重组人釉原蛋白及猪釉基质蛋白对人骨髓基质细胞成骨作用的比较

上海口腔医学 ›› 2015, Vol. 24 ›› Issue (4): 390-394.

重组人釉原蛋白及猪釉基质蛋白对人骨髓基质细胞成骨作用的比较

林智恺^{1, 2}, 束蓉^{1, 2}, 宋忠臣^{1, 2}, 程岚^{1, 2}, 董家辰^{1, 2}, 张秀丽²

1.上海交通大学医学院附属第九人民医院·口腔医学院牙周病科,上海 200011; 2.上海市口腔医学研究所,上海市口腔医学重点实验室,上海 200011

收稿日期:2014-08-12 出版日期:2015-08-20 发布日期:2015-09-10
通讯作者: 束蓉,Tel: 021-23271699-5510, E-mail:shurong123@hotmail.com E-mail:shurong123@hotmail.com
作者简介:林智恺（1987-）,男,硕士,住院医师,E-mail: zhklin@sina.cn
基金资助:
国家自然科学基金（81070838,81271156）; 上海交通大学医工交叉研究基金（YG2011MS31）

The effect of rhAm and EMPs on promoting differentiation of hBMSCs into osteoblasts

LIN Zhi-kai^{1, 2}, SHU Rong^{1, 2}, SONG Zhong-chen^{1, 2}, CHENG Lan^{1, 2}, DONG Jia-chen^{1, 2}, ZHANG Xiu-li²

1.Department of Periodontology,Shanghai Ninth People’s Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine. Shanghai 200011; 2.Shanghai Research Institute of Stomatology, Shanghai Key Lab of Stomatology. Shanghai 200011, China

Received:2014-08-12 Online:2015-08-20 Published:2015-09-10
Supported by:
Supported by National Natural Science Foundation of China(81070838,81271156) and Biomedical Engineering Cross Research Foundation of Shanghai Jiao Tong University(YG2011MS31)

摘要/Abstract

摘要： 目的比较全长重组人釉原蛋白（recombinant human amelogenin, rhAm）和猪釉基质蛋白（enamel matrix proteins,EMPs）体外诱导人骨髓基质细胞（human bone marrow stromal cells,hBMSCs）成骨分化的作用,探讨rhAm促进hBMSCs成骨的调控机制,为rhAm临床应用提供理论依据。方法经诱导表达并纯化得到25 kDa全长rhAm;利用乙酸法提纯猪EMPs,体外原代培养hBMSCs。采用实时定量PCR及Western印迹法检测不同时间点rhAm和EMPs作用hBMSCs后成骨因子（Runx2、ALP、COL-I）的变化,观察时效关系。采用碱性磷酸酶和茜素红染色检测2种蛋白对hBMSCs成骨矿化作用的影响。采用SPSS 13.0软件包对数据进行统计学分析。结果体外培养获得原代hBMSCs。实时定量PCR、Western印迹及细胞染色结果表明,10 μg/mL rhAm和200 μg/mL EMPs均可明显促进hBMSCs中成骨相关因子的基因及蛋白表达,且这种效果和蛋白作用时间有一定相关性。结论rhAm与EMPs均能明显促进hBMSCs成骨,作用效果具有一定的时间依赖性。

关键词: 牙周组织再生, 釉原蛋白, 釉基质蛋白, 骨髓基质细胞

Abstract: PURPOSE: To compare the effect of recombinant full-length human amelogenin (rhAm) and enamel matrix proteins （EMPs） on differentiation of human bone marrow stromal cells (hBMSCs) into osteoblasts. Meanwhile, to investigate the possible mechanism of rhAm promoting osteogenic differentiation of hBMSCs. METHODS: ThehBMSCs were cultured in vitro. The cells were treated with 10 μg/mL rhAm and 200 μg/mL EMPs. The gene and protein expression of Runx2, ALP, Col-I were observed by using RT-PCR and Western blot at different time points. The influence of rhAm and EMPs on mineralization and osteogenesis of hBMSCs were observed by using alkaline phosphatase and alizarin red staining methods. The data was analyzed with SPSS 13.0 software package. RESULTS: Both rhAm and EMPs significantly promoted gene and protein expression of Runx2, ALP and Col-I in hBMSCs. Meanwhile, rhAm and EMPs also facilitated osteogenesis and mineralization of hBMSCs. The effects of two proteins on hBMSCs had no significant difference. CONCLUSIONS: Both 10 μg/mL rhAm and 200 μg/mL EMPs can significantly promote differentiation of hBMSCs into osteoblasts. The rhAm may be used in inducing periodontal tissue regeneration in the future.

Key words: Periodontal regeneration, Amelogenin, Enamel matrix proteins, Bone marrow stromal cellsn Shanghai J Stomatol, 2015, 24(4):390-394.

中图分类号:

R781.5

林智恺, 束蓉, 宋忠臣, 程岚, 董家辰, 张秀丽. 重组人釉原蛋白及猪釉基质蛋白对人骨髓基质细胞成骨作用的比较[J]. 上海口腔医学, 2015, 24(4): 390-394.

LIN Zhi-kai, SHU Rong, SONG Zhong-chen, CHENG Lan, DONG Jia-chen, ZHANG Xiu-li. The effect of rhAm and EMPs on promoting differentiation of hBMSCs into osteoblasts[J]. Shanghai Journal of Stomatology, 2015, 24(4): 390-394.

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