Pleiotropic effects of extracellular vesicles from induced pluripotent stem cell-derived cardiomyocytes on ischemic cardiomyopathy: A preclinical study

被引:5
|
作者
Tominaga, Yuji [1 ]
Kawamura, Takuji [1 ]
Ito, Emiko [1 ]
Takeda, Maki [1 ]
Harada, Akima [1 ]
Torigata, Kosuke [2 ]
Sakaniwa, Ryoto [3 ]
Sawa, Yoshiki [4 ]
Miyagawa, Shigeru [1 ,5 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Cardiovasc Surg, Suita, Osaka, Japan
[2] Osaka Univ, Grad Sch Med, Dept Frontier Regenerat Med, Suita, Osaka, Japan
[3] Osaka Univ, Grad Sch Med, Dept Social Med, Publ Hlth, Suita, Osaka, Japan
[4] Osaka Univ, Grad Sch Med, Dept Future Med, Div Hlth Sci, Suita, Osaka, Japan
[5] Osaka Univ, Grad Sch Med, Dept Cardiovasc Surg, 2-2 Yamada Oka, Suita, Osaka 5650871, Japan
来源
基金
日本学术振兴会;
关键词
myocardial regeneration therapy; ischemic cardiomyopathy; induced pluripotent stem cell-derived cardiomyocytes; extracellular vesicles; M2; macrophage; ENRICHMENT ANALYSIS; HEART-FAILURE; EXOSOMES; FIBROSIS; GENE;
D O I
10.1016/j.healun.2023.08.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Stem cell-secreted extracellular vesicles (EVs) play essential roles in intercellular communication and restore cardiac function in animal models of ischemic heart disease. However, few studies have used EVs derived from clinical-grade stem cells and their derivatives with stable quality. Moreover, there is little information on the mechanism and time course of the multifactorial effect of EV therapy from the acute to the chronic phase, the affected cells, and whether the effects are direct or indirect.METHODS: Induced pluripotent stem cell-derived cardiomyocytes (iPSCM) were produced using a clinical-grade differentiation induction system. EVs were isolated from the conditioned medium by ultracentrifugation and characterized in silico, in vitro, and in vivo. A rat model of myocardial infarction was established by left anterior descending artery ligation and treated with iPSCM-deRESULTS: iPSCM-derived EVs contained microRNAs and proteins associated with angiogenesis, antifibrosis, promotion of M2 macrophage polarization, cell proliferation, and antiapoptosis. iPSCMderived EV treatment improved left ventricular function and reduced mortality in the rat model by improving vascularization and suppressing fibrosis and chronic inflammation in the heart. EVs were uptaken by cardiomyocytes, endothelial cells, fibroblasts, and macrophages in the cardiac tissues. The pleiotropic effects occurred due to the direct effects of microRNAs and proteins encapsulated in EVs and indirect paracrine effects on M2 macrophages. CONCLUSIONS: Clinical-grade iPSCM-derived EVs improve cardiac function by regulating various genes and pathways in various cell types and may have clinical potential for treating ischemic heart disease. J Heart Lung Transplant 2024;43:85-99 (c) 2023 The Authors. Published by Elsevier Inc. on behalf of International Society for Heart and Lung Transplantation. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:85 / 99
页数:15
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