南方医科大学学报 ›› 2015, Vol. 35 ›› Issue (01): 98-.

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线粒体雌激素受体β通过与Bad相互作用抑制非小细胞肺癌细胞的凋亡

谢强,黄作平,刘颖,刘晓,黄磊   

  • 出版日期:2015-01-20 发布日期:2015-01-20

Mitochondrial estrogen receptor β inhibits non-small cell lung cancer cell apoptosis via
interaction with Bad

  • Online:2015-01-20 Published:2015-01-20

摘要: 目的探究线粒体雌激素受体β(ERβ)抑制凋亡刺激诱导非小细胞肺癌细胞死亡的分子机制。方法免疫荧光及western
blotting分析细胞内源ERβ的线粒体定位;检测顺铂与十字孢碱(staurosporine,STS)处理过表达或沉默线粒体ERβ后细胞凋亡
的变化;免疫共沉淀和western blotting分析线粒体ERβ与促凋亡蛋白Bad的相互作用。结果ERβ存在于A549及201T细胞的
线粒体中;过表达或沉默ERβ可以显著减少或增加顺铂与STS诱导的Bax激活及细胞凋亡;线粒体ERβ与促凋亡蛋白Bad相互
作用可能阻抑Bax的活化及线粒体转位。结论线粒体雌激素受体β可以通过与Bad相互作用抑制顺铂或STS诱导非小细胞肺
癌细胞的凋亡,提示线粒体ERβ可能是治疗非小细胞肺癌的一个新靶点。

Abstract: Objective To explore the molecular mechanisms by which mitochondrial estrogen receptor β (ERβ) suppresses
non-small cell lung cancer cell apoptosis induced by apoptotic stimulations. Methods The mitochondrial localization of ERβ in
non-small cell lung cancer cell lines A549 and 201T was determined using immunofluorescence and Western blotting. The
changes of apoptosis of the cells with mitochondrial ERβ overexpression or knockdown in response to cisplatin and STS
treatments were assessed, and mitochondrial ERβ interaction with the pro-apoptotic protein Bad was detected using
co-immunoprecipitation and Western blotting. Results ERβ was localized in the mitochondria in A549 and 201T cells. ERβ
overexpression significantly reduced while ERβ knockdown increased Bax activation and cell apoptosis induced by cisplatin
and STS. Mitochondrial ERβ interaction with pro-apoptotic protein Bad may suppress Bax activation and its translocation to
the mitochondria. Conclusion Mitochondrial ERβ can suppress apoptosis of non-small cell lung cancer cells induced by
cisplatin or STS through interaction with Bad, suggesting the value of mitochondrial ERβ as a new therapeutic target for
treatment of non-small cell lung cancer.