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

被引:16
作者
Bedelbaeva, K [1 ]
Gourevitch, D [1 ]
Clark, L [1 ]
Chen, P [1 ]
Leferovich, JM [1 ]
Heber-Katz, E [1 ]
机构
[1] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
关键词
D O I
10.1089/clo.2004.6.352
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 northealing 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.
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页码:352 / 363
页数:12
相关论文
共 61 条
[1]   Ventricular myocytes are not terminally differentiated in the adult mammalian heart [J].
Anversa, P ;
Kajstura, J .
CIRCULATION RESEARCH, 1998, 83 (01) :1-14
[2]  
ARMAND O, 1983, ARCH ANAT MICROSC MO, V72, P163
[3]   Haematopoietic stem cells adopt mature haematopoietic fates in ischaemic myocardium [J].
Balsam, LB ;
Wagers, AJ ;
Christensen, JL ;
Kofidis, T ;
Weissman, IL ;
Robbins, RC .
NATURE, 2004, 428 (6983) :668-673
[4]   Evidence that human cardiac myocytes divide after myocardial infarction (Publication with Expression of Concern. See vol. 379, pg. 1870, 2018) [J].
Beltrami, AP ;
Urbanek, K ;
Kajstura, J ;
Yan, SM ;
Finato, N ;
Bussani, R ;
Nadal-Ginard, B ;
Silvestri, F ;
Leri, A ;
Beltrami, CA ;
Anversa, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (23) :1750-1757
[5]   Adult cardiac stem cells are multipotent and support myocardial regeneration [J].
Beltrami, AP ;
Barlucchi, L ;
Torella, D ;
Baker, M ;
Limana, F ;
Chimenti, S ;
Kasahara, H ;
Rota, M ;
Musso, E ;
Urbanek, K ;
Leri, A ;
Kajstura, J ;
Nadal-Ginard, B ;
Anversa, P .
CELL, 2003, 114 (06) :763-776
[6]  
BISCHOFF R, 1994, MYOGENESIS, V2, P97
[7]   Turning brain into blood: A hematopoietic fate adopted by adult neural stem cells in vivo [J].
Bjornson, CRR ;
Rietze, RL ;
Reynolds, BA ;
Magli, MC ;
Vescovi, AL .
SCIENCE, 1999, 283 (5401) :534-537
[8]   Sexually dimorphic genes regulate healing and regeneration in MRL mice [J].
Blankenhorn, EP ;
Troutman, S ;
Clark, LD ;
Zhang, XM ;
Chen, P ;
Heber-Katz, E .
MAMMALIAN GENOME, 2003, 14 (04) :250-260
[9]  
CARBONE A, 1995, ANN NY ACAD SCI, V752, P75
[10]   A new murine model for mammalian wound repair and regeneration [J].
Clark, LD ;
Clark, RK ;
Heber-Katz, E .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 88 (01) :35-45