口腔生物医学 ›› 2024, Vol. 15 ›› Issue (1): 6-11.

• 论著 • 上一篇    下一篇

根尖牙乳头干细胞来源凋亡囊泡通过调控巨噬细胞糖酵解相关酶的表达影响其炎症表型

曾涵柔1,李长芳2,王可境2,张婧3,胡丽芳1,王 玮2   

  1. 1. 西北工业大学生命学院
    2. 口颌系统重建与再生全国重点实验室
    3. 第四军医大学口腔医院口腔解剖生理学教研室
  • 收稿日期:2023-11-28 修回日期:2023-12-13 出版日期:2024-02-25 发布日期:2024-03-23
  • 通讯作者: 王 玮 E-mail:weiwang_0510@163.com
  • 基金资助:
    国家自然科学基金面上项目;陕西省重点研发计划项目;陕西省重点研发计划项目

ApoVs derived from SCAP modulate the inflammatory phenotype of macrophages by regulating the expression of glycolysis-associated enzymes

  • Received:2023-11-28 Revised:2023-12-13 Online:2024-02-25 Published:2024-03-23

摘要: 目的:探究根尖牙乳头干细胞(SCAP)来源的凋亡囊泡(apoVs)是否通过影响糖酵解相关酶调控巨噬细胞(BMDMs)炎症表型,进而对炎症反应产生调节作用。方法:体外培养鉴定人源SCAP,经星形孢菌素诱导凋亡后提取apoVs并利用扫描电镜、流式细胞术等对其进行表征鉴定。分别以PBS处理、LPS处理及LPS同apoVs共处理大鼠骨髓来源的BMDMs,分为对照组、LPS组及LPS+apoVs处理组。利用流式细胞术检测促炎表型BMDMs表面标志分子CD80、CD86的表达;利用Western Blot检测BMDMs糖酵解相关酶的表达。结果:根尖牙乳头干细胞来源的apoVs能被BMDMs摄取,降低其促炎表型标志分子CD80、CD86的表达,并中GLUT1、GLUT3(P<0.05)的表达显著下调。结论:SCAP来源apoVs能降低促炎型BMDMs的分布,并对其糖酵解相关酶的表达产生影响。

关键词: 根尖牙乳头干细胞, 巨噬细胞, 凋亡囊泡, 糖酵解

Abstract: Objective:?Investigating whether apoptotic vesicles (apoVs) derived from stem cells from apical papilla (SCAP) modulate macrophage inflammatory phenotype by influencing glycolysis-associated enzymes, thereby regulating the inflammatory response. Methods:?Human-derived SCAP were cultured and characterized in vitro. Staurosporine induction was employed to obtain apoVs from SCAP, followed by the characterization and identification of the apoVs using scanning electron microscopy, flow cytometry, and other methods. Experimental groups included a blank control group, an inflammation group and an apoVs group. Rat bone marrow-derived macrophages (BMDMs) were treated with PBS, LPS and LPS in conjunction with apoVs. Using flow cytometry to assess the expression of surface markers CD80 and CD86 on pro-inflammatory macrophages; employing Western blot to detect the expression of glycolytic enzymes in macrophages. Results:?ApoVs derived from SCAP can be taken up by macrophages, reducing the expression of pro-inflammatory phenotype markers CD80 and CD86. Additionally, they exert an impact on glycolysis-associated enzymes, with a significant downregulation observed in the expression of GLUT1 and GLUT3 (P<0.05). Conclusions:?ApoVs derived from SCAP regulate the expression of glycolysis-associated enzymes in macrophages, reducing the distribution of pro-inflammatory phenotype macrophages, thereby modulating the inflammatory response.

Key words: stem cells from apical papilla, macrophages, apoptotic vesicles, glycolysis