Multimodality Noninvasive Imaging Demonstrates In Vivo Cardiac Regeneration After Mesenchymal Stem Cell Therapy
Luciano C. Amado, MD*, ,
Karl H. Schuleri, MD*, ,
Anastasios P. Saliaris, MD*, ,
Andrew J. Boyle, MBBS, PhD*, ,
Robert Helm, MD*,
Behzad Oskouei, MD*, ,
Marco Centola, MD*, ,
Virginia Eneboe, VT*, ,
Randell Young, MVD ,
Joao A.C. Lima, MD*,
Albert C. Lardo, PhD*,
Alan W. Heldman, MD*, and
Joshua M. Hare, MD*, ,*
* Department of Medicine, Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, Maryland
Institute for Cell Engineering (ICE), Johns Hopkins University School of Medicine, Baltimore, Maryland
OsirisTherapeutics, Baltimore, Maryland

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Figure 1 Multi-detector computed tomography scan of a pig 1 week after myocardial infarction. The different tissue densities of the infarct scar and the sub-endocardial rim of viable tissue are clearly apparent. The sub-endocardial rim has a density similar to the myocardium outside the infarct zone. The relative densities in Hounsfield units (HU) are also represented. MSC = mesenchymal stem cell.
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Figure 2 Multi-detector computed tomography scan of the same mesenchymal stem cell (MSC)-treated animal at 5 days (A), 4 weeks (B), and 8 weeks (C) after MSC injection. There is a time-dependent reduction in the thickness of the infarct scar and a corresponding increase in the thickness of the sub-endocardial rim of tissue over the 8-week follow-up.
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Figure 3 (A) Multi-detector computed tomography scan of representative myocardial infarcts at weeks 1 and 8 after stem cell injection. As indicated by the arrows, both infarct zones are characterized by the presence of a rim of myocardial tissue on their endocardial surface. However, the thickness of this rim progressively increases in mesenchymal stem cell (MSC)-treated animals and remains unchanged in control subjects. (B) Representative pathology specimens from control and MSC-treated animals confirm increased sub-endocardial rim thickness in the treated animals.
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Figure 4 Hematoxylin and eosin (H&E) stain of tissue obtained from the subendocardial rim (A) and the remote zone (B) of mesenchymal stem cell (MSC)-treated animals. As shown, the rim of tissue is made up of cardiomyocytes with normal ultrastructural architecture. (C) There is no difference in the size of myocytes taken from the remote myocardium of both control and MSC hearts. However, the myocytes from the infarct rim are significantly smaller in MSC-treated animals versus control animals (n = 2 each, >100 cells/heart), suggesting that the enhanced rim size in MSC animals might be due to new cardiomyocyte regeneration. *p < 0.001 MSC rim versus control rim.
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Figure 5 Color map depicting non-contractile and dysfunctional areas of myocardium detected by tagging magnetic resonance imaging. Bar color demonstrates the spectrum in change of systolic cardiac function: blue and green colors identify normal contractile areas and red colors represent dysfunctional areas. Non-treated animals exhibited worsening regional systolic function during the 8-week period, whereas a visual improvement was noticed in the mesenchymal stem cell (MSC)-treated animals.
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Figure 7 Impact of mesenchymal stem cell (MSC) therapy on global ventricular function. Ejection fraction assessed by cine magnetic resonance imaging (MRI). Ejection fraction is markedly reduced in both groups at baseline and remains depressed in non-treated animals. However, a progressive improvement in the course of 8 weeks is observed in MSC-treated animals. *p < 0.05 versus day 2 after injection (time 0); p < 0.05 versus non-treated (n = 6).
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