《口腔颌面外科杂志》 ›› 2015, Vol. 25 ›› Issue (2): 102-. doi: 10.3969/j.issn.1005-4979.2015.02.004

• 基础研究 • 上一篇    下一篇

釉基质蛋白对大鼠脂肪源性干细胞体外成骨分化能力的实验研究

黄乐,华咏梅   

  1. 同济大学口腔医学院正畸教研室,口腔生物医学转化医学实验室,上海   200072
  • 出版日期:2015-04-22 发布日期:2015-06-10
  • 通讯作者: 华咏梅,主任医师. E-mail:yongmeihua@tongji.edu.cn
  • 作者简介:黄乐(1986—),女,安徽宿州人,住院医师,硕士.

Enamel Matrix Protein Mediates Rats Adipose-Derived Stem Cells Differentiation In Vitro

HUANG Le, HUA Yong-mei   

  1. Department of Orthodontics, Laboratory of Oral Biomedical Science and Translational Medicine, School of  Stomatology, Tongji University, Shanghai 200072, China
  • Online:2015-04-22 Published:2015-06-10

摘要: [摘要] 目的:通过配制不同浓度的釉基质蛋白(enamel matrix proteins,EMPs)培养液,体外培养SD大鼠脂肪源性干细胞(adipose-derived stem cells, ADSCs),初步探究EMPs对ADSCs体外增殖活性及成骨分化能力的影响。方法:酶消化法获得大鼠脂肪间充质细胞,通过流式细胞仪技术分离、筛选干细胞 ,多向诱导分化对所得细胞进行鉴定;乙酸法制备EMPs干粉并通过蛋白免疫印记技术鉴定其成分,配制不同浓度的诱导液以备用;采用MTT法检测EMPs对ADSCs增殖活性的影响,并用实时荧光定量PCR及蛋白免疫印迹的方法检测EMPs诱导ADSCs成骨分化标志物的mRNA及蛋白表达变化情况。结果:釉基质蛋白(EMPs)对大鼠脂肪源性干细胞(ADSCs)的增殖具有明显的促进作用(P<0.05),并呈现剂量和时间依赖性; EMPs培养ADSCs 14 d后,成骨分化标志物Runx-2、Osteocalcin(OCN)、Collagen(Col-I) 在mRNA和蛋白水平表达均增加,并且与EMPs成正比(P<0.05)。结论:釉基质蛋白可作为一种成骨诱导剂,能有效增强大鼠脂肪源性干细胞体外增殖活性并诱导其成骨分化。

关键词: 釉基质蛋白;  , 脂肪源性干细胞;  , 细胞增殖;  , 成骨分化

Abstract: Objective: This study aimed to explore the impact of enamel matrix proteins(EMPs) on proliferation activity and osteogenic differentiation capacity of SD rat adipose-derived stem cells in vitro.  Methods: Adipose-derived stem cells (ADSCs) were isolated from subcutaneous fat pads of healthy male SD rats aged 4 weeks by enzyme digestion method .  Stem cells are separated and identified by flow cytometry technology. EMPs were extracted from tooth germs of heathy male pigs aged 4-6 months. SDS-PAGE electrophoresis technique was used to identify its characteristics, and frozen-dried powder were prepared for subsequent experiments. Effects of EMPs on cell proliferation were assessed by MTT assay. Effects of EMPs on osteogenic differentiation of rat ADSCs were analyzed by Q-PCR and Western-Blot technique.Osteogenic differentiation markers of Osteocalcin(OCN), Runx-2, Collagen I(Col-I) were detected. Results: MTT assay showed that EMPs could enhance rat ADSC proliferation in a dose-dependent and time-dependent manner(P<0.05). Results of Q-PCR and Western-blot technique indicated that EMPs promoted expressions of Runx-2, Col-I and OCN at the mRNA level and protein level without osteo-induction medium(P<0.05). Conclusion: Enamel matrix proteins may be used as an osteoinductive agent, due its enhancing effect on adipose-derived stem cells proliferation and osteogenic differentiation.

Key words: enamel matrix derivative, adipose derived stem cells, proliferation, osteogenic differentiation

中图分类号: