Projects per year
Abstract
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.
Original language | English |
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Journal | Materials Science and Engineering: C |
Publication status | Accepted/In press - 16 Sept 2020 |
Research Beacons, Institutes and Platforms
- Manchester Institute of Biotechnology
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- 1 Finished
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Targeting the Hippo Pathway to Enhance the Regenerative Capacity of IPS-Derived Cardiomyocyte.
Oceandy, D. (PI) & Cartwright, E. (CoI)
1/04/18 → 31/03/21
Project: Research