The MRL mouse heart healing response shows donor dominance in allogeneic fetal liver chimeric mice

We previously demonstrated that after a severe cryoinjury to the right ventricle of the heart, adult MRL mice display structural and functional recovery with myocardial tissue replacement resembling that seen in amphibians. The control non-regenerating adult C57BL/6 (B6) mouse shows a predominant sc...

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Veröffentlicht in:Cloning and stem cells 2004, Vol.6 (4), p.352-363
Hauptverfasser: Bedelbaeva, Khamilia, Gourevitch, Dmitri, Clark, Lise, Chen, Pan, Leferovich, John M, Heber-Katz, Ellen
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container_end_page 363
container_issue 4
container_start_page 352
container_title Cloning and stem cells
container_volume 6
creator Bedelbaeva, Khamilia
Gourevitch, Dmitri
Clark, Lise
Chen, Pan
Leferovich, John M
Heber-Katz, Ellen
description We previously demonstrated that after a severe cryoinjury to the right ventricle of the heart, adult MRL mice display structural and functional recovery with myocardial tissue replacement resembling that seen in amphibians. The control non-regenerating adult C57BL/6 (B6) mouse shows a predominant scar response. In the present study, radiation chimeras reconstituted with fetal liver cells from either healer MRL or nonhealer B6 mice were generated to test for a transfer of phenotype. Allogeneic MRL fetal liver cells were injected into x-irradiated (9 Gy) B6 mice and B6 fetal liver cells were injected into x-irradiated MRL mice. In these allogeneic chimeras, the healing response to cardiac cryoinjury was predominantly of the donor phenotype. Thus, MRL fetal liver cells transferred the healing phenotype to the B6 nonhealer with the appearance of Y-chromosome positive, donor-derived cardiomyocytes in the injury site and MRL-like healing with little scar. Similarly, B6 fetal liver cells transferred the nonhealing phenotype to the MRL with little cardiomyocyte growth and an acellular B6-like scar. These results are in contrast to the ear hole closure response which was of the recipient phenotype. We conclude that, in the case of the heart, fetal liver-derived stem cells regulate regenerative healing.
doi_str_mv 10.1089/clo.2004.6.352
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subjects Animals
Cicatrix - physiopathology
Female
Fetus - cytology
Heart Ventricles - injuries
Hepatocytes - physiology
Hepatocytes - transplantation
Mice
Myocytes, Cardiac - physiology
Regeneration - physiology
Regeneration - radiation effects
Transplantation Chimera - physiology
Ventricular Function
Whole-Body Irradiation
title The MRL mouse heart healing response shows donor dominance in allogeneic fetal liver chimeric mice
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