Remote limb ischemic postconditioning inhibits microglia pyroptosis by modulating HGF after acute ischemia stroke

• Published in: Bioengineering & translational medicine Vol. 8; no. 6; pp. e10590 - n/a
• Main Authors: Yu, Lu, Zhang, Zuohui, Chen, Hao, Wang, Miao, Mao, Wenqi, Hu, Jinxia, Zuo, Dandan, Lv, Bingchen, Wu, Weifeng, Qi, Suhua, Cui, Guiyun
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.11.2023; Wiley
• Subjects: acute ischemic stroke; Blood pressure; Brain damage; Cell death; Correlation analysis; Cytokines; Damage prevention; Growth factors; Head injuries; high throughput screening; Ischemia; microglial; Occlusion; Pathogenesis; Pore formation; Protein expression; Proteins; pyroptosis; Quantitative analysis; remote limb ischemic postconditioning; Stroke; Student's t-test; Traumatic brain injury; pyroptosis; microglial; acute ischemic stroke; high throughput screening; remote limb ischemic postconditioning
• ISSN: 2380-6761; 2380-6761
• DOI: 10.1002/btm2.10590

The repetitive inflation-deflation of a blood pressure cuff on a limb is known as remote limb ischemic postconditioning (RIPostC). It prevents brain damage induced by acute ischemia stroke (AIS). Pyroptosis, executed by the pore-forming protein gasdermin D (GSDMD), is a type of regulated cell death triggered by proinflammatory signals. It contributes to the pathogenesis of ischemic brain injury. However, the effects of RIPostC on pyroptosis following AIS remain largely unknown. In our study, linear correlation analysis confirmed that serum GSDMD levels in AIS patients upon admission were positively correlated with NIHSS scores. RIPostC treatment significantly reduced GSDMD level compared with patients without RIPostC at 3 days post-treatment. Besides, middle cerebral artery occlusion (MCAO) surgery was performed on C57BL/6 male mice and RIPostC was induced immediately after MCAO. We found that RIPostC suppressed the activation of NLRP3 inflammasome to reduce the maturation of GSDMD, leading to decreased pyroptosis in microglia after AIS. Hepatocyte growth factor (HGF) was identified using the high throughput screening. Importantly, HGF siRNA, exogenous HGF, and ISG15 siRNA were used to reveal that HGF/ISG15 is a possible mechanism of RIPostC regulation in vivo and in vitro.