口腔医学 ›› 2023, Vol. 43 ›› Issue (6): 494-499.doi: 10.13591/j.cnki.kqyx.2023.06.003

• 基础研究 • 上一篇    下一篇

低氧预处理人羊膜间充质干细胞来源外泌体在改善血管衰老中的作用研究

赵炜1,2,3,刘金明1,2,3,杨磊婷1,2,3,沈铭1,2,3,张静露1,3   

  1. 1 江苏省口腔疾病研究重点实验室,江苏南京(210029)
    2 南京医科大学附属口腔医院综合诊疗科,江苏南京(210029)
    3 江苏省口腔转化医学工程研究中心,江苏南京(210029)
  • 修回日期:2023-03-02 出版日期:2023-06-28 发布日期:2023-07-06
  • 基金资助:
    国家自然科学基金青年基金(81400535);江苏省自然科学基金项目(BK20221302);江苏省科教能力提升工程——江苏省研究型医院(YJXYYJSDW4);江苏省医学创新中心(CXZX202227)

Study on the role of human amniotic mesenchymal stem cell-derived exosomes cultured under hypoxic condition in delaying vascular aging

ZHAO Wei1,2,3,LIU Jinming1,2,3,YANG Leiting1,2,3,SHEN Ming1,2,3,ZHANG Jinglu1,3   

  1. Jiangsu Province Key Laboratory of Oral Diseases,Nanjing 210029, China
  • Revised:2023-03-02 Online:2023-06-28 Published:2023-07-06

摘要:

目的 明确低氧预处理人羊膜间充质干细胞来源的外泌体(human amniotic mesenchymal stem cell-derived exosomes, hAMSC-exos)是否在改善血管衰老中发挥作用。方法 D-半乳糖(D-galactose, D-gal)诱导人脐静脉内皮细胞(human umbilical vein endothelial cells,HUVEC)亚急性衰老,收集低氧预处理hAMSC-exos作用于D-gal诱导衰老的HUVEC,通过衰老相关β-半乳糖苷酶(senescence-associated β-galactosidase, SA-β-Gal)活性染色,P53、P16和γH2AX蛋白表达水平测定HUVEC的衰老水平变化,通过划痕实验、transwell小室迁移实验和成管实验来检测HUVEC的成血管功能变化。结果 D-gal诱导能够成功构建HUVEC亚急性衰老模型;SA-β-Gal检测及P53、P16和γH2AX蛋白表达检测显示低氧预处理hAMSC-exos可更好地逆转D-gal诱导HUVEC导致的SA-β-Gal、P53、P16和γH2AX上调;划痕实验、transwell小室迁移实验和成管实验结果显示,低氧预处理hAMSC-exos可改善D-gal诱导的HUVEC的成血管功能下调。结论 本研究初步明确了低氧预处理hAMSC-exos能改善HUVEC的衰老表型。

关键词: 人羊膜间充质干细胞, 低氧, 外泌体, 人脐静脉内皮细胞, 衰老

Abstract:

Objective To analyze the role of human amniotic mesenchymal stem cell-derived exosomes(hAMSC-exos) cultured under hypoxic condition in delaying vascular aging. Methods D-galactose(D-gal) stimulation was used to induce subacute senescence in human umbilical vein endothelial cells(HUVEC). Hypoxia-induced hAMSC-exos(Hy hAMSC-exos) was collected to incubate with D-gal-induced HUVEC. Senescence of HUVEC was evaluated by senescence-associated β-galactosidase activity (SA-β-Gal) staining. Protein expression levels of P53, P16 and γH2AX, angiogenic function of HUVEC were detected by scratch assay, transwell migration assay and tube formation assay. Results Subacute senescence model of HUVEC was successfully constructed via D-gal stimulation; SA-β-Gal and detection of protein expression levels of P53, P16 and γH2AX showed that Hy hAMSC-exos could reverse the upregulation of β-Gal, P53, P16 and γH2AX caused by D-gal-induced HUVEC; scratch assay, transwell migration assay and tube formation assay showed that Hy hAMSC-exos could alleviate the weakened angiogenic function of HUVEC induced by D-gal. Conclusion The study indicates that Hy hAMSC-exos could alleviate vascular aging.

Key words: human amniotic mesenchymal stem cell (hAMSC), hypoxia, exosomes, human umbilical vein endothelial cells (HUVEC), senescence

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