首页> 外文期刊>Neuroreport >Hyperbaric oxygen promotes neural stem cell proliferation by activating vascular endothelial growth factor/extracellular signal-regulated kinase signaling after traumatic brain injury
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Hyperbaric oxygen promotes neural stem cell proliferation by activating vascular endothelial growth factor/extracellular signal-regulated kinase signaling after traumatic brain injury

机译:高压氧通过在创伤性脑损伤后激活血管内皮生长因子/细胞外信号调节激酶信号来促进神经干细胞增殖

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Hyperbaric oxygen (HBO) therapy and neural stem cell (NSC) transplantation can improve traumatic brain injury (TBI) clinically. This study aimed to investigate the mechanism of HBO promoting NSC proliferation and neurological recovery after TBI. Twenty-four Sprague-Dawley rats were divided randomly into three groups: a sham group, a TBI group (constructed using Feeney's free-fall method), and an HBO-treated TBI group. Neurological function was evaluated by Neurological Severity Scores on days 1, 3, and 7, and we found that TBI-induced poor neurological function was improved by HBO. On day 7 after TBI, we observed that TBI promoted NSC proliferation, migration to the lesion area, and the levels of vascular endothelial growth factor (VEGF), VEGFR2, Raf-1, MEK1/2, and phospho-extracellular signal-regulated kinase (ERK) 1/2 protein, which were further boosted by HBO, from immunohistochemistry, immunofluorescence, and Western blot experiments. In vitro, cell injury was applied to NSCs isolated from neonatal Sprague-Dawley rats by the Cell Injury Controller II system. Moreover, data from the BrdU Kit and Western blot showed that in-vitro HBO significantly accelerated NSC proliferation and the levels of proteins related to cell cycle and the VEGF/ERK pathway after cell injury, which was suppressed by the VEGFR2 inhibitor. Taken together, this study indicated that HBO may promote NSC proliferation by activating VEGF/ERK signaling and play a crucial role in neuroprotection after TBI.
机译:高压氧(HBO)治疗和神经干细胞(NSC)移植可以在临床上改善创伤性脑损伤(TBI)。本研究旨在研究TBI后促进NSC增殖和神经恢复的机制。将二十四只Sprague-Dawley大鼠随机分为三组:假手术组,TBI组(使用Feeney的自由秋季方法构建),以及HBO治疗的TBI组。通过神经系统严重程度评估了神经系统功能在第1,3和7天,并且我们发现HBO改善了TBI诱导的差的神经功能。在第7天在TBI之后,我们观察到TBI促进了NSC的增殖,迁移到病变面积,以及血管内皮生长因子(VEGF),VEGFR2,RAF-1,MEK1 / 2和磷酸盐细胞外信号调节激酶的水平(ERK)1/2蛋白,由HBO进一步升压,免疫组织化学,免疫荧光和蛋白质印迹实验。体外,通过细胞损伤控制器II系统将细胞损伤应用于从新生儿Sprague-Dawley大鼠分离的NSCs。此外,来自Brdu试剂盒和Western印迹的数据表明,体外HBO显着加速了NSC增殖和与细胞周期相关的蛋白质水平和细胞损伤后的VEGF / ERK途径,由VEGFR2抑制剂抑制。这项研究表明,通过激活VEGF / ERK信号传导,HBO可以通过激活VEGF / ERK信号传导,并在TBI后发挥至关重要的作用。

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