Composite Cell Sheets

Author:

Bel Alain1,Planat-Bernard Valérie1,Saito Atsuhiro1,Bonnevie Lionel1,Bellamy Valérie1,Sabbah Laurent1,Bellabas Linda1,Brinon Benjamin1,Vanneaux Valérie1,Pradeau Pascal1,Peyrard Séverine1,Larghero Jérôme1,Pouly Julia1,Binder Patrice1,Garcia Sylvie1,Shimizu Tatsuya1,Sawa Yoshiki1,Okano Teruo1,Bruneval Patrick1,Desnos Michel1,Hagège Albert A.1,Casteilla Louis1,Pucéat Michel1,Menasché Philippe1

Affiliation:

1. From the Assistance Publique-Hôpitaux de Paris (A.B., J.P., P.M.), Hôpital Européen Georges Pompidou, Department of Cardiovascular Surgery; University Paris Descartes; INSERM U633, Laboratory of Biosurgical Research, Paris, France; University of Toulouse (V.P.-B., L.C.), UPS, CNRS, UMR 5241 Métabolisme, Plasticité et Mitochondrie, Toulouse, France; Medical Center for Translational Research (A.S., Y.S.), Osaka University Hospital, Osaka, Japan; Hôpital d’Instruction des Armées Bégin (L.B.),...

Abstract

Background— The safety and efficacy of myocardial regeneration using embryonic stem cells are limited by the risk of teratoma and the high rate of cell death. Methods and Results— To address these issues, we developed a composite construct made of a sheet of adipose tissue–derived stroma cells and embryonic stem cell–derived cardiac progenitors. Ten Rhesus monkeys underwent a transient coronary artery occlusion followed, 2 weeks later, by the open-chest delivery of the composite cell sheet over the infarcted area or a sham operation. The sheet was made of adipose tissue–derived stroma cells grown from a biopsy of autologous adipose tissue and cultured onto temperature-responsive dishes. Allogeneic Rhesus embryonic stem cells were committed to a cardiac lineage and immunomagnetically sorted to yield SSEA-1 + cardiac progenitors, which were then deposited onto the cell sheet. Cyclosporine was given for 2 months until the animals were euthanized. Preimplantation studies showed that the SSEA-1 + progenitors expressed cardiac markers and had lost pluripotency. After 2 months, there was no teratoma in any of the 5 cell-treated monkeys. Analysis of >1500 histological sections showed that the SSEA-1 + cardiac progenitors had differentiated into cardiomyocytes, as evidenced by immunofluorescence and real-time polymerase chain reaction. There were also a robust engraftment of autologous adipose tissue–derived stroma cells and increased angiogenesis compared with the sham animals. Conclusions— These data collected in a clinically relevant nonhuman primate model show that developmentally restricted SSEA-1 + cardiac progenitors appear to be safe and highlight the benefit of the epicardial delivery of a construct harboring cells with a cardiomyogenic differentiation potential and cells providing them the necessary trophic support.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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