畜牧兽医学报 ›› 2018, Vol. 49 ›› Issue (12): 2753-2761.doi: 10.11843/j.issn.0366-6964.2018.12.025

• 临床兽医 • 上一篇    下一篇

6-溴-靛玉红-3'-肟抑制脂多糖诱导的小鼠乳腺上皮细胞凋亡

刘畅1, 唐鑫1, 张文劲1, 赵春阳1, 郭爱珍1,2, 胡长敏1,2*   

  1. 1. 华中农业大学 动物医学院, 武汉 430070;
    2. 华中农业大学 农业微生物学国家重点实验室, 武汉 430070
  • 收稿日期:2018-03-26 出版日期:2018-12-23 发布日期:2018-12-23
  • 通讯作者: 胡长敏(1977-),男,土家族,湖北宜昌人,副教授,主要从事动物麻醉及牛疾病的生物学防治研究,E-mail:hcm@mail.hzau.edu.cn
  • 作者简介:刘畅(1992-),女,河南开封人,硕士生,主要从事奶牛乳腺炎研究,E-mail:18771066393@163.com
  • 基金资助:

    国家重点研发计划(2016YFD0500906);国家肉牛/牦牛产业技术体系(CARS-37);中央高校基本科研业务费专项资金(2662015PY054);湖北省自然科学基金(2015CFB435)

6-Bromo-Indirubin-3'-Oxime Inhibits Apoptosis of Mouse Mammary Epithelial Cell Induced by Lipopolysaccharide

LIU Chang1, TANG Xin1, ZHANG Wen-jing1, ZHAO Chun-yang1, GUO Ai-zhen1,2, HU Chang-min1,2*   

  1. 1. College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China;
    2. The State Key Laboratory of Agricultural Microbiology, Huazhong Agricultural University, Wuhan 430070, China
  • Received:2018-03-26 Online:2018-12-23 Published:2018-12-23

摘要:

研究6-溴-靛玉红-3'-肟(BIO)对脂多糖(lipopolysaccharide,LPS)诱导小鼠乳腺上皮细胞(mouse mammary epithelial cell,MMEC)凋亡的作用及机制。收集空白对照组、DMSO组、BIO单独处理组及不同浓度BIO(5、25、50 nmol·L-1)+LPS共同处理组细胞,分别用流式细胞术检测凋亡率,利用qRT-PCR检测BakBaxBcl-2、Bcl-xlCaspase-3和Caspase-8 mRNA的变化,Western blot检测Bcl-2、Caspase-3和Caspase-8蛋白水平的变化。结果显示:BIO能够降低LPS诱导的MMECs的凋亡率,抑制凋亡基因BakBax及凋亡通路蛋白Caspase-3和Caspase-8活性(P<0.001),促进抑凋亡基因Bcl-2及Bcl-xl的活性。BIO通过调节Bax、Bak、Bcl-2、Bcl-xl、Caspase-3和Caspase-8活性抑制LPS诱导的鼠乳腺上皮细胞凋亡。

Abstract:

The aim of this study was to investigate the effects of 6-bromo-indirubin-3'-oxime(BIO) on apoptosis of mouse mammary epithelial cell induced by lipopolysaccharide (LPS) and its regulatory mechanism. The cells from the blank control group, DMSO group, BIO alone treatment group and different concentrations of BIO (5, 25, 50 nmol·L-1 treatment) + LPS co-treatment group were collected, respectively. Apoptosis rate was analyzed by flow cytometry. Bak, Bax, Bcl-2, Bcl-xl, Caspase-3 and Caspase-8 mRNA expression were detected by qRT-PCR. Bcl-2, Caspase-3 and Caspase-8 protein expression were tested by Western blot. Results were as follows:BIO reduced the apoptosis rate of MMECs induced by LPS. BIO decreased LPS-induced activities of apoptosis genes Bak and Bax, apoptotic pathway proteins Caspase-3 and Caspase-8 (P<0.001) were also down-regulated. BIO increased the activities of anti-apoptosis genes Bcl-2 and Bcl-xl. BIO inhibited apoptosis of MMECs induced by LPS through regulating Bax, Bak, Bcl-2, Bcl-xl, Caspase-3 and Caspase-8 activity.

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