基础医学与临床 ›› 2021, Vol. 41 ›› Issue (5): 704-708.

• 研究论文 • 上一篇    下一篇

原花青素抑制Aβ25-35诱导的人神经母细胞瘤细胞系SH-SY5Y分泌Aβ1-42

李琪1,2, 张小强1,2*, 陶一凡1,2, 朱孟雯1,2, 崔丹丹1,2, 孙腾腾1,2   

  1. 东南大学 1.公共卫生学院; 2.环境医学工程教育部重点实验室, 江苏 南京 210009
  • 收稿日期:2020-12-09 修回日期:2021-03-20 出版日期:2021-05-05 发布日期:2021-05-06
  • 通讯作者: *zhangxq7843@126.com
  • 基金资助:
    中央高校基本科研业务费专项资金资助和江苏省普通高校研究生科研创新计划资助项目(SJZZ16_0034)

Proanthocyanidins inhibit the secretion of Aβ1-42 induced by Aβ25-35 in human neuroblastoma cell line SH-SY5Y

LI Qi1,2, ZHANG Xiao-qiang1,2*, TAO Yi-fan1,2, ZHU Meng-wen1,2, CUI Dan-dan1,2, SUN Teng-teng1,2   

  1. 1. School of Public Health; 2. Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Southeast University,Nanjing 210009,China
  • Received:2020-12-09 Revised:2021-03-20 Online:2021-05-05 Published:2021-05-06
  • Contact: *zhangxq7843@126.com

摘要: 目的 研究原花青素(PC)对β-淀粉样肽(Aβ25-35)诱导的人神经母细胞瘤细胞系(SH-SY5Y)淀粉样肽产生的影响及可能的作用机制。方法 以Aβ25-35体外处理SH-SY5Y细胞诱导细胞损伤模型,应用PC和(或)Wnt/β-catenin信号通路的内源性抑制剂分泌型蛋白Dickkopf-1(Dkk1)干预。设立对照组、Aβ25-35组、不同浓度PC+Aβ25-35组、Dkk1组和Dkk1+PC+Aβ25-35组。MTT法检测细胞活力;Western blot检测β-catenin、GSK-3β和p-GSK-3β蛋白表达水平;ELISA检测Aβ1-42分泌水平。结果 与对照组相比,Aβ25-35可使细胞活力降低(P<0.05),可降低细胞中β-catenin蛋白和p-GSK-3β蛋白表达水平(P<0.05),增加细胞中Aβ1-42分泌(P<0.05)。PC干预可改善Aβ25-35导致的细胞活力降低(P<0.05),增加细胞中β-catenin蛋白和p-GSK-3β蛋白表达水平(P<0.05),减少Aβ1-42分泌(P<0.05)。应用Dkk1后,PC提高细胞中β-catenin蛋白和p-GSK-3β蛋白表达水平及降低Aβ1-42分泌水平的能力下降(P<0.05)。结论 PC可抑制Aβ25-35诱导的SH-SY5Y细胞Aβ1-42生成,该作用可能与Wnt/β-catenin信号通路有关。

关键词: 原花青素, 1-42, Wnt/β-catenin

Abstract: Objective To investigate the effect of proanthocyanidins(PC) induced by amyloid-beta peptide(Aβ25-35) in human neuroblastoma cell line SH-SY5Y and its possible mechanism. Methods SH-SY5Y cells were exposed to Aβ25-35 to establish a cell injury model in vitro. PC and(or) secretory protein Dickkopf-1 (Dkk1), the endogenic inhibitor of Wnt/β-catenin signaling pathway were used for intervention. The cells were divided into control group, Aβ25-35 group, PC(different concentrations)+Aβ25-35 groups, Dkk1 group, Dkk1+ PC+Aβ25-35 group.The cell viability was evaluated by MTT assay. The expressions of β-catenin, GSK-3β, p-GSK-3β were measured by Western blot. The secreted Aβ1-42 was detected by ELISA. Results Compared with the control group, the cell viability, the expression of β-catenin and p-GSK-3β were reduced in Aβ25-35 treated group(P<0.05), while the secreted Aβ1-42 was increased (P<0.05). PC improved the cell viability, increased the expression of β-catenin and p-GSK-3β, and reduced the secreted Aβ1-42 in SH-SY5Y cells induced by Aβ25-35 (P<0.05). After using Dkk1,the ability of PC was decreased on the enhancement of β-catenin expression, the improvement of p-GSK-3β expression, and the reduction of the secreted Aβ1-42 (P<0.05). Conclusions PC may decrease Aβ1-42 secretion in SH-SY5Y cells induced by Aβ25-35 through Wnt/β-catenin signaling pathway.

Key words: proanthocyanidins, 1-42, Wnt/β-catenin

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