Three-dimensional heart extracellular matrix enhances chemically induced direct cardiac reprogramming

Author:

Jin Yoonhee12ORCID,Kim Hyeok34ORCID,Min Sungjin1ORCID,Choi Yi Sun1ORCID,Seo Seung Ju2ORCID,Jeong Eunseon1ORCID,Kim Su Kyeom1,Lee Hyang-Ae5ORCID,Jo Sung-Hyun6ORCID,Park Jae-Hyun34ORCID,Park Bong-Woo34ORCID,Sim Woo-Sup34ORCID,Kim Jin-Ju34ORCID,Ban Kiwon7ORCID,Kim Yun-Gon6ORCID,Park Hun-Jun348ORCID,Cho Seung-Woo1910ORCID

Affiliation:

1. Department of Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.

2. Department of Physiology, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.

3. Department of Biomedicine and Health Sciences, The Catholic University of Korea, Seoul 06591, Republic of Korea.

4. Division of Cardiology, Department of Internal Medicine, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seoul 06591, Republic of Korea.

5. Korea Institute of Toxicology, Korea Research Institute of Chemical Technology, Daejeon 34114, Republic of Korea.

6. Department of Chemical Engineering, Soongsil University, Seoul 06978, Republic of Korea.

7. Department of Biomedical Sciences, City University of Hong Kong, Kowloon 999077, Hong Kong.

8. Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.

9. Center for Nanomedicine, Institute for Basic Science (IBS), Seoul 03722, Republic of Korea.

10. Graduate Program of Nano Biomedical Engineering (NanoBME), Advanced Science Institute, Yonsei University, Seoul 03722, Republic of Korea.

Abstract

Direct cardiac reprogramming has emerged as a promising therapeutic approach for cardiac regeneration. Full chemical reprogramming with small molecules to generate cardiomyocytes may be more amenable than genetic reprogramming for clinical applications as it avoids safety concerns associated with genetic manipulations. However, challenges remain regarding low conversion efficiency and incomplete cardiomyocyte maturation. Furthermore, the therapeutic potential of chemically induced cardiomyocytes (CiCMs) has not been investigated. Here, we report that a three-dimensional microenvironment reconstituted with decellularized heart extracellular matrix can enhance chemical reprogramming and cardiac maturation of fibroblasts to cardiomyocytes. The resultant CiCMs exhibit elevated cardiac marker expression, sarcomeric organization, and improved electrophysiological features and drug responses. We investigated the therapeutic potential of CiCMs reprogrammed in three-dimensional heart extracellular matrix in a rat model of myocardial infarction. Our platform can facilitate the use of CiCMs for regenerative medicine, disease modeling, and drug screening.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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