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[Notch激活延缓人牙髓细胞衰老]

[Notch activation delayed ageing of human dental pulp cells].

作者信息

Chang Si-jia, Zou Xiao-ying, Zhuang Heng, Yue Lin, Gao Xue-jun

机构信息

Department of Cariology and Endodontology, Peking University School and Hospital of Stomatology, Beijing 100081, China.

出版信息

Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Feb 18;46(1):5-11.

Abstract

OBJECTIVE

To establish model of dental pulp cells with activated Notch signaling pathway, and investigate the effect of activating Notch signaling pathway on senescence of human dental pulp cells in vitro.

METHODS

Human dental pulp cells were isolated, cultured as usual, and used from the 4(th) passage. The cells were divided into the activated group and the negative control group. In the activated group, the way of coating dishes with Jagged1 protein (10 mg/L) was used to activate Notch signaling pathway. The negative control group cells received no treatment. In the 4(th), 8(th), and 10(th) passages, the expression levels of the Notch signaling pathway downstream gene Hes1 were verified by real-time quantitative PCR (RT-qPCR). The cell changes after activating Notch signaling pathway were observed at three levels: (1) The cell morphology changes were observed through invert phase contrast microscope. The cell activity was detected with MTT assay. (2) The alkaline phosphatase (ALP) expression and its activity, and senescence-associated &bgr;-galatosidase (SA-β-Gal) expression were observed with the kit. (3) The expression changes of senescence related genes were verified using RT-qPCR. The difference between the negative control group and the activated group was analyzed using student's t test.

RESULTS

The expression level of the downstream gene Hes1 of Notch signaling pathway increased after coating the dishes with Jagged1 protein, indicating the establishment of the model of dental pulp cells with activated Notch signaling pathway. Compared with the negative control group, the aging cells of the activated group appeared relatively late. In the 8(th) and 10(th) passage, the cell activity increased. In the 10th passage, ALP activity increased, but SA-β-Gal expression decreased. p16 gene expression decreased in each passage, and p53 gene expression decreased in the 8(th) and 10(th) passages.

CONCLUSION

Jagged1 could activate Notch signaling pathway effectively. Through activating Notch signaling pathway, the dental pulp cells showed a trend of senescence delay at different levels, such as cell morphology, metabolic enzyme expressions and related gene expressions.

摘要

目的

建立Notch信号通路激活的牙髓细胞模型,体外研究激活Notch信号通路对人牙髓细胞衰老的影响。

方法

分离人牙髓细胞,常规培养,取第4代细胞使用。细胞分为激活组和阴性对照组。激活组采用Jagged1蛋白(10 mg/L)包被培养皿的方式激活Notch信号通路。阴性对照组细胞不做处理。在第4、8、10代时,采用实时定量PCR(RT-qPCR)验证Notch信号通路下游基因Hes1的表达水平。从三个层面观察激活Notch信号通路后的细胞变化:(1)通过倒置相差显微镜观察细胞形态变化。采用MTT法检测细胞活性。(2)用试剂盒观察碱性磷酸酶(ALP)表达及其活性,以及衰老相关β-半乳糖苷酶(SA-β-Gal)表达。(3)采用RT-qPCR验证衰老相关基因的表达变化。采用学生t检验分析阴性对照组和激活组之间的差异。

结果

用Jagged1蛋白包被培养皿后,Notch信号通路下游基因Hes1的表达水平升高,表明成功建立了Notch信号通路激活的牙髓细胞模型。与阴性对照组相比,激活组衰老细胞出现相对较晚。在第8、10代时,细胞活性增加。在第10代时,ALP活性增加,但SA-β-Gal表达降低。各代p16基因表达均降低,第8、10代p53基因表达降低。

结论

Jagged1可有效激活Notch信号通路。通过激活Notch信号通路,牙髓细胞在细胞形态、代谢酶表达及相关基因表达等不同层面呈现衰老延迟趋势。

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