Immature human engineered heart tissues engraft in a guinea pig chronic injury model

Author:

von Bibra Constantin12ORCID,Shibamiya Aya12,Bähr Andrea34,Geertz Birgit1,Köhne Maria12,Stuedemann Tim12,Starbatty Jutta1,Horneffer-van der Sluis Verena5,Klostermeier Ulrich C.5,Hornaschewitz Nadja34,Li Xinghai6ORCID,Wolf Eckhard7ORCID,Klymiuk Nikolai34,Krane Markus68,Kupatt Christian34,Hiebl Bernhard9,Eschenhagen Thomas12,Weinberger Florian12ORCID

Affiliation:

1. University Medical Center Hamburg-Eppendorf, 20246 Hamburg 1 Department of Experimental Pharmacology and Toxicology , , Germany

2. German Centre for Cardiovascular Research (DZHK) 2 , partner site Hamburg/Kiel/Lübeck , Germany

3. Medizinische Klinik und Poliklinik, University Clinic Rechts der Isar, Technical University Munich 3 , Germany

4. German Centre for Cardiovascular Research (DZHK) 4 , partner site Munich, 80333 München , Germany

5. Institute of Clinical Chemistry and Laboratory Medicine, University Medical Center Hamburg-Eppendorf, 20246 Hamburg 5 , Germany

6. German Heart Centre Munich, Technical University Munich, 80333 München 6 Department of Cardiovascular Surgery , , Germany

7. Gene Center and Center for Innovative Medical Models (CiMM), LMU Munich, 85764 Oberschleißheim 7 , Germany

8. Yale School of Medicine 8 Division of Cardiac Surgery , , New Haven, CT 06510 , USA

9. Institute for Animal Hygiene, Animal Welfare and Farm Animal Behaviour, University of Veterinary Medicine Hannover 9 , 30559 Hannover , Germany

Abstract

ABSTRACT Engineered heart tissue (EHT) transplantation represents an innovative, regenerative approach for heart failure patients. Late preclinical trials are underway, and a first clinical trial started recently. Preceding studies revealed functional recovery after implantation of in vitro-matured EHT in the subacute stage, whereas transplantation in a chronic injury setting was less efficient. When transplanting matured EHTs, we noticed that cardiomyocytes undergo a dedifferentiation step before eventually forming structured grafts. Therefore, we wanted to evaluate whether immature EHT (EHTIm) patches can be used for transplantation. Chronic myocardial injury was induced in a guinea pig model. EHTIm (15×106 cells) were transplanted within hours after casting. Cryo-injury led to large transmural scars amounting to 26% of the left ventricle. Grafts remuscularized 9% of the scar area on average. Echocardiographic analysis showed some evidence of improvement of left-ventricular function after EHTIm transplantation. In a small translational proof-of-concept study, human scale EHTIm patches (4.5×108 cells) were epicardially implanted on healthy pig hearts (n=2). In summary, we provide evidence that transplantation of EHTIm patches, i.e. without precultivation, is feasible, with similar engraftment results to those obtained using matured EHT.

Funder

Deutsches Zentrum für Herz-Kreislaufforschung

European Research Council

Deutsche Forschungsgemeinschaft

Horizon 2020

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

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