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基于hCMEC/D3人脑微血管内皮细胞探讨血糖波动促进铜稳态失衡致血脑屏障损伤的作用

周勇君 杨洪涛 许永劼 陈迪 李兴 潘卫 朱丽英

实用医学杂志2026,Vol.42Issue(7):1215-1224,10.
实用医学杂志2026,Vol.42Issue(7):1215-1224,10.DOI:10.3969/j.issn.1006-5725.2026.07.014

基于hCMEC/D3人脑微血管内皮细胞探讨血糖波动促进铜稳态失衡致血脑屏障损伤的作用

Exploring the role of blood glucose fluctuations in promoting copper homeostasis imbalance-induced blood-brain barrier injury based on hCMEC/D3 human brain microvascular endothelial cells

周勇君 1杨洪涛 1许永劼 1陈迪 1李兴 2潘卫 1朱丽英1

作者信息

  • 1. 贵州医科大学医学检验学院(贵州贵阳 550004)||贵州医科大学附属医院临床检验中心(贵州贵阳 550004)||贵州医科大学附属医院贵州省产前诊断中心(贵州贵阳 550004)
  • 2. 贵州中医药大学基础医学院(贵州贵阳 550025)
  • 折叠

摘要

Abstract

Objective To investigate the potential effects of glycemic fluctuation on copper homeostasis and blood-brain barrier(BBB)function in hCMEC/D3 human brain microvascular endothelial cells.Methods hCMEC/D3 cells were conventionally cultured and divided into a control group(glucose 25 mmol/L for 4 days)and a fluctuating glucose group(FG group:glucose 25 mmol/L for 8 h followed by glucose 55 mmol/L for 8 h,repeatedly for 4 days).Cell viability was assessed using the CCK-8 assay,and cell morphology was observed under an light microscope.A Transwell system was used to construct a monolayer cell model,and transendothelial electrical resistance(TEER)was measured daily.Monolayer permeability was evaluated using the phenol red assay.Intracellular copper levels and reactive oxygen species(ROS)levels were detected.The mRNA expression levels of copper transporter 1(SLC31A1),copper-transporting ATPase β chain(ATP7B),cytochrome c oxidase copper chaperone 17(COX17),and antioxidant 1 copper chaperone(ATOX1)were determined by qPCR.The protein expression levels of SLC31A1,ATP7B,COX17,ATOX1,zonula occludens-1(ZO-1),occludin,and Claudin-1 were analyzed by Western blot.Results Cell viability in the FG group was significantly lower than that in the control group(P<0.05).Cells in the control group exhibited robust growth and formed a dense network with extensive intercellular connections,whereas cell growth in the FG group was inhibited,with markedly reduced cell numbers and diminished intercellular contacts.The TEER value in the FG group was significantly lower than that in the control group(P<0.05),and the phenol red permeability assay revealed increased permeability and disrupted monolayer integrity in the FG group(P<0.001).Both the copper ion detection kit and copper-specific fluorescent probe showed a significant reduction in intracellular copper levels in the FG group.Intracellular ROS levels were markedly elevated on day 4 in the FG group(P<0.05).qPCR results demonstrated that,compared with the control group,the mRNA expression of ATOX1,COX 17,and SLC31A1 was significantly decreased,whereas ATP7B expression was significantly increased(P<0.05).Western blot analysis showed that the protein expression of ZO-1,occludin,and Claudin-1 was significantly reduced in the FG group(P<0.05).The protein expression of SLC31A1(P<0.05),ATOX1,and COX17 was decreased,while ATP7B expression was increased(P<0.05).Immunofluorescence analysis further confirmed that,compared with the control group,SLC31A1 expression was reduced and ATP7B expression was elevated in the FG group(P<0.05).Conclusion Glycemic fluctuation may impair the structure and function of the BBB in hCMEC/D3 cells by inducing damage to barrier-related structures,increasing cellular permeability,and promoting ROS accumulation.This pathological process may be closely associated with intracellular copper homeostasis imbalance,providing new insights into the mechanisms underlying BBB dysfunction in conditions characterized by glycemic instability.

关键词

糖尿病/血糖波动/血脑屏障/铜稳态失衡/氧化应激/通透性/紧密连接

Key words

diabetes mellitus/glycemic variability/blood-brain barrier/copper homeostasis imbalance/oxidative stress/permeability/tight junctions

分类

医药卫生

引用本文复制引用

周勇君,杨洪涛,许永劼,陈迪,李兴,潘卫,朱丽英..基于hCMEC/D3人脑微血管内皮细胞探讨血糖波动促进铜稳态失衡致血脑屏障损伤的作用[J].实用医学杂志,2026,42(7):1215-1224,10.

基金项目

国家自然科学基金地区科学基金项目(编号:82260165,82560169) (编号:82260165,82560169)

国家自然科学基金青年科学基金项目(编号:82300920) (编号:82300920)

贵州省科技计划项目(编号:黔科合基础-ZK[2024]一般199) (编号:黔科合基础-ZK[2024]一般199)

贵州省卫生健康委科学技术基金项目(编号:gzwkj2024-081) (编号:gzwkj2024-081)

实用医学杂志

1006-5725

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