DAPT对成牙骨质细胞增殖活性的影响

doi:10.13701/j.cnki.kqyxyj.2016.02.003

口腔医学研究 ›› 2016, Vol. 32 ›› Issue (2): 117-121.DOI: 10.13701/j.cnki.kqyxyj.2016.02.003

DAPT对成牙骨质细胞增殖活性的影响

胡芝爱潘洁李煜昱周泽渊黄鹂邹淑娟^*

四川大学华西口腔医院正畸科四川成都 610041

收稿日期:2015-08-10 出版日期:2016-02-28 发布日期:2016-03-10
通讯作者: 邹淑娟,电话:(028)85501474
作者简介:胡芝爱(1988~),女,湖南人,博士研究生,医师,主要从事口腔正畸的临床治疗工作。
基金资助:
国家自然科学基金(编号:81271178)四川省科技厅支撑项目(编号:2013SZ0043)

Impact of DAPT on the Proliferative Activity of Cementoblast.

HU Zhi-ai, PAN Jie, LI Yu-yu, ZHOU Ze-yuan, HUANG Li, ZOU Shu-juan.

Department of Orthodontics, West China Hospital of Stomatology, Chengdu 610041, China

Received:2015-08-10 Online:2016-02-28 Published:2016-03-10

摘要/Abstract

摘要： 目的:探讨γ-分泌酶抑制剂DAPT对成牙骨质细胞株OCCM30的Notch信号通路是否有抑制作用,及对成牙骨质细胞增殖活性的影响,并初步探讨其作用机制。方法:γ-分泌酶抑制剂DAPT作用于OCCM30细胞,分别培养2、4、6 d,采用RT-PCR检测Notch信号通路下游基因(Hes-1、Hey-1)和细胞周期相关基因(Cyclin D、Cyclin E)的表达,采用流式细胞术检测DAPT对OCCM30细胞周期的影响;DAPT作用于OCCM30细胞后,连续培养8 d,采用CCK-8法测定细胞增殖活性。结果:实验组Hes-1、Hey-1、Cyclin D、Cyclin E mRNA的表达下降,G1/G0期细胞百分比增高,与对照组相比差异有统计学意义(P<0.05);第2~8天,实验组细胞增殖活性(A₄₅₀值)显著降低,呈浓度依赖性,且与对照组相比差异有统计学意义(P<0.05)。结论:DAPT能有效抑制成牙骨质细胞株OCCM30的Notch信号通路,抑制OCCM30细胞的增殖活性,其机制可能与DAPT下调细胞周期相关基因(Cyclin D、Cyclin E)表达有关。

关键词: DAPT, 成牙骨质细胞, OCCM30, Notch信号, 增殖

Abstract: Objective: To clarify whether DAPT (a γ-secretase inhibitor) could inhibit the Notch signaling pathway in the cementoblast OCCM30. To investigate the impact of DAPT on the proliferation of the cementoblast and the mechanism behind. Methods: The OCCM30 cells were cultured with γ-secretase inhibitor DAPT. On day 2, 4 and 6, RT-PCR was conducted to detect the expression of the Notch signaling pathway genes (Hes-1 and Hey-1) and cell cycle related genes (Cyclin D and Cyclin E) and flow cytometry was used to investigate the impact of DAPT on the cell cycle of OCCM30. On day 8, the CCK-8 was carried out for the detection of the proliferative activity of the OCCM30. Results: Compared to the control group, the expression level of Hes-1, Hey-1, Cyclin D and Cycin E in the experimental groups decreased (P<0.05) while the G1/G0 cell proportion increased (P<0.05). From day 2 to day 8, the proliferative activity of the cells in the experimental groups decreased significantly (P<0.05). The proliferative activity of the OCCM30 in the higher DAPT concentration group was lower than that in the lower DAPT concentration group, both of which were significantly lower than the control group (P<0.05).Conclusion: DAPT effectively inhibited the proliferative activity of the OCCM30. The mechanism behind that could be the inhibitory effect of the DAPT on the Notch signaling pathway, down-regulating the expression of the cell-cycle related genes.

中图分类号:

R780.1

胡芝爱,潘洁,李煜昱,周泽渊,黄鹂,邹淑娟. DAPT对成牙骨质细胞增殖活性的影响[J]. 口腔医学研究, 2016, 32(2): 117-121.

HU Zhi-ai, PAN Jie, LI Yu-yu, ZHOU Ze-yuan, HUANG Li, ZOU Shu-juan.. Impact of DAPT on the Proliferative Activity of Cementoblast.[J]. Journal of Oral Science Research, 2016, 32(2): 117-121.

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DAPT对成牙骨质细胞增殖活性的影响

Impact of DAPT on the Proliferative Activity of Cementoblast.

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