Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro
|更新时间:2026-01-09
|
Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro
Journal of Army Medical UniversityVol. 37, Issue 8, Pages: 767-771(2015)
作者机构:
作者简介:
基金信息:
DOI:
CLC:R285.5;R322.81;R329.28
Published:2015
稿件说明:
移动端阅览
葛红飞,左世伦,李强,谭亮,吴江怡,蒋周阳,喻安永,兰川,胡荣,冯华.青蒿琥酯通过PI3K-Akt通路促进大鼠室管膜下区神经干细胞增殖的体外研究[J].陆军军医大学学报(原第三军医大学学报),2015,37(08 ):767-771. Ge Hongfei,Zuo Shilun,Li Qiang,Tan Liang,Wu Jiangyi,Jiang Zhouyang,Yu Anyong,Lan Chuan,Hu Rong,Feng Hua.Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(08 ):767-771.
葛红飞, 左世伦, 李强, et al. Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro[J]. Journal of Army Medical University, 2015, 37(8): 767-771.
葛红飞,左世伦,李强,谭亮,吴江怡,蒋周阳,喻安永,兰川,胡荣,冯华.青蒿琥酯通过PI3K-Akt通路促进大鼠室管膜下区神经干细胞增殖的体外研究[J].陆军军医大学学报(原第三军医大学学报),2015,37(08 ):767-771. Ge Hongfei,Zuo Shilun,Li Qiang,Tan Liang,Wu Jiangyi,Jiang Zhouyang,Yu Anyong,Lan Chuan,Hu Rong,Feng Hua.Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2015,37(08 ):767-771.DOI:
葛红飞, 左世伦, 李强, et al. Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro[J]. Journal of Army Medical University, 2015, 37(8): 767-771.DOI:
Artesunate promotes proliferation of rat neural stem cells from subventricular zone via PI3K-Akt pathway in vitro
Objective To investigate the effect of artesunate (ART) on proliferation of neural stem cells (NSCs) from subventricular zone (SVZ) in rats. Methods NSCs were treated with different concentrations of ART (0.4
0.8
1.6
and 3.2 μmol/L) for 24 h
and CCK8 assay was used to evaluate the effect of ART on proliferation of NSCs. The PI3K-Akt pathway inhibitor (LY294002) was added in the 0.8 μmol/L ART group to detect its inhibitory effect on the proliferation of NSCs. The results of CCK8 assay were confirmed via Ki-67 fluorescence staining. Western blot assay was used to assess the expressions of Nestin
Akt and p-Akt after treatment for 24 h in different groups as follows: control group
LY294002 group
0.8 μmol/L ART group
and 0.8 μmol/L ART+LY294002 group. Results (1) CCK8 assay showed that the absorbance values at wavelength of 450 nm were significantly higher in the 0.8 μmol/L ART group than in the control group
and decreased to the level of the control group after addition of LY294002 (P0.05). (2) The Ki-67 positive cell number was higher in the 0.8 μmol/L ART group as compared with other groups
and decreased to the level of the control group after addition of LY294002. (3) Western blot results showed that the expression of Nestin and p-Akt were significantly up-regulated in the 0.8 μmol/L ART group
but after addition of LY294002
the expression was lowered (P0.05). Conclusion ART could promote the proliferation of NSCs from the SVZ
and the PI3K-Akt signaling pathway might play an important role in this process.