Affiliation:
1. Department of Gastroenterology, Chengdu First People’s Hospital, Chengdu, Sichuan, 610016, China
2. Department of Western Pharmacy, Chengdu First People’s Hospital, Chengdu, Sichuan, 610016, China
Abstract
Bone marrow mesenchymal stem cells (BMSCs) are capable of multipolar differentiation and repairing injured tissues. Herein, we aimed to investigate the mechanism by how BMSCs modulate the apoptotic pathway in the acute pancreatitis (AP). In this study, primary BMSCs were cultured and administrated into 10 AP mice while 10 healthy mice were taken as a blank group and 10 AP mice as a control group. The mouse pancreatic tissues were assessed by HE staining and evaluated by pancreatitis score and serum amylase detection. Level of inflammatory factors CRP and TNF-αwas measured by ELISA and PIPK1, PIPK3, MLKL and Caspase-8 expression was detected by RT-qPCR and Western blot. The pancreatitis score (7.29±1.36) and the serum amylase score of (453.66±103.67) mu/ml of BMSCs group was significantly higher than that of control group, indicating increased tissue repair after BMSCs treatment. BMSCs group exhibited a higher level of CRP (711.01±115.31) and TNF-α(132.81±22.13) in serum compared to control group (p< 0.05). PIPK1, PIPK3, and MLKL expression in BMSCs group decreased (p< 0.05) whereas Caspase-8 was increased (p< 0.05). On the other hand, BMSCs group presented upregulated PIPK1, PIPK3, and MLKL (p< 0.05) and downregulated Caspase-8 (p< 0.05). In conclusion, BMSCs regulate cell apoptosis by upregulating Caspase-8 expression, and downregulating PIPK1, PIPK3 and MLKL level, thereby alleviating the inflammation in AP.
Publisher
American Scientific Publishers
Subject
Biomedical Engineering,Medicine (miscellaneous),Bioengineering,Biotechnology