首页|CWI1-2通过抑制NLRP3介导的焦亡对缺血性脑卒中模型的保护作用

CWI1-2通过抑制NLRP3介导的焦亡对缺血性脑卒中模型的保护作用

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目的 探索CWI1-2通过抑制NLRP3介导的焦亡对缺血性脑卒中模型起保护作用.方法 通过GEO数据库数据,筛选m6A差异基因.构建缺血性脑卒中动物模型,分为NC组(空白对照组)、缺血性脑卒中组(CIS组)和缺血性脑卒中+[胰岛素样生长因子2 mRNA结合蛋白2(IGF2BP2)抑制剂]CWI1-2组(CIS+CWI1-2组).TTC和HE染色法检测各组造模情况.免疫荧光检测NeuN、TUNEL和NLRP3表达强度.WB检测各组中NLRP3、Caspase-1、IL-1β和GSDMD的表达情况.结果 生物信息学结果提示IGFBP2在CIS患者中高表达.动物模型结果显示,相较于NC组,CIS组中脑梗死面积增多,而较于CIS组,CIS+CWI1-2组的梗死面积减小.HE结果显示,CIS组中细胞核碎裂较多,而较于CIS组,CIS+CWI1-2组的细胞核部分恢复.免疫荧光结果提示,相较于NC组,CIS组中NeuN表达下降,而NLRP3表达上升,TUNEL荧光强度增高;而较于CIS组,CIS+CWI1-2组中NeuN表达上升和NLRP3表达下降,TUNEL荧光强度下降.WB结果显示,相较于NC组,CIS组中NLRP3、Caspase-1、IL-1β和GSDMD上升.相较于CIS组,CIS+CWI1-2组中NLRP3、Caspase-1、IL-1β和GSDMD下降.结论 CWI1-2通过抑制NLRP3介导的焦亡对缺血性脑卒中模型起保护作用.
CWI1-2 protects ischemic stroke model by inhibiting NLRP3-mediated pyroptosis
Objective To investigate the protective effect of CWI1-2 in ischemic stroke models by inhibi-ting NLRP3-mediated pyroptosis.Methods m6A differential genes were screened using data from the GEO database.Animal models of ischemic stroke were established and divided into three groups:the NC group(normal control group),the cerebral ischemic stroke(CIS group)group,and the cerebral ischemic stroke+[insulin-like growth factor 2 mRNA-binding protein 2(IGF2BP2)inhibitor]CWI1-2group(CIS+CWI1-2 group).TTC and HE staining were performed to assess the modeling of each group.Immunofluorescence was utilized to detect the expression intensities of NeuN,TUNEL,and NLRP3.Western blot(WB)analysis was conducted to examine the expression levels of NLRP3,Caspase-1,IL-1β,and GSDMD in each group.Results Bioinformatics results indicated that IGF2BP2 was highly expressed in patients with CIS.Animal model re-sults showed that the infarction area in the CIS group was significantly increased compared to the NC group,whereas the infarction area in the CIS+CWI1-2 group was decreased compared to the CIS group.HE staining revealed increased nuclear fragmentation in the CIS group,with partial nuclear recovery observed in the CIS+CWI1-2 group.Immunofluorescence results indicated that compared to the NC group,the CIS group exhibited decreased NeuN expression,increased NLRP3 expression,and heightened TUNEL fluorescence intensity.However,in the CIS+CWI1-2 group,NeuN expression was increased,NLRP3 expression was decreased,and TUNEL fluorescence intensity was reduced compared to the CIS group.WB results demonstrated elevated pro-tein expression levels of NLRP3,Caspase-1,IL-1β,and GSDMD in the CIS group compared to the NC group,with decreased expression levels of these proteins observed in the CIS+CWI1-2 group compared to the CIS group.Conclusion CWI1-2 exerts a protective effect in the ischemic stroke model by inhibiting NLRP3-me-diated pyroptosis.

insulin-like growth factor 2 mRNA-binding protein 2 inhibitorNLR family,the thermal protein domain contains protein 3stroke

张影影、杨维、李敏、赵宏、寿广丽

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蚌埠医科大学第二附属医院神经内科,安徽 蚌埠 233000

胰岛素样生长因子2mRNA结合蛋白2抑制剂 NLR家族,热蛋白结构域包含蛋白3 卒中

2024

右江民族医学院学报
右江民族医学院

右江民族医学院学报

影响因子:0.708
ISSN:1001-5817
年,卷(期):2024.46(6)