, Peter A. ;
Bollen, Thomas L. ;
Dervenis, Christos ;
Gooszen, Hein G. ;
Johnson, Colin D. ;
Sarr, Michael G. ;
Tsiotos, Gregory G. ;
Vege, Santhi Swaroop .
GUT, 2013, 62 (01) :102-111
[2]
MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]
Calcium and Reactive Oxygen Species in Acute Pancreatitis: Friend or Foe? [J].
Booth, David M. ;
Mukherjee, Rajarshi ;
Sutton, Robert ;
Criddle, David N. .
ANTIOXIDANTS & REDOX SIGNALING, 2011, 15 (10) :2683-2698
[4]
Gene regulation by microRNAs [J].
Carthew, RW .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2006, 16 (02) :203-208
[5]
miR-19b promotes tumor growth and metastasis via targeting TP53 [J].
Fan, Yu ;
Yin, Shenyi ;
Ha, Yang ;
Yang, Junyu ;
Zhang, Hanshuo ;
Sun, Changhong ;
Ma, Ming ;
Chang, Qing ;
Xi, Jianzhong Jeff .
RNA, 2014, 20 (06) :765-772
[6]
Evaluation of miR-216a and miR-217 as potential biomarkers of acute pancreatic injury in rats and mice [J].
Goodwin, David ;
Rosenzweig, Barry ;
Zhang, Jun ;
Xu, Lin ;
Stewart, Sharron ;
Thompson, Karol ;
Rouse, Rodney .
BIOMARKERS, 2014, 19 (06) :517-529
[7]
Reg4 protects against acinar cell necrosis in experimental pancreatitis [J].
Hu, Guoyong ;
Shen, Jiaqing ;
Cheng, Li ;
Guo, Chuanyong ;
Xu, Xuanfu ;
Wang, Feng ;
Huang, Li ;
Yang, Lijuan ;
He, Miao ;
Xiang, Di ;
Zhu, Shunying ;
Wu, Mingyuan ;
Yu, Yan ;
Han, Wei ;
Wang, Xingpeng .
GUT, 2011, 60 (06) :820-828
[8]
Duration of injury correlates with necrosis in caerulein-induced experimental acute pancreatitis: implications for pathophysiology [J].
Jacob, Tony G. ;
Raghav, Rahul ;
Kumar, Ajay ;
Garg, Pramod K. ;
Roy, Tara S. .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2014, 95 (03) :199-208
[9]
RELATIONSHIP BETWEEN SEVERITY, NECROSIS, AND APOPTOSIS IN 5 MODELS OF EXPERIMENTAL ACUTE-PANCREATITIS [J].
KAISER, AM ;
SALUJA, AK ;
SENGUPTA, A ;
SALUJA, M ;
STEER, ML .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1995, 269 (05) :C1295-C1304
[10]
Inhibitory effects of microRNA 19b in hepatic stellate cell-mediated fibrogenesis [J].
Lakner, Ashley M. ;
Steuerwald, Nury M. ;
Walling, Tracy L. ;
Ghosh, Sriparna ;
Li, Ting ;
McKillop, Iain H. ;
Russo, Mark W. ;
Bonkovsky, Herbert L. ;
Schrum, Laura W. .
HEPATOLOGY, 2012, 56 (01) :300-310