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Circulation. 2002;106:2-4
doi: 10.1161/01.CIR.0000024386.99599.4A
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(Circulation. 2002;106:2.)
© 2002 American Heart Association, Inc.


Editorial

Cardiac Chimerism as a Mechanism for Self-Repair

Does It Happen and If So to What Degree?

Doris A. Taylor, PhD; Ralph Hruban, MD; E.Rene Rodriguez, MD; Pascal J. Goldschmidt-Clermont, MD

From the Division of Cardiology (D.A.T., P.J.G.) Duke University Medical Center, Durham, NC; and the Department of Pathology (R.H., E.R.R.), Johns Hopkins University School of Medicine, Baltimore, Md.

Correspondence to Doris A. Taylor, PhD, Associate Professor, Division of Cardiology, Box 3345 DUMC, Duke University Medical Center, Durham, NC 27710. E-mail dataylor@duke.edu


Key Words: Editorials • myocytes • transplantation • regeneration • cells


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

Cardiac regeneration is an area that has gained considerable attention lately, especially with the finding that immature muscle cells and/or autologous stem cells can regenerate function in a previously injured heart.1,2,3 However, this fertile field remains unsettled enough that each piece of new data should be rigorously scrutinized. Toward that end, a controversy has arisen recently concerning the potential for cardiovascular self-repair evidenced by chimerism in an allografted human heart. Several investigators have allografted female hearts into human male recipients and examined the heart at the time of explantation for the presence of Y chromosome–positive cells either in the coronary vasculature or within cardiomyocytes.4–7 Conflicting results have been obtained. The report by Glaser et al4 in this issue of Circulation presents one side of the controversy, namely that regeneration is possible to a certain degree in the coronary vasculature but fails to occur within cardiomyocytes.4 In contrast, the recent report by Quaini et al5 claimed not only that vascular regeneration occurs, but also that repair of up to 30% of the donor myocardium takes place within 1 month of transplantation.

See p 17

The notion of progenitor cell–based vascular repair arises naturally from our understanding of vascular biology, where endothelial and smooth muscle cell turnover and replacement are clinically accepted. In fact, the use of endothelial progenitor cells to repair damaged vasculature is an exciting new area of investigation.8

In contrast, the controversy over myocardial chimerism and repair is one that requires a paradigm shift from the accepted dogma of . . . [Full Text of this Article]




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