Role of Microvesicles From Bone Marrow Mesenchymal Stem Cells in Acute Pancreatitis
Role of Microvesicles From Bone Marrow Mesenchymal Stem Cells in Acute Pancreatitis
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骨髓间充质干细胞微泡在急性胰腺炎中的作用
DOI:
10.1097/mpa.0000000000000694
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发表时间:
2016-10
期刊:
影响因子:
2.9
通讯作者:
Wang Xingpeng
中科院分区:
文献类型:
--
作者:
Yin Guojian;Hu Guoyong;Wan Rong;Yu Ge;Cang Xiaofeng;Xiong Jie;Ni Jianbo;Hu Yanling;Xing Miao;Fan Yuting;Xiao Wenqin;Qiu Lei;Tang Maochun;Zhao Yan;Wang Shaofeng;Wang Xingpeng
Objectives Mesenchymal stem cells (MSCs) have shown an obvious protective effect on acute pancreatitis (AP). The purpose of the present study was to analyze the effect of bone marrow MSC-derived microvesicles (bmMSC-MVs) on AP and explore the underlying mechanisms. Methods Bone marrow MSCs and bmMSC-MVs were isolated from Sprague-Dawley rats. Cerulein-induced mild AP (MAP) and sodium taurocholate-induced severe AP (SAP) were used as AP models in vivo and in vitro. Pancreatic injury was evaluated by measuring serum levels of amylase, lipase, chemokines, and interleukins, and by pancreatic histology, reverse transcription-polymerase chain reaction, Western blotting, and immunohistochemistry. The effects of bmMSC-MVs on the survival rates of pancreatic acinar cells in vitro were also assessed. Results Bone marrow MSC-MVs attenuated acute pancreatic injury in MAP and SAP by regulating IL-1&agr;, IL-6, and TNF-&agr;, and dramatically attenuated the nuclear translocation of NF-&kgr;B p65 in MAP and SAP. Bone marrow MSC-MVs improved the survival rates of pancreatic acinar cells in MAP and SAP models in vitro. Conclusions Bone marrow MSC-MVs played a protective role in AP by reducing the levels of proinflammatory cytokines and regulating the nuclear translocation of NF-&kgr;B p65. Bone marrow MSC-MVs could be developed as a strategy for the clinical treatment of SAP.
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DOI:
10.1681/asn.2011050503
发表时间:
2012-02
期刊:
Journal of the American Society of Nephrology : JASN
影响因子:
--
作者:
Sang-Won Park;Mihwa Kim;K. Brown;D. VivetteD.;Agati;H. Lee
通讯作者:
Sang-Won Park;Mihwa Kim;K. Brown;D. VivetteD.;Agati;H. Lee
影响因子:
5.2
作者:
Zhu, Ying-gang;Feng, Xiao-mei;Abbott, Jason;Fang, Xiao-hui;Hao, Qi;Monsel, Antoine;Qu, Jie-ming;Matthay, Michael A.;Lee, Jae W.
通讯作者:
Lee, Jae W.
影响因子:
3.7
作者:
Bruno S;Grange C;Collino F;Deregibus MC;Cantaluppi V;Biancone L;Tetta C;Camussi G
通讯作者:
Camussi G
影响因子:
1.4
作者:
Guojian Yin;Guoyong Hu;Rong Wan;Ge Yu;Xiaofeng Cang;Jianbo Ni;J. Xiong;Y. Hu;M. Xing;Y. Fan;W. Xiao;Lei Qiu;Shaofeng Wang;Xingpeng Wang
通讯作者:
Guojian Yin;Guoyong Hu;Rong Wan;Ge Yu;Xiaofeng Cang;Jianbo Ni;J. Xiong;Y. Hu;M. Xing;Y. Fan;W. Xiao;Lei Qiu;Shaofeng Wang;Xingpeng Wang
影响因子:
6.1
作者:
Gatti, Stefano;Bruno, Stefania;Camussi, Giovanni
通讯作者:
Camussi, Giovanni