孕期尼古丁暴露所致子代成骨细胞BMP-4/Smad信号通路的变化
投稿时间:2017-07-21  修订日期:2018-01-19  点此下载全文
引用本文:王军建,刘鑫,刘方娜,姚满叶,邓宇.孕期尼古丁暴露所致子代成骨细胞BMP-4/Smad信号通路的变化[J].医学研究杂志,2018,47(11):57-61
DOI: 10.11969/j.issn.1673-548X.2018.11.013
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作者单位E-mail
王军建 450018 郑州儿童医院骨科  
刘鑫 450018 郑州儿童医院骨科  
刘方娜 450018 郑州儿童医院骨科  
姚满叶 450018 郑州儿童医院骨科 wangjunjian19844@sina.com 
邓宇 430071 武汉大学中南医院骨科  
基金项目:国家自然科学基金青年科学基金资助项目(81502817)
中文摘要:目的 探究大鼠孕期尼古丁暴露对子代成骨细胞(OB)BMP-4/Smad信号通路的影响。方法 将妊娠期大鼠分为对照组与实验组,对照组受孕第9天皮下注射2mg/(kg·d)生理盐水,实验组在受孕后第9天于皮下注射2mg/(kg·d)尼古丁,新生3天乳鼠处死后收集颅骨,采用钙钴法对OB碱性磷酸酶进行染色,反转录聚合酶链反应法(RT-PCR)测定OB细胞中骨形态发生蛋白4 (BMP-4)、Smad1、Smad5、Smad8、Runt相关转录因子2(Runx-2)、成骨相关转录因子(Osterix)、Smads泛素化调节因子1(Smurf1)表达,免疫印迹法(Western blot)检测OB中BMP-4、Smad1、Smad5、Smad8、Runx-2、Osterix、Smurf1蛋白表达。结果 ALP染色显示OB细胞胞体较大,细胞核染色呈蓝紫色,细胞质呈淡紫色,对照组ALP细胞阳性率为42.69%±5.16%,高于实验组(18.67%±3.19%),差异有统计学意义(P<0.05)。RT-PCR结果显示实验组BMP-4、Smad1、Smad5、Smad8、Runx-2、Osterix mRNA表达量均低于对照组,Smurf1mRNA表达量高于对照组,差异有统计学意意义(P<0.05)。Western blot法检测结果显示,实验组乳鼠OB中BMP-4、Smad1、Smad5、Smad8、Runx-2、Osterix 蛋白表达量均低于对照组,Smurf1蛋白表达量高于对照组。蛋白条带灰度扫描结果显示,实验组乳鼠OB中BMP-4、Smad1、Smad5、Smad8、Runx-2、Osterix 蛋白相对灰度值均低于实验组,Smurf1蛋白相对灰度值高于对照组,差异有统计学意义(P<0.05)。结论 大鼠孕期尼古丁暴露对OB具有一定的抑制作用,可能与上调Smurf1表达、抑制BMP-4/Smad信号通路和下调转录因子Runx-2、Osterix有关。
中文关键词:尼古丁暴露  子代乳鼠  成骨细胞  BMP-4/Smad信号通路
 
Changes of Osteoblast BMP-4/Smad Signaling Pathway Caused by Nicotine Exposure in Pregnancy
Abstract:Objective To explore the influence of nicotine exposure in pregnancy on osteoblast (OB) BMP-4/Smad signaling pathway. Methods Pregnant rats were divided into control group and experimental group, and the control group were injected with 2mg/ (kg·d) salines ubcutaneously at 9th day in pregnancy, and the experimental group were injected with 2mg/ (kg·d) nicotine. The skull was collected after offspring suckling mice killed at 3rd day. OB alkaline phosphatase was stained by using calcium cobalt method, and bone morphogenetic protein 4 (BMP-4), Smad1, Smad5, Smad8, Runt related transcription factor 2 (Runx-2),osteogenic associated transcription factor (Osterix) and Smads ubiquitination regulator 1 (Smurf1) expression in OB cells were detected by using reverse transcription polymerase chain reaction method (RT-PCR). BMP-4, Smad1, Smad5, Smad8, Runx-2, Osterix,Smurf1 protein expression in OB cells were tested by using Western blot. Results ALP staining showed that OB cells bodies were larger, the nuclei stained blue and purple, and cytoplasm was pale purple. The positive rate of ALP cells in the control group 42.69%±5.16%, higher than that of (19.67%±3.19%) in the experimental group, with statistically significant difference (P<0.05). The results of RT-PCR showed that BMP-4, Smad1, Smad5, Smad8, Runx-2, Osterix and mRNA expression levels in the experimental group were lower than those in the control group. The expression of Smurf1mRNA was higher than that of the control group,with statistically significant difference (P<0.05). The results of Western blot showed that BMP-4, Smad1, Smad5, Smad8, Runx-2 and Osterix expression in OB of the observation group were lower than those in the control group.The expression of Smurf1 protein was higher than that in the control group. The results expression levels of protein stripe gray scale scanning showed that the relative gray values of BMP-4, Smad1, Smad5, Smad8, Runx-2, OB and Osterix in the observation group were lower than those in the observation group,the relative gray value of Smurf1 protein was higher than that of the control group,with statistically significant difference (P<0.05). Conclusion Nicotine exposure in pregnancy has a definite inhibitory effect on OB in rats, and it may be associated with BMP-4/Smad signaling pathways inhibition and down-regulation of transcription factors Runx-2, up regulation of Smurf1.
keywords:Nicotine exposure  Offspring suckling mice  Osteoblast  BMP-4/Smad signaling pathways
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