Repetitive Transcranial Magnetic Stimulation Promotes Neural Stem Cell Proliferation and Differentiation after Intracerebral Hemorrhage in Mice*

被引:36
|
作者
Cui, Mengchu [1 ]
Ge, Hongfei [1 ]
Zeng, Han [2 ]
Yan, Hongxiang [1 ]
Zhang, Le [3 ]
Feng, Hua [1 ]
Chen, Yujie [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Dept Neurosurg, 29 Gaotanyan St, Chongqing 400038, Peoples R China
[2] Southwest Univ, Coll Comp & Informat Sci, Chongqing, Peoples R China
[3] Sichuan Univ, Coll Comp Sci, Chengdu, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
repetitive transcranial magnetic stimulation; intracerebral hemorrhage; neural stem cell; proliferation; differentiation; mitogen-activated protein kinase; BRAIN-INJURY; ASTROCYTES; NEURONS; NEUROGENESIS; GENERATION; DEPRESSION; CONVERSION;
D O I
10.1177/0963689719834870
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Repetitive transcranial magnetic stimulation (rTMS) is a physical treatment applied during recovery after intracerebral hemorrhage (ICH). With in vivo and in vitro assays, the present study sought to investigate how rTMS influences neural stem cells (NSCs) after ICH and the possible mechanism. Following a collagenase-induced ICH, adult male C57BL/6 J mice were subjected to rTMS treatment every 24 h for 5 days using the following parameters: frequency, 10 Hz; duration, 2 s; wait time, 5.5 s; 960 trains (500 mu V/div, 5 ms/div, default setting). Brain water content and neurobehavioral score were assessed at days 1, 3, and 5 after ICH. The proliferation and differentiation of NSCs were observed using immunofluorescence staining for Nestin, Ki-67, DCX, and GFAP on day 3 after ICH, and rTMS treatment with the same parameters was applied to NSCs in vitro. We found that rTMS significantly reduced brain edema and alleviated neural functional deficits. The mice that underwent ICH recovered faster after rTMS treatment, with apparent proliferation and neuronal differentiation of NSCs and attenuation of glial differentiation and GFAP aggregation. Accordingly, proliferation and neuronal differentiation of isolated NSCs were promoted, while glial differentiation was reduced. In addition, microarray analysis, western blotting assays, and calcium imaging were applied to initially investigate the potential mechanism. Bioinformatics showed that the positive effect of rTMS on NSCs after ICH was largely related to the MAPK signaling pathway, which might be a potential hub signaling pathway under the complex effect exerted by rTMS. The results of the microarray data analysis also revealed that Ca2+ might be the connection between physical treatment and the MAPK signaling pathway. These predictions were further identified by western blotting analysis and calcium imaging. Taken together, our findings showed that rTMS after ICH exhibited a restorative effect by enhancing the proliferation and neuronal differentiation of NSCs, potentially through the MAPK signaling pathway.
引用
收藏
页码:568 / 584
页数:17
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