Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention
Abstract Myocardial fibrosis and ventricular remodeling were the key pathology factors causing undesirable consequence after myocardial infarction. However, an efficient therapeutic method remains unclear, partly due to difficulty in continuously preventing neurohormonal overactivation and potential...
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Nature Portfolio
2021
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oai:doaj.org-article:e774ffa4f866423787236636797b8e4a2021-12-02T16:27:51ZMyocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention10.1038/s41536-021-00154-y2057-3995https://doaj.org/article/e774ffa4f866423787236636797b8e4a2021-08-01T00:00:00Zhttps://doi.org/10.1038/s41536-021-00154-yhttps://doaj.org/toc/2057-3995Abstract Myocardial fibrosis and ventricular remodeling were the key pathology factors causing undesirable consequence after myocardial infarction. However, an efficient therapeutic method remains unclear, partly due to difficulty in continuously preventing neurohormonal overactivation and potential disadvantages of cell therapy for clinical practice. In this study, a rhACE2-electrospun fibrous patch with sustained releasing of rhACE2 to shape an induction transformation niche in situ was introduced, through micro-sol electrospinning technologies. A durable releasing pattern of rhACE2 encapsulated in hyaluronic acid (HA)—poly(L-lactic acid) (PLLA) core-shell structure was observed. By multiple in vitro studies, the rhACE2 patch demonstrated effectiveness in reducing cardiomyocytes apoptosis under hypoxia stress and inhibiting cardiac fibroblasts proliferation, which gave evidence for its in vivo efficacy. For striking mice myocardial infarction experiments, a successful prevention of adverse ventricular remodeling has been demonstrated, reflecting by improved ejection fraction, normal ventricle structure and less fibrosis. The rhACE2 patch niche showed clear superiority in long term function and structure preservation after ischemia compared with intramyocardial injection. Thus, the micro-sol electrospun rhACE2 fibrous patch niche was proved to be efficient, cost-effective and easy-to-use in preventing ventricular adverse remodeling.Zeping QiuJingwen ZhaoFanyi HuangLuhan BaoYanjia ChenKe YangWenguo CuiWei JinNature PortfolioarticleMedicineRENnpj Regenerative Medicine, Vol 6, Iss 1, Pp 1-12 (2021) |
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Medicine R Zeping Qiu Jingwen Zhao Fanyi Huang Luhan Bao Yanjia Chen Ke Yang Wenguo Cui Wei Jin Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
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Abstract Myocardial fibrosis and ventricular remodeling were the key pathology factors causing undesirable consequence after myocardial infarction. However, an efficient therapeutic method remains unclear, partly due to difficulty in continuously preventing neurohormonal overactivation and potential disadvantages of cell therapy for clinical practice. In this study, a rhACE2-electrospun fibrous patch with sustained releasing of rhACE2 to shape an induction transformation niche in situ was introduced, through micro-sol electrospinning technologies. A durable releasing pattern of rhACE2 encapsulated in hyaluronic acid (HA)—poly(L-lactic acid) (PLLA) core-shell structure was observed. By multiple in vitro studies, the rhACE2 patch demonstrated effectiveness in reducing cardiomyocytes apoptosis under hypoxia stress and inhibiting cardiac fibroblasts proliferation, which gave evidence for its in vivo efficacy. For striking mice myocardial infarction experiments, a successful prevention of adverse ventricular remodeling has been demonstrated, reflecting by improved ejection fraction, normal ventricle structure and less fibrosis. The rhACE2 patch niche showed clear superiority in long term function and structure preservation after ischemia compared with intramyocardial injection. Thus, the micro-sol electrospun rhACE2 fibrous patch niche was proved to be efficient, cost-effective and easy-to-use in preventing ventricular adverse remodeling. |
format |
article |
author |
Zeping Qiu Jingwen Zhao Fanyi Huang Luhan Bao Yanjia Chen Ke Yang Wenguo Cui Wei Jin |
author_facet |
Zeping Qiu Jingwen Zhao Fanyi Huang Luhan Bao Yanjia Chen Ke Yang Wenguo Cui Wei Jin |
author_sort |
Zeping Qiu |
title |
Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
title_short |
Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
title_full |
Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
title_fullStr |
Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
title_full_unstemmed |
Myocardial fibrosis reversion via rhACE2-electrospun fibrous patch for ventricular remodeling prevention |
title_sort |
myocardial fibrosis reversion via rhace2-electrospun fibrous patch for ventricular remodeling prevention |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/e774ffa4f866423787236636797b8e4a |
work_keys_str_mv |
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