Successful Transplantation of Reduced-Sized Rat Alcoholic Fatty Livers Made Possible by Mobilization of Host Stem Cells
Article first published online: 20 SEP 2012
DOI: 10.1111/j.1600-6143.2012.04265.x
© Copyright 2012 The American Society of Transplantation and the American Society of Transplant Surgeons
Additional Information
How to Cite
Hisada, M., Ota, Y., Zhang, X., Cameron, A. M., Gao, B., Montgomery, R. A., Williams, G. M. and Sun, Z. (2012), Successful Transplantation of Reduced-Sized Rat Alcoholic Fatty Livers Made Possible by Mobilization of Host Stem Cells. American Journal of Transplantation, 12: 3246–3256. doi: 10.1111/j.1600-6143.2012.04265.x
Publication History
- Issue published online: 30 NOV 2012
- Article first published online: 20 SEP 2012
- Received 15 August 2011, revised 23 July 2012 and accepted for publication 24 July 2012
Keywords:
- Fatty liver;
- HGF;
- host stem cells;
- plerixafor;
- reduced sized graft;
- SDF-1
Livers from Lewis rats fed with 7% alcohol for 5 weeks were used for transplantation. Reduced sized (50%) livers or whole livers were transplanted into normal DA recipients, which, in this strain combination, survive indefinitely when the donor has not been fed alcohol. However, none of the rats survived a whole fatty liver transplant while six of seven recipients of reduced sized alcoholic liver grafts survived long term. SDF-1 and HGF were significantly increased in reduced size liver grafts compared to whole liver grafts. Lineage-negative Thy-1+CXCR4+CD133+ stem cells were significantly increased in the peripheral blood and in allografts after reduced size fatty liver transplantation. In contrast, there were meager increases in cells reactive with anti Thy-1, CXCR4 and CD133 in peripheral blood and allografts in whole alcoholic liver recipients. The provision of plerixafor, a stem cell mobilizer, salvaged 5 of 10 whole fatty liver grafts. Conversely, blocking SDF-1 activity with neutralizing antibodies diminished stem cell recruitment and four of five reduced sized fatty liver recipients died. Thus chemokine insufficiency was associated with transplant failure of whole grafts, which was overcome by the increased regenerative requirements promoted by the small grafts and mediated by SDF-1 resulting in stem cell influx.

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