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Quercetin Promotes Proliferation and Differentiation of Oligodendrocyte Precursor Cells After Oxygen/Glucose Deprivation-Induced Injury
Authors:Xiuxiang Wu  Xuebin Qu  Qiang Zhang  Fuxing Dong  Hongli Yu  Chen Yan  Dashi Qi  Meng Wang  Xuan Liu  Ruiqin Yao
Affiliation:1. Department of Neurobiology, Xuzhou Medical College, Xuzhou, 221002, Jiangsu, People’s Republic of China
2. Department of Rheumatology and Immunology, Affiliated Hospital of Inner Mongolia Medical University, 1 Tong Dao Bei Jie, Huimin District, Hohhot, 010050, People’s Republic of China
Abstract:The aim of this study was to investigate quercetin’s (Qu) ability to promote proliferation and differentiation of oligodendrocyte precursor cells (OPCs) under oxygen/glucose deprivation (OGD)-induced injury in vitro. The results showed that after OGD, OPCs survival rate was significantly increased by Qu as measured by Cell Counting Kit-8. Furthermore, Qu treatment reduced apoptosis of OPCs surveyed by Hoechst 33258 nuclear staining. Qu at 9 and 27 μM promoted the proliferation of OPCs the most by Brdu and Olig2 immunocytochemical staining after OGD 3 days. Also, Qu treatment for 8 days after OGD, the differentiation of OPCs to oligodendrocyte was detected by immunofluorescence staining showing that O4, Olig2, and myelin basic protein (MBP) positive cells were significantly increased compared to control group. Additionally, the protein levels of Olig2 and MBP of OPCs were quantified using western blot and mRNA levels of Olig2 and Inhibitor of DNA binding 2 (Id2) were measured by RT-PCR. Western blot showed a significant increase in Olig2 and MBP expression levels compared with controls after OGD and Qu treatment with a linear does–response curve from 3 to 81 μM. After treatment with Qu compared to its control group, Olig2 mRNA level was significantly up-regulated, whereas Id2 mRNA level was down-regulated. In conclusion, Qu at 3–27 μM can promote the proliferation and differentiation of OPCs after OGD injury and may regulate the activity of Olig2 and Id2.
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