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Human umbilical cord mesenchymal stromal cells rescue mice from acetaminophen-induced acute liver failure.

Authors :
ZONGCAI LIU
FANWEI MENG
CHAN LI
XIN ZHOU
XIAOPING ZENG
YIXIN HE
MRSNY, RANDALL J.
MUYUN LIU
XIANG HU
JI-FAN HU
TAO LI
Source :
Cytotherapy (Elsevier Inc.). Sep2014, Vol. 16 Issue 9, p1207-1219. 13p.
Publication Year :
2014

Abstract

Background aims. Acute liver failure (ALF), a life-threatening disease characterized by the sudden loss of hepatic function, can occur after an accidental or intentional acetaminophen overdose. Methods. With the use of an ALF mouse model, we examined both the preventive and therapeutic potential of intravenously administered human umbilical cord-derived mesenchymal stromal cells (hUCMSCs). Primary hUCMSCs were purified from freshly collected full-term umbilical cords and intravenously transplanted into BALB/c mice either before and after ALF induced by acetaminophen intoxication. We found that hUCMSCs significantly improved survival rates and relative liver weight of mice in both pre-ALF and post-ALF animals. Correspondingly, serum levels of markers that reflect hepatic injury (ie, aspartate aminotransferase, alanine aminotransferase and total bilirubin) were significantly attenuated in the group receiving hUCMSC therapy Results Mechanistically, we found that the protective potential of intravenously administered hUCMSCs was mediated by paracrine pathways that involved antioxidants (glutathione, superoxide dismutase), the reduction of inflammatory agents (tumor necrosis factor-a, mterleukin-6) and elevated serum levels of hepatocyte growth factor. Conclusions. Through these paracrine effects, intravenously administered hUCMSCs reduced hepatic necrosis/apoptosis and enhanced liver regeneration Thus our data demonstrate that intravenously administered hUCMSCs may be useful in the prevention or treatment of acetaminophen- induced ALF. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14653249
Volume :
16
Issue :
9
Database :
Academic Search Index
Journal :
Cytotherapy (Elsevier Inc.)
Publication Type :
Academic Journal
Accession number :
97600590
Full Text :
https://doi.org/10.1016/j.jcyt.2014.05.018