重组人淀粉原蛋白对SHED成骨分化潜能的影响。

IF 5.1 2区 生物学 Q2 CELL BIOLOGY
Cells Pub Date : 2025-04-30 DOI:10.3390/cells14090657
Akira Hirabae, Ryo Kunimatsu, Yuki Yoshimi, Kodai Rikitake, Shintaro Ogashira, Ayaka Nakatani, Shuzo Sakata, Kotaro Tanimoto
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引用次数: 0

摘要

本研究旨在探讨淀粉原蛋白如何改善人类脱落乳牙(SHED)干细胞的骨再生并促进组织愈合,作为治疗临界尺寸骨缺损的一种方法。用成骨分化培养基诱导SHED向骨分化。实时聚合酶链反应、碱性磷酸酶(ALP)染色和定量、茜素红S染色、钙和骨钙素定量评估分化情况。第18天,RUNX2、CBFB、BGLAP、COL1、BMP2、BMP4、NOTCH1、NOTCH2和NES的表达显著增加。骨钙素基因表达继续显著升高。在第7、10和14天,淀粉原素处理组的ALP活性显著高于对照组。第14天,淀粉原素处理组ALP染色增强。第21天,淀粉原素治疗组的钙和骨钙素水平显著高于对照组。本研究提示SHED与淀粉原蛋白联合应用可有效促进骨再生,为再生医学开辟了一条新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Recombinant Human Amelogenin on the Osteogenic Differentiation Potential of SHED.

This study aimed to explore how amelogenin can improve stem cells from human exfoliated deciduous teeth (SHED)-based bone regeneration and promote tissue healing as a treatment for critical-sized bone defects. SHED was induced into bone differentiation by using osteogenic differentiation medium. Real-time polymerase chain reaction, alkaline phosphatase (ALP) staining and quantification, and Alizarin Red S staining, as well as calcium and osteocalcin quantification were performed to assess differentiation. On day 18, a significant increase was observed in the expression of RUNX2, CBFB, BGLAP, COL1, BMP2, BMP4, NOTCH1, NOTCH2, and NES. Osteocalcin gene expression continued to increase significantly. ALP activity was significantly higher in the amelogenin-treated group than in the control group on days 7, 10, and 14. On day 14, enhanced ALP staining was observed in the amelogenin-treated group. Calcium and osteocalcin levels were significantly higher in the amelogenin-treated group than in the control group on day 21. This study suggests that combining SHED and amelogenin may be effective for bone regeneration, offering a potential new approach in regenerative medicine.

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来源期刊
Cells
Cells Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
9.90
自引率
5.00%
发文量
3472
审稿时长
16 days
期刊介绍: Cells (ISSN 2073-4409) is an international, peer-reviewed open access journal which provides an advanced forum for studies related to cell biology, molecular biology and biophysics. It publishes reviews, research articles, communications and technical notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided.
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