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PI3K/GSK-3在LPA诱导PC12细胞凋亡中的作用
引用本文:王亚亚张杰,张兆辉. PI3K/GSK-3在LPA诱导PC12细胞凋亡中的作用[J]. 卒中与神经疾病, 2020, 27(1): 3-8. DOI: 10.3969/j.issn.1007-0478.2020.01.001
作者姓名:王亚亚张杰  张兆辉
作者单位:430060 武汉大学人民医院神经内科[王亚亚 张杰 张兆辉(通信作者)]
摘    要:目的 探讨PI3K/GSK-3通路在溶血磷脂酸(LPA)诱导PC12细胞凋亡中的作用。方法 培养PC12细胞,CCK8测定不同水平LPA处理下PC12细胞的细胞活力,Tunel法测定不同水平LPA处理下PC12细胞的细胞凋亡,测定PI3K、GSK-3抑制剂预处理对LPA诱导的PC12细胞活力和细胞凋亡的影响; Western Blot测定不同水平LPA处理下PC12细胞裂解液的凋亡蛋白酶Caspase 3水平,测定PI3K、GSK-3抑制剂预处理对LPA介导的PC12细胞裂解液Caspase 3水平变化的影响。结果 LPA剂量依赖导致PC12细胞活力下降,PI3K、GSK3α抑制剂能够减轻LPA介导的PC12细胞活力下降,GSK3β抑制剂能够促进LPA介导的PC12细胞活性损失; LPA以剂量依赖的方式诱导PC12细胞凋亡,PI3K、GSK3α抑制剂可减轻LPA介导的PC12细胞凋亡,GSK3β抑制剂可促进LPA介导的PC12细胞凋亡; LPA以剂量依赖的方式增加PC12细胞Caspase 3表达,PI3K、GSK3α抑制剂可抑制LPA介导的PC12细胞Caspase 3表达增加,GSK3β抑制剂可促进LPA介导的PC12细胞Caspase 3表达增加。结论 LPA/PI3K/GSK-3通路在神经细胞死亡的病理生理过程中起重要作用,干预LPA/PI3K/GSK-3通路将是一种潜在的创伤后治疗措施。

关 键 词:溶血磷脂酸 磷脂酰肌醇激酶3 糖原合成激酶3 细胞凋亡

The role of PI3K/GSK-3 in Lysophosphatidic acid induced apoptosis of PC12 cells
Wang Yaya,Zhang Jie,Zhang Zhaohui.. The role of PI3K/GSK-3 in Lysophosphatidic acid induced apoptosis of PC12 cells[J]. Stroke and Nervous Diseases, 2020, 27(1): 3-8. DOI: 10.3969/j.issn.1007-0478.2020.01.001
Authors:Wang Yaya  Zhang Jie  Zhang Zhaohui.
Affiliation:Department of Neurology, Renmin Hospital of Wuhan University, Wuhan 430060
Abstract:ObjectiveTo investigate the role of PI3K/GSK-3 pathway in LPA-induced apoptosis of PC12 cells.Methods PC12 cells were exposed to different levels of Lysophosphatidic acid(LPA),the cell viability was determined with CCK8. Tunel assay was used to determine the apoptosis of PC12 cells treated with different levels of LPA. The cell viability and apoptosis of PC12 cells were assessed in the present of PI3K and GSK-3 inhibitors. Western Blot was used to determine the levels of Caspase 3 in PC12 cells treated with different levels of LPA, and the change of Caspase 3 levels in PC12 cells was assessed in the present of PI3K and GSK-3 inhibitors.Results LPA dose-dependently induced cell activity loss of PC12 cells. PI3K and GSK3 alpha inhibitors could reduce the loss of cell viability induced by LPA. GSK3 beta inhibitor promoted the activity loss of PC12 cells induced by LPA. LPA induced PC12 cell apoptosis in a dose-dependent manner. PI3K and GSK3 alpha inhibitors reduced LPA-mediated PC12 cell apoptosis. GSK3 beta inhibitor promoted LPA-mediated PC12 cell apoptosis.LPA increased the expression level of Caspase 3 in PC12 cells in a dose-dependent manner,PI3K and GSK3 alpha inhibitors reduced the LPA-mediated increase of Caspase 3 expression level in PC12 cells, and GSK3 beta inhibitors promoted the LPA-mediated increase of Caspase 3 expression level in PC12 cells.Conclusion The LPA/PI3K/ GSK-3 pathway played an important role in the pathophysiological process of nerve cell death. Intervention of the LPA/PI3K/GSK-3 pathway would be a potential post-traumatic therapy.
Keywords:Lysophosphatidic acid(LPA)Phosphatidylinositol kinase3(PI3K)Glycogen synthesis kinase 3(GSK-3)Cell apoptosis
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