» Articles » PMID: 32269164

An Off-the-shelf Artificial Cardiac Patch Improves Cardiac Repair After Myocardial Infarction in Rats and Pigs

Overview
Journal Sci Transl Med
Date 2020 Apr 10
PMID 32269164
Citations 76
Authors
Affiliations
Soon will be listed here.
Abstract

Cell therapy has been a promising strategy for cardiac repair after injury or infarction; however, low retention and engraftment of transplanted cells limit potential therapeutic efficacy. Seeding scaffold material with cells to create cardiac patches that are transplanted onto the surface of the heart can overcome these limitations. However, because patches need to be freshly prepared to maintain cell viability, long-term storage is not feasible and limits clinical applicability. Here, we developed an off-the-shelf therapeutic cardiac patch composed of a decellularized porcine myocardial extracellular matrix scaffold and synthetic cardiac stromal cells (synCSCs) generated by encapsulating secreted factors from isolated human cardiac stromal cells. This fully acellular artificial cardiac patch (artCP) maintained its potency after long-term cryopreservation. In a rat model of acute myocardial infarction, transplantation of the artCP supported cardiac recovery by reducing scarring, promoting angiomyogenesis, and boosting cardiac function. The safety and efficacy of the artCP were further confirmed in a porcine model of myocardial infarction. The artCP is a clinically feasible, easy-to-store, and cell-free alternative to myocardial repair using cell-based cardiac patches.

Citing Articles

Microneedle patches: the next frontier in cardiovascular care.

Kaur S, Choudhary S, Sen S, Pemmaraju D, Singh S, Kapoor D Drug Deliv Transl Res. 2025; .

PMID: 39881106 DOI: 10.1007/s13346-025-01802-2.


Small Extracellular Vesicles Isolated from Cardiac Tissue Matrix or Plasma Display Distinct Aging-Related Changes in Cargo Contributing to Chronic Cardiovascular Disease.

Ronan G, Yang J, Zorlutuna P bioRxiv. 2024; .

PMID: 39713371 PMC: 11661072. DOI: 10.1101/2024.12.06.627231.


A Heart Rate Matched Patch for Mechano-Chemical Treatment of Myocardial Infarction: Optimal Design and Transspecies Application.

Jia Y, Wei Z, Feng J, Lei M, Yang Y, Liu J Research (Wash D C). 2024; 7:0517.

PMID: 39582687 PMC: 11582187. DOI: 10.34133/research.0517.


Orbit symmetry breaking in MXene implements enhanced soft bioelectronic implants.

Wu Y, Li Y, Liu Y, Zhu D, Xing S, Lambert N Sci Adv. 2024; 10(40):eadp8866.

PMID: 39356763 PMC: 11446273. DOI: 10.1126/sciadv.adp8866.


Application of Pro-angiogenic Biomaterials in Myocardial Infarction.

Liang T, Liu J, Liu F, Su X, Li X, Zeng J ACS Omega. 2024; 9(36):37505-37529.

PMID: 39281944 PMC: 11391569. DOI: 10.1021/acsomega.4c04682.


References
1.
Park S, Kim R, Park B, Lee S, Choi S, Park J . Dual stem cell therapy synergistically improves cardiac function and vascular regeneration following myocardial infarction. Nat Commun. 2019; 10(1):3123. PMC: 6635499. DOI: 10.1038/s41467-019-11091-2. View

2.
Bassat E, Eid Mutlak Y, Genzelinakh A, Shadrin I, Umansky K, Yifa O . The extracellular matrix protein agrin promotes heart regeneration in mice. Nature. 2017; 547(7662):179-184. PMC: 5769930. DOI: 10.1038/nature22978. View

3.
Sharp 3rd T, Schena G, Hobby A, Starosta T, Berretta R, Wallner M . Cortical Bone Stem Cell Therapy Preserves Cardiac Structure and Function After Myocardial Infarction. Circ Res. 2017; 121(11):1263-1278. PMC: 5681384. DOI: 10.1161/CIRCRESAHA.117.311174. View

4.
Shen D, Tang J, Hensley M, Li T, Caranasos T, Zhang T . Effects of Matrix Metalloproteinases on the Performance of Platelet Fibrin Gel Spiked With Cardiac Stem Cells in Heart Repair. Stem Cells Transl Med. 2016; 5(6):793-803. PMC: 4878332. DOI: 10.5966/sctm.2015-0194. View

5.
Hodgkinson C, Bareja A, Gomez J, Dzau V . Emerging Concepts in Paracrine Mechanisms in Regenerative Cardiovascular Medicine and Biology. Circ Res. 2016; 118(1):95-107. PMC: 4874329. DOI: 10.1161/CIRCRESAHA.115.305373. View