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光生物调节驱动 miR-136-5p 的表达,促进心肌梗死后的损伤修复。

Photobiomodulation Drives MiR-136-5p Expression to Promote Injury Repair after Myocardial Infarction.

机构信息

Department of Laboratory Medicine at the Fourth Affiliated Hospital, and Department of Pharmacy at the Second Affiliated Hospital, Harbin Medical University, Harbin, China.

Department of Pharmacology (State-Province Key Laboratories of Biomedicine-Pharmaceutics of China, Key Laboratory of Cardiovascular Research, Ministry of Education) at College of Pharmacy, Harbin Medical University, Harbin, China.

出版信息

Int J Biol Sci. 2022 Apr 18;18(7):2980-2993. doi: 10.7150/ijbs.71440. eCollection 2022.

Abstract

Photobiomodulation (PBM) has emerged as an alternative therapy involved in modulating a variety of biological effects. In this study, we verified whether PBM can affect cardiac physiological activity in mice through noninvasive irradiation using light-emitting diodes at a wavelength of 630 nm (LED-Red). We found that the PBM involved in regulating the repair of injured myocardium is wavelength-limited. LED-Red caused cardiomyocytes (CMs) that had exited the cell cycle to divide and proliferate again, and the cell proliferation ratio increased significantly with the accumulation of intracellular photopower. In addition, LED-Red promoted myocardial revascularization and myocardial regeneration, reduced the area of fibrosis in mice with myocardial infarction (MI), and thus improved cardiac contractile function. In regard to the mechanism, miRNA sequencing analysis showed that low-power LED-Red irradiation could induce differential changes in miRNAs in CMs. Among them, miR-136-5p was identified as a cardiac photo-sensitive miRNA and was obviously inhibited after stimulation, which produced a proliferation-promoting effect on CMs. Subsequent luciferase reporter assays confirmed the involvement of Ino80 as a binding target of miR-136-5p in the regulatory process of CM proliferation. Similarly, LED-Red irradiation elevated intracellular Ino80 expression. After knockdown of Ino80, the proliferation-promoting effect of LED-Red on CMs was inhibited. Collectively, this study demonstrates that LED-Red can promote CM proliferation by inhibiting cardiac photo-sensitive miRNA- miR-136-5p expression through targeting Ino80. The findings provided a new potential strategy for the treatment of ischemic cardiomyopathy (ICD).

摘要

光生物调节(PBM)已成为一种涉及调节多种生物效应的替代疗法。在这项研究中,我们通过使用波长为 630nm 的发光二极管(LED-Red)进行非侵入性照射,验证了 PBM 是否可以影响小鼠的心脏生理活动。我们发现,调节受损心肌修复的 PBM 受到波长限制。LED-Red 导致已退出细胞周期的心肌细胞再次分裂和增殖,并且细胞增殖比例随着细胞内光功率的积累而显著增加。此外,LED-Red 促进了心肌再血管化和心肌再生,减少了心肌梗死(MI)小鼠的纤维化面积,从而改善了心脏收缩功能。关于其机制,miRNA 测序分析表明,低功率 LED-Red 照射可诱导心肌细胞中 miRNAs 的差异变化。其中,miR-136-5p 被鉴定为心脏光敏感 miRNA,刺激后明显受到抑制,对心肌细胞产生促进增殖的作用。随后的荧光素酶报告基因检测证实了 Ino80 作为 miR-136-5p 调节 CM 增殖过程中的结合靶标。同样,LED-Red 照射可提高细胞内 Ino80 的表达。敲低 Ino80 后,LED-Red 对 CM 的促增殖作用受到抑制。综上所述,本研究表明,LED-Red 通过靶向 Ino80 抑制心脏光敏 miRNA—miR-136-5p 的表达,促进 CM 增殖。这些发现为治疗缺血性心肌病(ICD)提供了一种新的潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84eb/9066112/defc709b3be7/ijbsv18p2980g001.jpg

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