Wang Xun-Cui, Wang Xiu, Li Qing-Lin
Zhongguo Zhong Yao Za Zhi. 2014 Jan;39(1):106-12.
To study the protective effect of puerarin on MPP(+) -induced SH-SY5Y cells by chaperone-mediated autophagy (CMA).
The Parkinson's disease cell model was established by injuring SH-SY5Y cells with 1 mmol x L(-1) MPP+. The CCK-8 staining was adopted to detect the effect the puerarin of different concentrations on the survival rate of MPP(+)-induced SH-SYSY cells. The autophagosome formation was observed under transmission electron microscope. The AO staining showed the changes in the lysosome activity. RT-PCR was used to detect the changes in Lamp2a and Hsc70 mRNA expressions. The western blotting was adopted to test the expressions of Lamp2a, Hsc70 and alpha-synuclein protein in cells.
Within the concentration range of 12. 5-50.0 micromol x L(-1), the pretreatment with puerain for 30 minutes could protect the injury of MPP+ in SH-SY5Y cells, and showed a certain dose-effect relationship. The AO staining and electron microscope showed the effect of puerain within the concentration range of 12.5-50.0 micromol x L(-1) on 1 mmol x L(-1) MPP(+)-induced SH-SY5Y cells; autophagosomes emerged in cells, and increased along with the rise in the puerarin dose. The results of the flow cytometry revealed that 50.0 micromol x L(-1) of puerarin could protect against the increase of the ROS level in 1 mmol x L(-1) MPP(+) -induced SH-SY5Y cells and prevent the oxidative injury. The results of RT-PCR and western blotting indicated that puerain within the concentration range of 12.5-50.0 micromol x L(-1) alleviated the MPP(+)-induced SH-SY5Y cell injury, and inhibited the accumulation of alpha-synuclein proteins in MPP(+) -induced SH-SY5Y cells by up-regulating Hsc70, Lamp2a mRNA and protein level.
Puerarin could protect against the MPP(+) -induced cell injury, whose protective mechanism may be related to the chaperone-mediated autophagy pathway of interventional molecules.
研究葛根素通过伴侣介导的自噬(CMA)对1-甲基-4-苯基吡啶离子(MPP(+))诱导的SH-SY5Y细胞的保护作用。
用1 mmol/L MPP(+)损伤SH-SY5Y细胞建立帕金森病细胞模型。采用CCK-8染色检测不同浓度葛根素对MPP(+)诱导的SH-SY5Y细胞存活率的影响。在透射电子显微镜下观察自噬体的形成。AO染色显示溶酶体活性的变化。采用RT-PCR检测溶酶体相关膜蛋白2a(Lamp2a)和热休克蛋白70(Hsc70)mRNA表达的变化。采用蛋白质免疫印迹法检测细胞中Lamp2a、Hsc70和α-突触核蛋白的表达。
在12.550.0 μmol/L浓度范围内,葛根素预处理30分钟可保护SH-SY5Y细胞免受MPP(+)损伤,并呈现一定的剂量效应关系。AO染色和电子显微镜观察显示,在12.550.0 μmol/L浓度范围内,葛根素对1 mmol/L MPP(+)诱导的SH-SY5Y细胞有作用;细胞中出现自噬体,并随葛根素剂量增加而增多。流式细胞术结果显示,50.0 μmol/L葛根素可保护1 mmol/L MPP(+)诱导的SH-SY5Y细胞中活性氧水平升高,防止氧化损伤。RT-PCR和蛋白质免疫印迹法结果表明,在12.5~50.0 μmol/L浓度范围内,葛根素可减轻MPP(+)诱导的SH-SY5Y细胞损伤,并通过上调Hsc70、Lamp2a mRNA和蛋白水平抑制MPP(+)诱导的SH-SY5Y细胞中α-突触核蛋白的积累。
葛根素可保护细胞免受MPP(+)诱导的损伤,其保护机制可能与干预分子伴侣介导的自噬途径有关。