口腔生物医学 ›› 2023, Vol. 14 ›› Issue (2): 74-79,96.

• 论著 • 上一篇    下一篇

氢氧化钙糊剂对大鼠骨髓间充质干细胞成骨分化的影响

马艳霞1,李泽汉1,曹灵2,张筱岚1,于金华1*   

  1. 1. 南京医科大学附属口腔医院牙体牙髓科,江苏省口腔疾病研究重点实验室,江苏省口腔转化医学工程研究中心
    2. 南京医科大学附属口腔医院牙体牙髓科
    3. 南京医科大学附属口腔医院儿童口腔预防科,江苏省口腔疾病研究重点实验室,江苏省口腔转化医学工程研究中心
    4. 南京医科大学附属口腔医院儿童牙病科
    5. 南京医科大学附属口腔医学院
  • 收稿日期:2023-02-13 修回日期:2023-02-27 出版日期:2023-06-25 发布日期:2023-07-31
  • 通讯作者: 于金华 E-mail:yuziyi_yjh@hotmail.com
  • 基金资助:
    国家自然科学基金面上项目;国家自然科学基金面上项目

Effect and mechanism of calcium hydroxide paste on rat odontogenic / osteogenic differentiation of BMMSCs

  1. 1. Department of Endodontics, The Affiliated Stomatological Hospital of Nanjing Medical University, Jiangsu Province Key Laboratory of Oral Diseases, Jiangsu Province Engineering Research Center of Stomatological Translational Medicine
    2. Addiliated Hospital of Stomatology, Nanjing Medical University
    3.
    4. Department of Pediatric and Preventive Dentistry, The Affiliated Stomatological Hospital of Nanjing Medical University, Jiangsu Province Key Laboratory of Oral Diseases, Jiangsu Province Engineering Research Center of Stomatological Translational Medicine
  • Received:2023-02-13 Revised:2023-02-27 Online:2023-06-25 Published:2023-07-31

摘要: 目的:研究氢氧化钙糊剂浸提液对大鼠骨髓间充质干细胞(BMMSCs)成骨向分化的影响,为其临床使用提供理论依据。方法:全骨髓贴壁法分离培养大鼠BMMSCs,流式细胞仪进行细胞鉴定,不同条件诱导细胞后进行茜素红染色、油红O染色及阿利新蓝染色,鉴定细胞成骨、成脂及成软骨分化能力。将氢氧化钙糊剂烘干、研磨成粉后,制作氢氧化钙糊剂浸提液及氢氧化钙糊剂条件培养基(CH),使用不同浓度CH(0、0.02、0.2、1、1.5、2 g/L)培养大鼠BMMSCs,碱性磷酸酶(ALP)活性测定筛选最佳作用浓度用于后续实验。大鼠BMMSCs经CH诱导后,ALP染色、ALP活性测定、茜素红染色检测其ALP活性及矿化能力的变化,Western blot检测细胞成骨相关指标Ⅰ型胶原α1(COL1A1)、ALP、Runt相关转录因子2(RUNX2)、成骨相关转录因子(OSX)的表达水平变化。结果:成功分离培养了大鼠BMMSCs,具有成骨、成脂及成软骨分化等间充质干细胞特性;0.2 g/L为CH诱导大鼠BMMSCs ALP活性的最佳作用浓度(P<0.01),使用该浓度CH培养基处理大鼠BMMSCs后,COL1A1、ALP、RUNX2、OSX表达上调(P<0.01)。结论:氢氧化钙糊剂浸提液可促进大鼠BMMSCs成骨分化。

Abstract: Objective: To investigate the effect of calcium hydroxide paste extract on the osteogenic differentiation of rat BMMSCs, and to provide theoretical basis for the clinical use of calcium hydroxide paste. Methods: Rat BMMSCs were isolated and cultured by whole bone marrow adherent method, and identified by flow cytometry. After induced by different conditions, Alizarin red staining, oil red O staining and alcian blue staining were used to identify the osteogenic, adipogenic and chondrogenic differentiation ability of stem cells. Calcium hydroxide paste was dried and ground into powder, then calcium hydroxide paste extract and calcium hydroxide paste conditioned medium (CH) were prepared. After being cultured with different concentrations of CH (0, 0.02, 0.2, 1, 1.5, 2 g/L), ALP activity was measured to screen the best concentration for subsequent experiments. ALP staining, ALP activity assay and alizarin red staining were used to detect the changes in ALP activity and mineralization ability after CH induction. Western blot was used to detect the expression levels of COL1A1, ALP, RUNX2, and OSX. Results: Rat BMMSCs were successfully isolated and the cells had the characteristics of mesenchymal stem cells such as osteogenic, adipogenic and chondrogenic differentiation. 0.2 g/L was the optimal concentration of CH in inducing ALP activity of rat BMMSCs(P<0.01). The expressions of COL1A1, ALP, RUNX2 and OSX were up-regulated after the cells were treated with 0.2 g/L CH(P<0.01). Conclusion: Calcium hydroxide paste extract can potentially promote the osteogenic capacity of rat BMMSCs.