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J Am Coll Cardiol, 2004; 44:458-463, doi:10.1016/j.jacc.2004.03.083
© 2004 by the American College of Cardiology Foundation
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Comparison of human skeletal myoblasts and bone marrow-derived CD133+ progenitors for the repair of infarcted myocardium

Onnik Agbulut, PhD*{dagger},*, Susanne Vandervelde*, Nawwar Al Attar, MD*{dagger}, Jérôme Larghero, MD{ddagger}{ddagger}, Said Ghostine, MD{dagger}§, Bertrand Léobon, MD||||, Estelle Robidel*, Paolo Borsani, MD*, Marc Le Lorc'h¶¶, Alvine Bissery, PhD||, Christine Chomienne, MD, PhD{dagger}{dagger}, Patrick Bruneval, MD, PhD¶#, Jean-Pierre Marolleau, MD{ddagger}{ddagger}, Jean-Thomas Vilquin, PhD§§, Albert Hagège, MD, PhD§, Jane-Lyse Samuel, PhD* and Philippe Menasché, MD, PhD{dagger}**

* Inserm U572, Hôpital Lariboisiére, Paris, France
{dagger} Inserm U633, Hôpital Européen Georges Pompidou, Paris, France
§ Department of Cardiology, Hôpital Européen Georges Pompidou, Paris, France
|| Clinical Investigation Center 9201, Hôpital Européen Georges Pompidou, Paris, France
Department of Pathology, Hôpital Européen Georges Pompidou, Paris, France
# Inserm U430, Hôpital Européen Georges Pompidou, Paris, France
** Department of Cardiovascular Surgery, Hôpital Européen Georges PompidouParis, France
{dagger}{dagger} Inserm E0003, Paris, France
{ddagger}{ddagger} Laboratory of Cell Therapy, Hôpital Saint-LouisParis, France
§§ Inserm U582, Paris, France
|||| Assistance Publique-Hôpitaux de Paris, Ecole de Chirurgie; Paris, France
¶¶ Department of Cytogenetics, Hôpital Necker, Paris, France



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Figure 1 Functional effects of CD133+ and skeletal myoblast (SM) cell transplantation. (A) Individual values and mean percentage of change in left ventricular ejection fraction (LVEF) from baseline pretransplantation values in controls (n = 9; open triangles), CD133+-treated (n = 15; closed circles), and SM-treated (n = 8; closed triangles) hearts. (B) Representative tracings of pressure-volume occlusion loops. (C and D) Individual values and means of (C) maximal elastance (Emax) and (D) preload-recruitable stroke work (PRSW) in controls (n = 9), CD133+-grafted (n = 12), and SM-grafted (n = 7) hearts. Note the functional improvement in >25% of CD133+-grafted and SM-grafted animals.*p = 0.0015, {dagger}p = 0.008, {ddagger}p = 0.01 vs. controls.

 


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Figure 2 Detection of human cells in grafted rat hearts. One month after skeletal myoblast (SM) grafting, immunofluorescence shows that many cells were positively stained for human lamins-A/C (A); some of them expressed (B) neonatal myosin heavy chain (MyHC) (arrows) and (C) adult-fast MyHC. (D) Detection via polymerase chain reaction of human cells in grafted hearts using a human-specific Alu primer.

 




 
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