Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2007 Dec;56(12):1725-35.
doi: 10.1136/gut.2007.127969. Epub 2007 Jul 19.

Liver repopulation with bone marrow derived cells improves the metabolic disorder in the Gunn rat

Affiliations

Liver repopulation with bone marrow derived cells improves the metabolic disorder in the Gunn rat

M Muraca et al. Gut. 2007 Dec.

Abstract

Background: Reversible ischaemia/reperfusion (I/R) liver injury has been used to induce engraftment and hepatic parenchymal differentiation of exogenous beta2-microglubulin(-)/Thy1(+) bone marrow derived cells.

Aim: To test the ability of this method of hepatic parenchymal repopulation, theoretically applicable to clinical practice, to correct the metabolic disorder in a rat model of congenital hyperbilirubinaemia.

Methods and results: Analysis by confocal laser microscopy of fluorescence labelled cells and by immunohistochemistry for beta2-microglubulin, 72 hours after intraportal delivery, showed engraftment of infused cells in liver parenchyma of rats with I/R, but not in control animals with non-injured liver. Transplantation of bone marrow derived cells obtained from GFP-transgenic rats into Lewis rats resulted in the presence of up to 20% of GFP positive hepatocytes in I/R liver lobes after one month. The repopulation rate was proportional to the number of transplanted cells. Infusion of GFP negative bone marrow derived cells into GFP positive transgenic rats resulted in the appearance of GFP negative hepatocytes, suggesting that the main mechanism underlying parenchymal repopulation was differentiation rather than cell fusion. Transplantation of wild type bone marrow derived cells into hyperbilirubinaemic Gunn rats with deficient bilirubin conjugation after I/R damage resulted in 30% decrease in serum bilirubin, the appearance of bilirubin conjugates in bile, and the expression of normal UDP-glucuronyltransferase enzyme evaluated by polymerase chain reaction.

Conclusions: I/R injury induced hepatic parenchymal engraftment and differentiation into hepatocyte-like cells of bone marrow derived cells. Transplantation of bone marrow derived cells from non-affected animals resulted in the partial correction of hyperbilirubinaemia in the Gunn rat.

PubMed Disclaimer

Conflict of interest statement

Competing interests: None declared.

References

    1. Lagasse E, Connors H, Al‐Dhalimy M.et al Purified hematopoietic stem cells can differentiate into hepatocytes in vivo. Nat Med 200061229–1234. - PubMed
    1. Wang X, Willenbring H, Akkari Y.et al Cell fusion is the principal source of bone‐marrow‐derived hepatocytes. Nature 2003422897–901. - PubMed
    1. Nussler A, Konigm S, Ott M.et al Present status and perspectives of cell‐based therapies for liver diseases. J Hepatol 200645144–159. - PubMed
    1. Orlic D, Kajstura J, Cimenti S.et al Mobilized bone marrow cells repair the infracted heart, improving function and survival. Proc Natl Acad Sci USA 20019810344–10349. - PMC - PubMed
    1. Gujral J S, Bucci T J, Farhood A.et al Mechanism of cell death during warm hepatic ischemia‐reperfusion in rats: apoptosis or necrosis? Hepatology 200133397–405. - PubMed

Publication types