Yanqin Ying, Jing Tang, Wei Chen, Nan Li
Department of Pediatrics, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China, 430030, China.
Department of Pediatrics, Jinzhou Maternal and Children Healthy Care Hospital, Jinzhou, China, 434020.
Transl Neurosci. 2017 Oct 15;8:102-110. doi: 10.1515/tnsci-2017-0016. eCollection 2017.
The present study evaluates the effect of grifolin (GFL) in oxygen/glucose deprivation (OGD) induced white matter lesion. Injury induced with OGD was found to be significant at the 9th h of OGD induction and the effect of GFL on the proliferation of oligodendrocyte precursor cells (OPCs) was assessed by CCK-8 and Hoechst 33258 assay at GFL 1, 5, 25, 50 and 100 μm concentrations. Whereas immunocytochemistry was performed for the assessment of survival and apoptosis of OPCs, western blot assay and RT-PCR were performed after 8th day of OGD injury for the estimation of expressions of myelin basic protein (MBP) and inhibitor of DNA binding 2 (Id2) in OPCs respectively. Results of the study suggests that treatment with GFL significantly enhances the survival rate and decreases the apoptosis of OPCs in OGD induced injury model. Immunocytochemical staining of Oligodendrocyte transcription factor (Olig2) and Bromodeoxyuridine (Brdu) shows that GFL treatment improves the proliferation of OPCs than OGD group. Moreover data of western blot assay suggested that treatment with GFL significantly enhances the expressions of MBP and Olig2 than OGD. It was observed that expressions of Id2 decreases and Olig2 enhances in GFL treated group than OGD group. Data of our study concludes that GFL enhances the differentiation and proliferation of OPCs in OGD-induced injury by altering the expressions of Id2 and Olig2.
本研究评估了鹰爪豆素(GFL)对氧/葡萄糖剥夺(OGD)诱导的白质损伤的影响。发现OGD诱导的损伤在OGD诱导的第9小时显著,通过CCK-8和Hoechst 33258检测在1、5、25、50和100μm浓度的GFL下评估GFL对少突胶质前体细胞(OPCs)增殖的影响。通过免疫细胞化学评估OPCs的存活和凋亡,在OGD损伤第8天后进行蛋白质免疫印迹分析和逆转录聚合酶链反应(RT-PCR),分别估计OPCs中髓鞘碱性蛋白(MBP)和DNA结合抑制因子2(Id2)的表达。研究结果表明,在OGD诱导的损伤模型中,GFL治疗显著提高了OPCs的存活率并降低了其凋亡率。少突胶质细胞转录因子(Olig2)和溴脱氧尿苷(Brdu)的免疫细胞化学染色显示,与OGD组相比,GFL治疗改善了OPCs的增殖。此外,蛋白质免疫印迹分析数据表明,与OGD相比,GFL治疗显著提高了MBP和Olig2的表达。观察到,与OGD组相比,GFL治疗组中Id2的表达降低而Olig2的表达增强。我们的研究数据得出结论,GFL通过改变Id2和Olig2的表达来增强OGD诱导损伤中OPCs的分化和增殖。