Bone marrow cells regenerate infarcted myocardium

被引:3915
作者
Orlic, D
Kajstura, J
Chimenti, S
Jakoniuk, I
Anderson, SM
Li, BS
Pickel, J
McKay, R
Nadal-Ginard, B
Bodine, DM
Leri, A
Anversa, P [1 ]
机构
[1] New York Med Coll, Dept Med, Valhalla, NY 10595 USA
[2] NHGRI, Hematopoiesis Sect, Genet & Mol Biol Branch, NIH, Bethesda, MD 20892 USA
[3] NINDS, Mol Biol Lab, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1038/35070587
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Myocardial infarction leads to loss of tissue and impairment of cardiac performance. The remaining myocytes are unable to reconstitute the necrotic tissue, and the post-infarcted heart deteriorates with time(1). Injury to a target organ is sensed by distant stem cells, which migrate to the site of damage and undergo alternate stem cell differentiation(2-5); these events promote structural and functional repair(6-8). This high degree of stem cell plasticity prompted us to test whether dead myocardium could be restored by transplanting bone marrow cells in infarcted mice. We sorted lineage-negative (Lin(-)) bone marrow cells from transgenic mice expressing enhanced green fluorescent protein(9) by fluorescence-activated cell sorting on the basis of c-kit expression(10). Shortly after coronary ligation, Lin(-) c-kit(POS) cells were injected in the contracting wall bordering the infarct. Here we report that newly formed myocardium occupied 68% of the infarcted portion of the ventricle 9 days after transplanting the bone marrow cells. The developing tissue comprised proliferating myocytes and vascular structures. Our studies indicate that locally delivered bone marrow cells can generate de novo myocardium, ameliorating the outcome of coronary artery disease.
引用
收藏
页码:701 / 705
页数:6
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