Total Ginsenoside Extract from Panax ginseng Enhances Neural Stem Cell Proliferation and Neuronal Differentiation by Inactivating GSK-3β

被引:2
|
作者
Lin Kai-li [1 ,2 ,3 ]
Zhang Ji [4 ]
Chung Hau-lam [2 ]
Wu Xin-yi [2 ]
Liu Bin [5 ]
Zhao Bo-xin [6 ]
Sze, Stephen Cho-wing [2 ,3 ]
Zhou Ping-zheng [7 ]
Yung Ken Kin-lam [2 ,3 ]
Zhang Shi-qing [2 ,3 ]
机构
[1] Guangzhou Med Univ, Sch Publ Hlth, Guangzhou 511436, Peoples R China
[2] Hong Kong Baptist Univ HKBU, Dept Biol, Hong Kong 999077, Peoples R China
[3] HKBU Shenzhen Res Inst & Continuing Educ, Shenzhen 518057, Guangdong, Peoples R China
[4] Southern Med Univ, Zhujiang Hosp, Dept Plast Surg, Guangzhou 510515, Peoples R China
[5] Guangzhou Med Univ, Guangzhou Inst Cardiovasc Dis, Affiliated Hosp 2, Guangzhou 510260, Peoples R China
[6] Southern Med Univ, Nanfang Hosp, Dept Pharm, Guangzhou 510515, Peoples R China
[7] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China
基金
中国国家自然科学基金;
关键词
ginsenoside; neural stem cell; proliferation; neuronal differentiation; GSK-3; beta; IN-VIVO; RB1; RD; ALZHEIMERS; PATHWAY; RG1;
D O I
10.1007/s11655-021-3508-1
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective: To study the effects of total ginsenosides (TG) extract from Panax ginseng on neural stem cell (NSC) proliferation and differentiation and their underlying mechanisms. Methods: The migration of NSCs after treatment with various concentrations of TG extract (50, 100, or 200 mu g/mL) were monitored. The proliferation of NSCs was examined by a combination of cell counting kit-8 and neurosphere assays. NSC differentiation mediated by TG extract was evaluated by Western blotting and immunofluorescence staining to monitor the expression of nestin and microtubule associated protein 2 (MAP2). The GSK-3 beta/beta-catenin pathway in TG-treated NSCs was examined by Western blot assay. The NSCs with constitutively active GSK-3 beta mutant were made by adenovirus-mediated gene transfection, then the proliferation and differentiation of NSCs mediated by TG were further verified. Results: TG treatment significantly enhanced NSC migration (P<0.01 or P<0.05) and increased the proliferation of NSCs (P<0.01 or P<0.05). TG mediation also significantly upregulated MAP2 expression but downregulated nestin expression (P<0.01 or P<0.05). TG extract also significantly induced GSK-3 beta phosphorylation at Ser9, leading to GSK-3 beta inactivation and, consequently, the activation of the GSK-3 beta/beta -catenin pathway (P<0.01 or P<0.05). In addition, constitutive activation of GSK-3 beta in NSCs by the transfection of GSK-3 beta S9A mutant was found to significantly suppress TG-mediated NSC proliferation and differentiation (P<0.01 or P<0.05). Conclusion: TG promoted NSC proliferation and neuronal differentiation by inactivating GSK-3 beta.
引用
收藏
页码:229 / 235
页数:7
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