期刊
出版社
ELSEVIER
DOI: 10.1016/j.msec.2020.111539
关键词
Hydrogel; Injectable; Peptide; Self-assembly; Cardiac repair; Cell culture
资金
- European Union Framework Programme 7 (BIOSCENT) [214539]
- UK Engineering and Physical Sciences Research Council [EP/K016210/1]
- European Cooperation in Science and Technology [16122-BIONECA]
- British Heart Foundation [nPG/17/78/33304]
- EPSRC [EP/K016210/1] Funding Source: UKRI
- MRC [MR/P015816/1] Funding Source: UKRI
Heart failure is a leading cause of death worldwide, often developing after myocardial infarction. The limited regenerative capacity of the heart, due to the characteristic of adult cardiomyocytes, necessitates the development of novel cell-based therapies. Using a self-assembling peptide hydrogel as scaffold for delivering cardiac progenitor cells has shown promising results in promoting heart regeneration.
Heart failure (HF) remains one of the leading causes of death worldwide; most commonly developing after myocardial infarction (MI). Since adult cardiomyocytes characteristically do not proliferate, cells lost during MI are not replaced. As a result, the heart has a limited regenerative capacity. There is, therefore, a need to develop novel cell-based therapies to promote the regeneration of the heart after MI. The delivery and retention of cells at the injury site remains a significant challenge. In this context, we explored the potential of using an injectable, RGDSP-functionalised self-assembling peptide - FEFEFKFK - hydrogel as scaffold for the delivery and retention of rat cardiac progenitor cells (CPCs) into the heart. Our results show that culturing CPCs in vitro within the hydrogel for one-week promoted their spontaneous differentiation towards adult cardiac phenotypes. Injection of the hydrogel on its own, or loaded with CPCs, into the rat after injury resulted in a significant reduction in myocardial damage and left ventricular dilation.
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