Inhibition of mir-155-5p alleviates cardiomyocyte pyroptosis induced by hypoxia/reoxygenation via targeting SIRT1-mediated activation of the NLRP3 inflammasome.

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Qiuyu Lu, Qingrong Shen, Jinmei Su, Xin Li, Bingyu Xia, Aicun Tang
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引用次数: 0

Abstract

Objective: The hypoxia/reoxygenation (H/R)-induced pyroptosis of cardiomyocytes plays a crucial role in the pathogenesis of myocardial infarction (MI). miR-155-5p represents a promising target for MI therapy. However, its involvement in H/R-induced pyroptosis remains unclear.

Methods: The H/R exposed rat cardiomyocyte H9c2 was utilized as in vitro model, and the expression levels of miR-155-5p and SIRT1 in cells were modulated through cell transfection experiments. Cell proliferative activity was assessed using the Cell counting kit-8 assay. Supernatant lactate dehydrogenase (LDH) activity was determined through colorimetry. The levels of living and dead cell were observed via Calcin-AM/PI staining. Levels of supernatant interleukin (IL)-1β and IL-18 were measured using ELISA assay. The expression levels of miR-155-5p and silent information regulator 1 (SIRT1) mRNA were detected by qRT-PCR. The protein expression levels of SIRT1, NLRP3, N-terminal gasdermin D (GSDMD-N), and Cleaved caspase-1 were evaluated using Western blot analysis. The targeted regulatory relationship between miR-155-5p and SIRT1 was verified using dual luciferase reporter gene assay.

Results: The proliferation activity of H9c2 cells induced by H/R was attenuated, accompanied by severe injury, increased cell death, and the release of a substantial amount of pro-inflammatory cytokines IL-1β and IL-18. In addition, H/R stimulation resulted in the upregulation of miR-155-5p expression and downregulation of SIRT1 expression in H9c2 cells. Suppression of miR-155-5p or overexpression of SIRT1 exhibited ameliorative effects on H/R-induced cellular injury in H9c2 cells and inhibited NLRP3 inflammasome-mediated pyroptosis. The dual-luciferase assay confirmed the direct targeting of SIRT1 by miR-155-5p in H9c2 cells. Furthermore, partial reversal of the inhibitory effect of miR-155-5p inhibitor on H/R-induced NLRP3 inflammasome-mediated pyroptosis in H9c2 cells was observed upon interference with SIRT1 expression.

Conclusion: Inhibition of miR-155-5p alleviates cardiomyocyte pyroptosis induced by H/R via targeting SIRT1-mediated activation of the NLRP3 inflammasome.

抑制mir-155-5p通过靶向sirt1介导的NLRP3炎性体的激活来减轻缺氧/再氧化诱导的心肌细胞焦亡。
目的:缺氧/再氧化(H/R)诱导心肌细胞焦亡在心肌梗死(MI)的发病机制中起着至关重要的作用。miR-155-5p是心肌梗死治疗的一个有希望的靶点。然而,其在H/ r诱导的焦亡中的作用尚不清楚。方法:以H/R暴露大鼠心肌细胞H9c2为体外模型,通过细胞转染实验调节细胞内miR-155-5p和SIRT1的表达水平。使用细胞计数试剂盒-8测定细胞增殖活性。用比色法测定上清乳酸脱氢酶(LDH)活性。Calcin-AM/PI染色观察活细胞和死细胞水平。ELISA法检测上清白细胞介素(IL)-1β和IL-18水平。采用qRT-PCR检测miR-155-5p和SIRT1 mRNA的表达水平。Western blot检测SIRT1、NLRP3、n端gasdermin D (GSDMD-N)、Cleaved caspase-1蛋白表达水平。通过双荧光素酶报告基因测定验证miR-155-5p与SIRT1之间的靶向调控关系。结果:H/R诱导的H9c2细胞增殖活性减弱,损伤严重,细胞死亡增加,大量促炎细胞因子IL-1β和IL-18释放。此外,H/R刺激导致H9c2细胞中miR-155-5p表达上调,SIRT1表达下调。抑制miR-155-5p或过表达SIRT1对H/ r诱导的H9c2细胞损伤有改善作用,并抑制NLRP3炎症小体介导的焦亡。双荧光素酶测定证实了miR-155-5p在H9c2细胞中直接靶向SIRT1。此外,通过干扰SIRT1表达,观察到miR-155-5p抑制剂对H/ r诱导的NLRP3炎症小体介导的H9c2细胞焦亡的抑制作用部分逆转。结论:抑制miR-155-5p通过靶向sirt1介导的NLRP3炎性体的激活来减轻H/R诱导的心肌细胞焦亡。
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来源期刊
Journal of Cardiothoracic Surgery
Journal of Cardiothoracic Surgery 医学-心血管系统
CiteScore
2.50
自引率
6.20%
发文量
286
审稿时长
4-8 weeks
期刊介绍: Journal of Cardiothoracic Surgery is an open access journal that encompasses all aspects of research in the field of Cardiology, and Cardiothoracic and Vascular Surgery. The journal publishes original scientific research documenting clinical and experimental advances in cardiac, vascular and thoracic surgery, and related fields. Topics of interest include surgical techniques, survival rates, surgical complications and their outcomes; along with basic sciences, pediatric conditions, transplantations and clinical trials. Journal of Cardiothoracic Surgery is of interest to cardiothoracic and vascular surgeons, cardiothoracic anaesthesiologists, cardiologists, chest physicians, and allied health professionals.
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