口腔生物医学 ›› 2022, Vol. 13 ›› Issue (1): 40-44.

• 论著 • 上一篇    下一篇

黄精多糖对乳牙牙髓干细胞增殖及成骨向分化的影响

徐瑞,王锐,高雪峰,郭雨婷,吕学超   

  1. 哈尔滨医科大学附属第一医院
  • 收稿日期:2021-11-22 修回日期:2022-02-19 出版日期:2022-03-25 发布日期:2022-03-21
  • 通讯作者: 吕学超 E-mail:64737994@qq.com
  • 基金资助:
    黑龙江省博士后资助经费

Effects of polygonatum sibiricum polysaccharide on proliferation and osteogenic differentiation of stem cells from human exfoliated deciduous teeth

  • Received:2021-11-22 Revised:2022-02-19 Online:2022-03-25 Published:2022-03-21

摘要: 目的:初步探索不同浓度黄精多糖(PSP)对乳牙牙髓干细胞(SHEDs)增殖及成骨分化能力的影响。方法:分离、培养SHEDs,通过流式细胞术及茜素红染色分别对细胞表面标志物和成骨分化潜能进行鉴定。采用不同浓度PSP处理SHEDs后,CCK-8法检测SHEDs的增殖情况,钙钴法染色和碱性磷酸酶(ALP)试剂盒检测其ALP活性,Western blot法检测其成骨相关蛋白表达情况。结果:流式细胞术及茜素红染色结果显示,所获取的细胞为具有成骨分化能力的SHEDs。与对照组相比,24、48、72 h内各浓度组均对SHEDs增殖无明显影响(P>0.05),25 mg/L PSP组对ALP活性的提升作用最显著,差异具有统计学意义(P<0.001),12.5、25 mg/L PSP组的Runt相关转录因子2(Runx2)及骨钙素(OCN)的蛋白表达均显著上调,其中25 mg/L PSP组对Runx2表达的促进效果最明显,差异具有统计学意义(P<0.001)。结论:PSP对SHEDs的增殖无显著影响,可促进SHEDs成骨分化。

Abstract: Objective: To explore the effects of polygonatum sibiricum polysaccharide (PSP) with different concentrations on the proliferation and osteogenic differentiation of stem cells from human exfoliated deciduous teeth dental pulp (SHEDs). Methods: SHEDs were isolated and cultured. Cells surface markers and osteogenic differentiation potential were identified by flow cytometry and alizarin red staining. After treated with different concentrations of PSP, the proliferation of SHEDs was detected by CCK-8 method, the ALP activity of SHEDs was detected by calcium cobalt staining and alkaline phosphatase (ALP) kit, and the expression of osteogenic proteins was detected by Western blot. Results: The results of flow cytometry and alizarin red staining showed that the obtained cells were SHEDs with osteogenic differentiationability. Compared with the control group, each concentration group had no significant effect on the proliferation of SHEDs within 24, 48 and 72 hours (P>0.05), and the 25 mg/L PSP group had the most significant effect on ALP activity (P<0.001), the protein expressions of runt-related transcription factor 2 (Runx2) and osteocalcin (OCN) in 12.5 and 25 mg/L PSP groups were significantly up-regulated, the 25 mg/L PSP group had the most significant effect on the expression of Runx2 (P<0.001). Conclusions: PSP had no significant effect on the proliferation of SHEDs and can promote the osteogenic differentiation of SHEDs.

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