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    Human adipose-derived mesenchymal stem cells attenuate liver ischemia-reperfusion injury and promote liver regeneration

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    Authors
    Saidi, Reza F.
    Rajeshkumar, Barur R.
    Shariftabrizi, Ahmad
    Bogdanov, Alexei A. Jr.
    Zheng, Shaokuan
    Dresser, Karen A.
    Walter, Otto
    UMass Chan Affiliations
    Department of Radiology
    Department of Pathology
    Department of Medicine
    Document Type
    Journal Article
    Publication Date
    2014-11-01
    Keywords
    Pathology
    Radiology
    Surgery
    
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    Link to Full Text
    https://doi.org/10.1016/j.surg.2014.05.008
    Abstract
    BACKGROUND: Ischemia-reperfusion injury (IRI) of the liver is a well-known cause of morbidity and mortality after liver transplantation. Effective treatment strategies aimed at decreasing hepatic IRI injury and accelerating liver regeneration could offer major benefits in liver transplantation, especially in the case of partial allografts. Human adipose-derived mesenchymal stem cells (HADMSCs) are an attractive source for regenerative medicine because of their anti-inflammatory and regenerative properties. We hypothesized that HADMSCs attenuate IRI and promote liver regeneration. METHODS: Mice were subjected to 60 minutes of partial IRI with or without 70% partial hepatectomy. Animals were treated with HADMSCs. Liver IRI was evaluated with serum levels of alanine aminotransferase, serum interleukin-6, and histopathology. Liver samples were stained for specific markers of liver regeneration. RESULTS: Histology, serum interleukin-6, and alanine aminotransferase release revealed that treatment with HADMSCs attenuated liver injury compared with control patients. Improved animal survival and increased number of regenerating cells were observed in HADMSC-treated animals who underwent IRI and partial hepatectomy compared with the control group. CONCLUSION: HADMSC represents a potential therapeutic strategy to decrease IRI and promote regeneration in liver transplantation.
    Source
    Surgery. 2014 Nov;156(5):1225-31. Epub 2014 Sep26. Link to article on publisher's site
    DOI
    10.1016/j.surg.2014.05.008
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/48156
    PubMed ID
    25262218
    Related Resources
    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.surg.2014.05.008
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