塔乌罗斯氧胆酸通过EGFR/p-Akt/CREB1通路在介酶体干细胞中增强骨质分化
Hyojin Kang1, Sunsik Yang2, Jun Lee1
1Department of Oral and Maxillofacial Surgery, College of Dentistry, Wonkwang University, 77 Dunsan-ro, Seo-gu, Daejeon 35233, Republic of Korea.
Cells
|June 10, 2023
概括
塔乌尔苏氧胆酸 (TUDCA) 增强了人体介质干细胞 (hMSCs) 的骨质分化. 这个过程涉及表皮生长因子受体 (EGFR) 信号通路,促进骨再生.
科学领域:
- 干细胞生物学 干细胞生物学
- 再生医学是一种再生医学.
- 生物化学 生物化学
背景情况:
- 介质细胞干细胞 (MSC) 对于再生医学至关重要,特别是在骨修复方面.
- 陶氏氧醇酸 (TUDCA) 越来越多地用于基于细胞的疗法.
- 图德卡对hMSCs骨质性分化的影响的确切机制尚未完全理解.
研究的目的:
- 阐明 TUDCA 诱导人类介质干细胞 (hMSC) 骨质基因分化机制.
- 研究表皮生长因子受体 (EGFR) 信号通路在TUDCA介导的骨质生成中的作用.
主要方法:
- 通过WST-1测定来评估细胞增殖.
- 通过性酸酶活性和阿利沙林红色染色确认了骨质分化.
- 量化基因表达与骨分化和信号通路相关,使用实时PCR.
主要成果:
- 图德卡显著增强了hMSC的扩散和骨质分化,以剂量依赖的方式.
- 骨质基因分化基因的升级,特别是表皮生长因子受体 (EGFR) 和cAMP响应元素结合蛋白1 (CREB1).
- 抑制EGFR信号传递显著减少骨质原体分化和CREB1,环林D1和环林E1.1的表达.
结论:
- TUDCA促进了hMSCs的骨质分化.
- EGFR/p-Akt/CREB1信号通路对于TUDCA诱导的骨质生成至关重要.
- 图德卡是治疗骨疾病的一种有前途的治疗剂.
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