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TISSUE-SPECIFIC STEM CELLS

Bone Marrow Cells Transdifferentiate to Cardiomyocytes When Introduced into the Embryonic Heart

^a Department of Cell Biology and Anatomy, Medical University of South Carolina, Charleston, South Carolina, USA;
^b Cell Developmental Biology Program, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA

Key Words. Cardiac • Myocardium • Transdifferentiation • Stem cells • Bone marrow • Macrophages

Correspondence: Leonard M. Eisenberg, Ph.D., Medical University of South Carolina, Department of Cell Biology and Anatomy, BSB Room 654,171 Ashley Ave., Charleston, South Carolina 29425, USA. Telephone: 843-792-9844; Fax: 843-792-0664; e-mail: eisenblm{at}musc.edu

Received March 22, 2005; accepted for publication January 1, 2006.
Since rates of cardiomyocyte generation in the embryo are much higher than within the adult, we explored whether the embryonic heart would serve as useful experimental system for examining the myocardial potential of adult stem cells. Previously, we reported that the long-term culturing of adult mouse bone marrow produced a cell population that was both highly enriched for macrophages and cardiac competent. In this study, the myocardial potential of this cell population was analyzed in greater detail using the embryonic chick heart as recipient tissue. Experiments involving the co-incubation of labeled bone marrow cells with embryonic heart tissue showed that bone marrow (BM) cells incorporated into the myocardium and immunostained for myocyte proteins. Reverse transcription-polymerase chain reaction analysis demonstrated that the heart tissue induced bone marrow cells to express the differentiated cardiomyocyte marker -cardiac myosin heavy chain. The cardiomyocyte conversion of the bone marrow cells was verified by harvesting donor cells from mice that were genetically labeled with a myocardial-specific ß-galactosidase reporter. Embryonic hearts exposed to the transgenic bone marrow in culture exhibited significant numbers of ß-galactosidase-positive cells, indicating the presence of bone marrow-derived cells that had converted to a myocardial phenotype. Furthermore, when transgenic mouse BM cells were injected into living chick embryos, donor cells incorporated into the developing heart and exhibited a myocardial phenotype. Immunofluorescence analysis demonstrated that donor BM cells exhibiting myocyte markers contained only nuclei from mouse cells, indicating that differentiation and not cell fusion was the predominant mechanism for the acquisition of a myocyte phenotype. These data confirm that adult mouse bone marrow contain cells with the ability to form cardiomyocytes. In addition, the predominance of the macrophage phenotype within the donor bone marrow cell population suggests that transdifferentiation of immune response cells may play a role in cellular regeneration in the adult.

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