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miRNA-7658-5p通过调控氧化应激反应促进同型半胱氨酸诱导的巨噬细胞凋亡

李雪儿 杨慧霞 马润秋 李桂忠 郝银菊 马胜超 姜怡邓 张鸣号

中国病理生理杂志2026,Vol.42Issue(1):52-59,8.
中国病理生理杂志2026,Vol.42Issue(1):52-59,8.DOI:10.3969/j.issn.1000-4718.2026.01.007

miRNA-7658-5p通过调控氧化应激反应促进同型半胱氨酸诱导的巨噬细胞凋亡

miRNA-7658-5p promotes homocysteine-induced macrophage apoptosis by regulating oxidative stress response

李雪儿 1杨慧霞 2马润秋 1李桂忠 2郝银菊 1马胜超 3姜怡邓 1张鸣号2

作者信息

  • 1. 宁夏医科大学,宁夏 银川 750004
  • 2. 宁夏医科大学基础医学院,宁夏 银川 750004
  • 3. 国家卫生健康委代谢性心血管疾病研究重点实验室,宁夏 银川 750004
  • 折叠

摘要

Abstract

AIM:To investigate the function and regulatory mechanism of microRNA-7658-5p(miRNA-7658-5p)in homocysteine(Hcy)-induced apoptosis of mouse macrophages(RAW264.7 cells),as well as its effects on oxida-tive stress and mitochondrial membrane potential.METHODS:Mouse RAW264.7 macrophages were cultured in vitro,and divided into a control group(Hcy:0 µmol/L)and an Hcy-treated group(Hcy:100 µmol/L).Flow cytometry was used to detect the intracellular level of reactive oxygen species(ROS).JC-1 fluorescent staining was employed to observe changes in mitochondrial structure and membrane potential.Western blot was performed to detect the expression levels of apoptosis-related proteins B-cell lymphoma 2(Bcl-2).Bcl-2-associated X protein(Bax);and qRT-PCR was used to de-termine the transcriptional level of miRNA-7658-5p.Furthermore,the cells were transfected with miRNA-7658-5p mim-ic,inhibitor,and negative control,and the above indicators were re-analyzed.Finally,Western blot and flow cytometry were used to detect the expression of apoptosis-related proteins and the cell apoptosis rate.RESULTS:Compared with the control group,the Hcy-treated group showed significantly increased expression of miRNA-7658-5p,expression of Bax protein,and intracellular ROS accumulation(P<0.01),while the expression of Bcl-2 protein and mitochondrial mem-brane potential were significantly decreased(P<0.01).Functional verification experiments showed that overexpression of miRNA-7658-5p enhanced Hcy-induced macrophage apoptosis(P<0.01),whereas inhibition of its expression significant-ly alleviated apoptosis(P<0.01).CONCLUSION:miRNA-7658-5p promotes Hcy-induced macrophage apoptosis by regulating oxidative stress.

关键词

微小RNA-7658-5p/同型半胱氨酸/氧化应激/细胞凋亡

Key words

microRNA-7658-5p/homocysteine/oxidative stress/apoptosis

分类

医药卫生

引用本文复制引用

李雪儿,杨慧霞,马润秋,李桂忠,郝银菊,马胜超,姜怡邓,张鸣号..miRNA-7658-5p通过调控氧化应激反应促进同型半胱氨酸诱导的巨噬细胞凋亡[J].中国病理生理杂志,2026,42(1):52-59,8.

基金项目

癌症、心脑血管、呼吸和代谢性疾病防治研究国家科技重大专项(No.2024ZD0531200) (No.2024ZD0531200)

宁夏回族自治区重点研发计划重点项目(No.2023BEG02074) (No.2023BEG02074)

宁夏回族自治区重点研发计划重点项目(No.2022BFH02013) (No.2022BFH02013)

宁夏医科大学校级重点项目(No.XJKF240311) (No.XJKF240311)

中国病理生理杂志

1000-4718

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