Ao Xu , Ziqing Li , Yangyang Ding , Xiaoyu Wang , Yufang Yang , Lixia Du , Deheng Wang , Shi Shu , Zhifei Wang
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Flow cytometry was used to explore the impact of EA on post-ischemic brain infiltration of NK cells, as well as the activating receptor NKG2D expression and interferon-γ (IFN-γ) production by these infiltrated NK cells.</div></div><div><h3>Results</h3><div>EA significantly alleviated neurological functional deficits and reduced brain infarction in MCAO mice. Abundant NK cells infiltrated into the ischemic hemisphere, but this infiltration was significantly suppressed by EA. Furthermore, EA attenuated NKG2D levels and reduced production of IFN-γ by NK cells in the ischemic brain. Notably, EA's inhibitory effect on post-ischemic NK cell brain infiltration and activation was comparable to that of STAT3 inhibition. The combination of EA and STAT3 inhibition did not result in further enhancement of the inhibitory effect. Moreover, the protective effects of EA against MCAO injury were abolished when STAT3 was activated.</div></div><div><h3>Conclusion</h3><div>Our findings suggest that EA at Shuigou (GV26) and Baihui (GV20) inhibits the post-ischemic brain infiltration and activation of NK cells through STAT3 inhibition, significantly contributing to its therapeutic effects against brain ischemia.</div></div>","PeriodicalId":9302,"journal":{"name":"Brain Research Bulletin","volume":"219 ","pages":"Article 111128"},"PeriodicalIF":3.5000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electroacupuncture suppresses NK cell infiltration and activation in the ischemic mouse brain through STAT3 inhibition\",\"authors\":\"Ao Xu , Ziqing Li , Yangyang Ding , Xiaoyu Wang , Yufang Yang , Lixia Du , Deheng Wang , Shi Shu , Zhifei Wang\",\"doi\":\"10.1016/j.brainresbull.2024.111128\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><div>Electroacupuncture (EA) at Shuigou (GV26) and Baihui (GV20) has shown therapeutic benefits for stroke patients. Given that natural killer (NK) cell infiltration into the brain significantly contributes to the exacerbation of cerebral ischemic injury, this study investigated the impact of EA at Shuigou (GV26) and Baihui (GV20) on post-ischemic brain infiltration and activation of NK cells.</div></div><div><h3>Methods</h3><div>Neurological deficit score, rotarod test, adhesive removal test, and TTC staining were used to evaluate the beneficial effects of EA in middle cerebral artery occlusion (MCAO) mice. The inhibitory effect of EA on STAT3 activation was assessed using Western blot. Flow cytometry was used to explore the impact of EA on post-ischemic brain infiltration of NK cells, as well as the activating receptor NKG2D expression and interferon-γ (IFN-γ) production by these infiltrated NK cells.</div></div><div><h3>Results</h3><div>EA significantly alleviated neurological functional deficits and reduced brain infarction in MCAO mice. 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引用次数: 0
摘要
目的:电针水沟(GV26)和百会(GV20)对中风患者有治疗作用。鉴于自然杀伤(NK)细胞浸润脑部是加重脑缺血损伤的重要原因,本研究探讨了水沟(GV26)和百会(GV20)电针对脑缺血后NK细胞浸润和激活的影响:方法:采用神经功能缺损评分、转体试验、去粘连试验和TTC染色来评估EA对大脑中动脉闭塞(MCAO)小鼠的益处。用 Western 印迹法评估了 EA 对 STAT3 激活的抑制作用。流式细胞术用于探讨EA对缺血后脑内NK细胞浸润的影响,以及这些浸润的NK细胞表达的激活受体NKG2D和产生的干扰素-γ(IFN-γ):结果:EA能明显缓解MCAO小鼠的神经功能缺损并减少脑梗死。大量 NK 细胞浸润缺血半球,但 EA 能显著抑制这种浸润。此外,EA 还降低了 NKG2D 的水平,并减少了缺血大脑中 NK 细胞产生的 IFN-γ。值得注意的是,EA 对缺血后 NK 细胞脑浸润和激活的抑制作用与 STAT3 抑制作用相当。EA 和 STAT3 抑制的联合使用并没有进一步增强抑制作用。此外,当 STAT3 被激活时,EA 对 MCAO 损伤的保护作用被取消:我们的研究结果表明,水沟(GV26)和百会(GV20)EA通过抑制STAT3来抑制脑缺血后NK细胞的浸润和活化,从而大大提高了其对脑缺血的治疗效果。
Electroacupuncture suppresses NK cell infiltration and activation in the ischemic mouse brain through STAT3 inhibition
Aims
Electroacupuncture (EA) at Shuigou (GV26) and Baihui (GV20) has shown therapeutic benefits for stroke patients. Given that natural killer (NK) cell infiltration into the brain significantly contributes to the exacerbation of cerebral ischemic injury, this study investigated the impact of EA at Shuigou (GV26) and Baihui (GV20) on post-ischemic brain infiltration and activation of NK cells.
Methods
Neurological deficit score, rotarod test, adhesive removal test, and TTC staining were used to evaluate the beneficial effects of EA in middle cerebral artery occlusion (MCAO) mice. The inhibitory effect of EA on STAT3 activation was assessed using Western blot. Flow cytometry was used to explore the impact of EA on post-ischemic brain infiltration of NK cells, as well as the activating receptor NKG2D expression and interferon-γ (IFN-γ) production by these infiltrated NK cells.
Results
EA significantly alleviated neurological functional deficits and reduced brain infarction in MCAO mice. Abundant NK cells infiltrated into the ischemic hemisphere, but this infiltration was significantly suppressed by EA. Furthermore, EA attenuated NKG2D levels and reduced production of IFN-γ by NK cells in the ischemic brain. Notably, EA's inhibitory effect on post-ischemic NK cell brain infiltration and activation was comparable to that of STAT3 inhibition. The combination of EA and STAT3 inhibition did not result in further enhancement of the inhibitory effect. Moreover, the protective effects of EA against MCAO injury were abolished when STAT3 was activated.
Conclusion
Our findings suggest that EA at Shuigou (GV26) and Baihui (GV20) inhibits the post-ischemic brain infiltration and activation of NK cells through STAT3 inhibition, significantly contributing to its therapeutic effects against brain ischemia.
期刊介绍:
The Brain Research Bulletin (BRB) aims to publish novel work that advances our knowledge of molecular and cellular mechanisms that underlie neural network properties associated with behavior, cognition and other brain functions during neurodevelopment and in the adult. Although clinical research is out of the Journal''s scope, the BRB also aims to publish translation research that provides insight into biological mechanisms and processes associated with neurodegeneration mechanisms, neurological diseases and neuropsychiatric disorders. The Journal is especially interested in research using novel methodologies, such as optogenetics, multielectrode array recordings and life imaging in wild-type and genetically-modified animal models, with the goal to advance our understanding of how neurons, glia and networks function in vivo.