Lee Hong Ju, Jung Da Hee, Kim Nam Kwen, Shin Hwa Kyoung, Choi Byung Tae
Department of Korean Medical Science, School of Korean Medicine; Graduate Training Program of Korean Medicine for Healthy Aging, Pusan National University, Yangsan, Republic of Korea.
Department of Korean Ophthalmology, Otolaryngology and Dermatology, School of Korean Medicine, Pusan National University, Yangsan, Republic of Korea.
Neural Regen Res. 2022 Jul;17(7):1556-1565. doi: 10.4103/1673-5374.330611.
Neural/glial antigen 2 (NG2)-expressing cells has multipotent stem cell activity under cerebral ischemia. Our study examined the effects of electroacupuncture (EA) therapy (2 Hz, 1 or 3 mA, 20 minutes) at the Sishencong acupoint on motor function after ischemic insult in the brain by investigating the rehabilitative potential of NG2-derived cells in a mouse model of ischemic stroke. EA stimulation alleviated motor deficits caused by ischemic stroke, and 1 mA EA stimulation was more efficacious than 3 mA EA stimulation or positive control treatment with edaravone, a free radical scavenger. The properties of NG2-expressing cells were altered with 1 mA EA stimulation, enhancing their survival in perilesional brain tissue via reduction of tumor necrosis factor alpha expression. EA stimulation robustly activated signaling pathways related to proliferation and survival of NG2-expressing cells and increased the expression of neurotrophic factors such as brain-derived neurotrophic factor, tumor growth factor beta, and neurotrophin 3. In the perilesional striatum, EA stimulation greatly increased the number of NG2-expressing cells double-positive for oligodendrocyte, endothelial cell, and microglia/macrophage markers (CC1, CD31, and CD68). EA therapy also greatly activated brain-derived neurotrophic factor/tropomyosin receptor kinase B and glycogen synthase kinase 3 beta signaling. Our results indicate that EA therapy may prevent functional loss at the perilesional site by enhancing survival and differentiation of NG2-expressing cells via the activation of brain-derived neurotrophic factor -induced signaling, subsequently ameliorating motor dysfunction. The animal experiments were approved by the Animal Ethics Committee of Pusan National University (approval Nos. PNU2019-2199 and PNU2019-2884) on April 8, 2019 and June 19, 2019.
在脑缺血情况下,表达神经/胶质抗原2(NG2)的细胞具有多能干细胞活性。我们的研究通过在缺血性中风小鼠模型中研究源自NG2的细胞的修复潜力,探讨了电针(EA)疗法(2赫兹,1或3毫安,20分钟)刺激四神聪穴位对脑缺血损伤后运动功能的影响。电针刺激减轻了缺血性中风引起的运动功能障碍,且1毫安电针刺激比3毫安电针刺激或自由基清除剂依达拉奉阳性对照治疗更有效。1毫安电针刺激改变了表达NG2细胞的特性,通过降低肿瘤坏死因子α表达提高了它们在损伤周边脑组织中的存活率。电针刺激有力地激活了与表达NG2细胞增殖和存活相关的信号通路,并增加了神经营养因子如脑源性神经营养因子、肿瘤生长因子β和神经营养素3的表达。在损伤周边纹状体中,电针刺激显著增加了表达NG2细胞中少突胶质细胞、内皮细胞和小胶质细胞/巨噬细胞标志物(CC1、CD31和CD68)双阳性的细胞数量。电针疗法还极大地激活了脑源性神经营养因子/原肌球蛋白受体激酶B和糖原合酶激酶3β信号通路。我们的结果表明,电针疗法可能通过激活脑源性神经营养因子诱导的信号通路增强表达NG2细胞的存活和分化,从而防止损伤周边部位的功能丧失,进而改善运动功能障碍。动物实验于2019年4月8日和2019年6月19日获得釜山国立大学动物伦理委员会批准(批准号分别为PNU2019 - 2199和PNU2019 - 2884)。