Mesenchymal progenitor cells differentiate into an endothelial phenotype, enhance vascular density, and improve heart function in a rat cellular cardiomyoplasty model

• Published in: Circulation (New York, N.Y.) N.Y.), 2003-09, Vol.108 (10), p.253-258
• Main Authors: DAVANI, Siamak, MARANDIN, Aliette, MERSIN, Nursen, ROYER, Bernard, KANTELIP, Bernadette, HERVE, Patrick, ETIEVENT, Joseph-Philippe, KANTELIP, Jean-Pierre
• Format: Article
• Language: English
• Subjects: Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Animals; Applied cell therapy and gene therapy; Biological and medical sciences; Bone Marrow Cells - cytology; Cell Differentiation; Cells, Cultured; Coronary Vessels - pathology; Endothelium, Vascular - cytology; Male; Medical sciences; Mesoderm - cytology; Myocardial Infarction - diagnostic imaging; Myocardial Infarction - pathology; Myocardial Infarction - therapy; Phenotype; Rats; Rats, Inbred Lew; Stem Cell Transplantation; Stem Cells - cytology; Stem Cells - physiology; Transfusions. Complications. Transfusion reactions. Cell and gene therapy; Ultrasonography; Ventricular Function, Left
• ISSN: 0009-7322; 1524-4539
• DOI: 10.1161/01.cir.0000089186.09692.fa

Cellular cardiomyoplasty is a promising approach to improve postinfarcted cardiac function. The differentiation pathways of engrafted mesenchymal progenitor cells (MPCs) and their effects on the left ventricular function in a rat myocardial infarct heart model were analyzed. A ligation model of left coronary artery of Lewis rats was used. MPCs were isolated by bone marrow cell adherence. Seven days after ligation, MPCs labeled with 4',6-diamidino-2'-phenylindole were injected into the infarcted myocardium (n=8). Culture medium was injected in the infarcted myocardium of control animals (n=8). Thirty days after implantation, immunofluorescence studies revealed some engrafted cells expressing a smooth muscle phenotype (alpha SM actin+), as similarly observed in culture. Other engrafted cells lost their smooth muscle phenotype and acquired an endothelial phenotype (CD31+). Furthermore, vessel density was augmented in the MPC group in comparison with the control group. After 30 days, echocardiography showed an improvement on left ventricular performance in the MPCs compared with the control group. In vivo administration of syngenic MPCs into a rat model of myocardial infarcted heart was safety demonstrated. Some engrafted cells appeared to differentiate into endothelial cells and loss their smooth muscle phenotype. MPC engraftment might to contribute to the improvement on the cardiac function in such a setting.