Original Article
Copyright ©2013 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Apr 14, 2013; 19(14): 2179-2186
Published online Apr 14, 2013. doi: 10.3748/wjg.v19.i14.2179
Involvement of interstitial cells of Cajal in experimental severe acute pancreatitis in rats
Liang-Liang Shi, Ming-Dong Liu, Min Chen, Xiao-Ping Zou
Liang-Liang Shi, Ming-Dong Liu, Min Chen, Xiao-Ping Zou, Department of Gastroenterology, Medical School, the Affiliated Drum Tower Hospital of Nanjing University, Nanjing 210008, Jiangsu Province, China
Author contributions: Liu MD and Zou XP contributed equally to this work; Shi LL, Liu MD and Chen M designed and performed the research; Chen M provided analytical tools and was also involved in editing the manuscript; Shi LL analyzed the data, as well as writing the paper.
Correspondence to: Xiao-Ping Zou, MD, Professor, Department of Gastroenterology, Medical School, the Affiliated Drum Tower Hospital of Nanjing University, Nanjing 210008, Jiangsu Province, China. 13770771661@163.com
Telephone: +86-25-83105206 Fax: +86-25-83105206
Received: November 21, 2012
Revised: December 11, 2012
Accepted: February 5, 2013
Published online: April 14, 2013
Processing time: 143 Days and 19.8 Hours
Abstract

AIM: To observe the changes in interstitial cells of Cajal (ICC) in rats with experimental severe acute pancreatitis (SAP).

METHODS: A total of twenty-four SD rats were randomly divided into two groups (n = 12), namely the sham (S) group and the SAP group; the SAP rat model was established by retrograde injection of 5% sodium taurocholate (1.0 mL/kg) into the pancreatic duct. Twenty-four hours later intestinal motility was assessed by testing small intestinal propulsion rate, and then the rats were sacrificed. The pancreas and jejunum were resected and underwent routine pathologic examination. Immunohistochemical staining was used to detect c-kit-positive cells in the jejunum. Expression of c-kit mRNA was detected by real-time polymerase chain reaction, and the expression of c-kit protein was evaluated by Western blotting. Ultrastructure of ICC was evaluated by transmission electron microscopy.

RESULTS: There was bleeding, necrosis and a large amount of inflammatory cell infiltration in pancreatic tissue in the SAP group, while in jejunal tissue we observed a markedly denuded mucosal layer, loss of villous tissue and a slightly dilated muscular layer. The small intestinal propulsion rate was 68.66% ± 2.66% in the S group and 41.55% ± 3.85% in the SAP group. Compared with the S group, the rate of the SAP group decreased sharply. The density of c-kit-positive cells in the SAP group was significantly lower than in the S group; the respective mean densities were 88.47 ± 10.49 in the S group and 56.11 ± 7.09 in the SAP group. The levels of c-kit protein and mRNA were 0.36 ± 0.04 and 1.29 ± 0.91 in the SAP group, respectively, which were significantly lower than those in the S group (0.53 ± 0.06, 0.64 ± 0.33, respectively). In the SAP group, ICC profiles showed the same change tendency, such as vacuolation of mitochondria, irregular vacuoles and loosened desmosome-like junctions.

CONCLUSION: Decreased c-kit-positive cells and ultrastructural changes in ICC resulting from blockade of the c-kit signaling pathway are involved in the intestinal dysmotility associated with SAP.

Keywords: Severe acute pancreatitis; c-kit; Interstitial cells of Cajal; Real-time polymerase chain reaction; Ultrastructure