小胶质细胞
血管生成
缺血
医学
体内
冲程(发动机)
脑缺血
缺血性中风
血管内皮生长因子
药理学
免疫学
内科学
炎症
生物
血管内皮生长因子受体
生物技术
工程类
机械工程
作者
Masato Kanazawa,Minami Miura,Masafumi Toriyabe,Misaki Koyama,Masahiro Hatakeyama,Masanori Ishikawa,Takashi Nakajima,Osamu Onodera,Tetsuya Takahashi,Masatoyo Nishizawa,Takayoshi Shimohata
摘要
Cell-therapies that invoke pleiotropic mechanisms may facilitate functional recovery in stroke patients. We hypothesized that a cell therapy using microglia preconditioned by optimal oxygen-glucose deprivation (OGD) is a therapeutic strategy for ischemic stroke because optimal ischemia induces anti-inflammatory M2 microglia. We first delineated changes in angiogenesis and axonal outgrowth in the ischemic cortex using rats. We found that slight angiogenesis without axonal outgrowth were activated at the border area within the ischemic core from 7 to 14 days after ischemia. Next, we demonstrated that administration of primary microglia preconditioned by 18 hours of OGD at 7 days prompted functional recovery at 28 days after focal cerebral ischemia compared to control therapies by marked secretion of remodelling factors such as vascular endothelial growth factor, matrix metalloproteinase-9, and transforming growth factor-β polarized to M2 microglia in vitro/vivo. In conclusion, intravascular administration of M2 microglia preconditioned by optimal OGD may be a novel therapeutic strategy against ischemic stroke.
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