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釉基质衍生物刺激ATDC5细胞的软骨形成分化。

Enamel matrix derivative stimulates chondrogenic differentiation of ATDC5 cells.

作者信息

Narukawa M, Suzuki N, Takayama T, Shoji T, Otsuka K, Ito K

机构信息

Department of Periodontology, Dental Research Center, Nihon University School of Dentistry, Tokyo, Japan.

出版信息

J Periodontal Res. 2007 Apr;42(2):131-7. doi: 10.1111/j.1600-0765.2006.00926.x.

Abstract

BACKGROUND AND OBJECTIVES

Although enamel matrix derivative can promote chondrogenic differentiation of pluripotent mesenchymal precursor cells, the molecular mechanism that underlies this phenomenon is unclear. The purpose of this study was to determine the effect of enamel matrix derivative on chondrogenic differentiation. ATDC5 cells, which undergo a reproducible multistep chondrogenic differentiation, were cultured with or without enamel matrix derivative for up to 35 d.

METHODS AND RESULTS

Cell proliferation and alkaline phosphatase activity increased markedly in cells cultured in the presence of enamel matrix derivative, compared with cells cultured in its absence. Deposition of Alcian blue-positive cartilage matrix and Alizarin red-positive mineralized nodules also increased significantly upon treatment with enamel matrix derivative. Expression of mRNAs encoding cartilage extracellular matrix proteins (type II collagen, type X collagen and aggrecan) and chondrogenic-related transcription factors (Sox9, Zfp60 and AJ18) were measured using the real-time polymerase chain reaction. Type II collagen, type X collagen and aggrecan mRNA expression increased markedly with enamel matrix derivative treatment. Transcription of Sox9, an important transcription factor that mediates chondrogenic differentiation, also increased with enamel matrix derivative treatment. The KRAB/C2H2 zinc-finger transcription factors, Zfp60 and AJ18, were transiently expressed in the prehypertrophic stage, and their expression increased with enamel matrix derivative treatment. In a western blot analysis with anti-insulin-like growth factor-I and anti-bone morphogenetic protein-6 immunoglobulin, bands corresponding to approximately 14, approximately 18 and approximately 60 kDa were found in enamel matrix derivative.

CONCLUSION

Our study provides clear evidence that enamel matrix derivative promotes chondrogenic differentiation of ATDC5 cells.

摘要

背景与目的

尽管釉基质衍生物可促进多能间充质前体细胞的软骨形成分化,但其潜在分子机制尚不清楚。本研究旨在确定釉基质衍生物对软骨形成分化的影响。将经历可重复多步骤软骨形成分化的ATDC5细胞,在有或无釉基质衍生物的情况下培养长达35天。

方法与结果

与未添加釉基质衍生物培养的细胞相比,添加该衍生物培养的细胞增殖和碱性磷酸酶活性显著增加。用釉基质衍生物处理后,阿尔新蓝阳性软骨基质和茜素红阳性矿化结节的沉积也显著增加。使用实时聚合酶链反应测量编码软骨细胞外基质蛋白(II型胶原、X型胶原和聚集蛋白聚糖)和成软骨相关转录因子(Sox9、Zfp60和AJ18)的mRNA表达。经釉基质衍生物处理后,II型胶原、X型胶原和聚集蛋白聚糖的mRNA表达显著增加。介导软骨形成分化的重要转录因子Sox9的转录也随釉基质衍生物处理而增加。KRAB/C2H2锌指转录因子Zfp60和AJ18在肥大前期短暂表达,其表达随釉基质衍生物处理而增加。在使用抗胰岛素样生长因子-I和抗骨形态发生蛋白-6免疫球蛋白的蛋白质印迹分析中,在釉基质衍生物中发现了对应于约14 kDa、约18 kDa和约60 kDa的条带。

结论

我们的研究提供了明确证据,表明釉基质衍生物可促进ATDC5细胞的软骨形成分化。

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