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中国临床药理学与治疗学 ›› 2020, Vol. 25 ›› Issue (3): 271-277.doi: 10.12092/j.issn.1009-2501.2020.03.005

• 基础研究 • 上一篇    下一篇

尖吻蝮蛇毒抑瘤组分I通过增强子结合蛋白同源蛋白/半胱氨酸天冬氨酸蛋白酶-12途径诱导人舌鳞癌Tca8113细胞凋亡的研究

柴 琳1,王振杰2,徐 冉1   

  1. 1皖南医学院口腔医学院,芜湖 241001,安徽;2皖南医学院病理生理学教研室,芜湖 241001,安徽
  • 收稿日期:2019-10-28 修回日期:2020-02-26 出版日期:2020-03-26 发布日期:2020-04-13
  • 作者简介:柴琳,女,副教授,研究方向:肿瘤分子病理学。 Tel:13965190969 E-mail:869319562@qq.com
  • 基金资助:
    安徽省高校自然科学研究重点项目(KJ2017A255);皖南医学院重点科研培育基金(WK2015Z08);芜湖市科技计划项目(2015CXY11);皖南医学院大学生科研资助金项目(WK2019S24)

Apoptosis of Tca8113 cell induced by antitumor component-I from Agkistrodon acutus venom through CHOP/Caspase-12 pathway

CHAI Lin 1, WANG Zhenjie 2, XU Ran 1   

  1. 1 School of Stomatology, Wannan Medical College, Wuhu 241001, Anhui, China; 2 Department of Pathophysiology, Wannan Medical College, Wuhu 241001, Anhui, China
  • Received:2019-10-28 Revised:2020-02-26 Online:2020-03-26 Published:2020-04-13

摘要: 目的:探讨内质网应激途径在尖吻蝮蛇毒抑瘤组分I(antitumor component-I from Agkistrodon acutus venom,AAVC-I)诱导人舌鳞癌Tca8113细胞凋亡中的作用。方法:本实验选择人舌鳞癌Tca8113细胞作为研究对象,体外条件下传代培养取对数生长期细胞进行实验。根据实验目的设为正常对照组、二硫苏糖醇(DL-dithiothreitol,DTT)阳性对照组和AAVC-I实验浓度组。MTT法检测不同浓度的DTT和AAVC-I处理Tca8113细胞24 h后的增殖抑制作用并筛选合适的DTT阳性对照实验浓度和AAVC-I实验浓度组,采用HE染色、Annexin V-FITC/PI双荧光染色法观察细胞凋亡情况,Western blot检测内质网应激葡萄糖调节蛋白78(glucose-regulated protein 78,GRP78)、增强子结合蛋白同源蛋白(enhance-binding protein-homologous protein,CHOP)、半胱氨酸天冬氨酸蛋白酶-12(Caspase-12)、半胱氨酸天冬氨酸蛋白酶-9(Caspase-9)、半胱氨酸天冬氨酸蛋白酶-3(Caspase-3)的表达水平。结果:随着AAVC-I实验浓度的增加,其对Tca8113细胞的增殖抑制作用增强(P<0.05),并观察到细胞皱缩变小间隙增大,胞核浓缩,细胞破碎,出现凋亡小体,凋亡率增高(P<0.05),蛋白GRP78、CHOP、Caspase-12、Caspase-9、Caspase-3表达水平上调(P<0.05)。结论:在AAVC-I诱导人舌鳞癌Tca8113细胞凋亡中,内质网应激CHOP/Caspase-12途径发挥着正向调节作用。

关键词: 内质网应激, 人舌鳞癌Tca8113细胞, 蛇毒

Abstract: AIM: To investigate the effect of endoplasmic reticulum stress pathway on the apoptosis of tongue squamous cancer Tca8113 cells induced by antitumor component-I from Agkistrodon acutus venom (AAVC-I). METHODS: The in vitro experiments were performed on subculture tongue squamous cancer Tca8113 cells in their growth period. A normal control group, a DL-dithiothreitol (DTT) positive control group and different AAVC-I concentrations were set according to the experiment objective. MTT assay was used to detect the proliferation inhibition of Tca8113 cells after been treated with different concentrations of DTT and AAVC-I for 24 h. The results were used to choose appropriate concentrations of DTT and AAVC-I in DTT positive control group and AAVC-I treated group, respectively. HE staining and Annexin V-FITC/PI double fluorescence staining were used to monitor the apoptosis of Tca8113 cells. Western blot was used to identify the expression levels of apoptosis-related proteins including endoplasmic reticulum stress glucose-regulatory protein 78 (GRP78), enhance-binding protein-homologousprotein (CHOP), cysteine-containing aspartate specific protease-12 (Caspase-12), cysteine-containing aspartate specific protease-9 (Caspase-9) and cysteine-containing aspartate specific protease-3 (Caspase-3).RESULTS:The proliferation inhibition of Tca8113 cells increased with an increased concentration of AAVC-I concentration (P<0.05), causing cell shrinkage, increased cell gaps, cytonuclear condensation, cell fragmentation, the appearance of apoptotic bodies, and increased rate of apoptosis (P<0.05). In addition, the expression level of GRP78 protein, CHOP protein, proteins of Caspase-12, Caspase-9 and Caspase-3 were increased (P<0.05).CONCLUSION: Endoplasmic reticulum stress CHOP/Caspase-12 pathway plays an important role in AAVC-I induced Tca8113 cells apoptosis.

Key words: endoplasmic reticulum stress, tongue squamous cancer Tca8113 cells, snake venom

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