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慢病毒介导Notch配体Delta1-RNA干扰对人牙髓干细胞增殖与分化的影响

[Effect of Notch ligand Delta1-RNA interference by lentivirus on proliferation and differentiation of human dental pulp stem cells].

作者信息

Wang Xue-fei, Zhang Gang, Qiu Song-bo, He Fei, Tan Ying-hui, Chen Qian

机构信息

Department of Oral and Maxillofacial Surgery, Xinqiao Hospital, The Third Military Medical University, Chongqing 400037, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2011 Dec;46(12):730-4.

Abstract

OBJECTIVE

To investigate the effects of specific RNA interference (RNAi) to Notch ligand Delta1 on proliferation and differentiation of human dental pulp stem cells (DPSC).

METHODS

DPSC were infected by lentivirus vectors carrying Delta1-RNAi. DPSC were divided into three groups, DPSC/Delta1-RNAi group, DPSC/wt group and DPSC/vector group as control. Cell counting kit-8 (CCK-8) assay and flow cytometry were used to evaluate the proliferation of DPSC. Expression of proliferating cell nuclear antigen (PCNA) was examined with immunohistochemical staining. All groups were cultured in an odonto-inductive medium and were observed under microscope. The number of mineralization nodules was counted after Alizarin red staining. Alkaline phosphatase (ALP) activity and the expression of dentin sialophosphoprotein (DSPP) were detected by ALP activity assay and Western blotting.

RESULTS

Compared with DPSC/wt or DPSC/vector separately, proliferating rate and S-cycle of DPSC/Delta1-RNAi was significantly lower. The S phase and proliferation index (PI) decreased markedly from 22.32 ± 2.35 and 33.68 ± 4.19 (DPSC/Delta1-RNAi) to 5.44 ± 0.91 and 16.00 ± 6.07 (DPSC/wt). The PCNA staining of DPSC/Delta1-RNAi was evidently weaker. DPSC/Delta1-RNAi group had more calcified cell nodules than the other two control groups, and ALP activity and DSPP expression of DPSC/Delta1-RNAi group increased markedly.

CONCLUSIONS

Delta1-RNAi induced by the lentivirus vectors may inhibit DPSC proliferation and differentiation. Notch-Delta signal pathway plays an important role in self-renewal and differentiation.

摘要

目的

研究特异性RNA干扰(RNAi)Notch配体Delta1对人牙髓干细胞(DPSC)增殖和分化的影响。

方法

用携带Delta1-RNAi的慢病毒载体感染DPSC。将DPSC分为三组,即DPSC/Delta1-RNAi组、DPSC/wt组和作为对照的DPSC/载体组。采用细胞计数试剂盒-8(CCK-8)法和流式细胞术评估DPSC的增殖情况。用免疫组织化学染色检测增殖细胞核抗原(PCNA)的表达。所有组均在成牙本质诱导培养基中培养,并在显微镜下观察。茜素红染色后计数矿化结节的数量。通过碱性磷酸酶(ALP)活性测定和蛋白质印迹法检测ALP活性和牙本质涎磷蛋白(DSPP)的表达。

结果

与DPSC/wt组或DPSC/载体组相比,DPSC/Delta1-RNAi组的增殖率和S期显著降低。S期和增殖指数(PI)从22.32±2.35和33.68±4.19(DPSC/Delta1-RNAi组)显著降至5.44±0.91和16.00±6.07(DPSC/wt组)。DPSC/Delta1-RNAi组的PCNA染色明显较弱。DPSC/Delta1-RNAi组的钙化细胞结节比其他两个对照组更多,且DPSC/Delta1-RNAi组的ALP活性和DSPP表达明显增加。

结论

慢病毒载体诱导的Delta1-RNAi可能抑制DPSC的增殖和分化。Notch-Delta信号通路在自我更新和分化中起重要作用。

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