葛花提取物通过激活PPARγ上调ABCA1的表达而抑制THP-1源性泡沫细胞形成
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(1.南华大学心血管疾病研究所 动脉硬化学湖南省重点实验室 湖南省动脉硬化性疾病国际科技创新合作基地 南华大学生物信息与医学大数据教研室,湖南省衡阳市 421001;2.湖北文明学院医学部基础医学院,湖北省襄阳市 441053;3.湖南医药学院公共卫生与检验医学院,湖南省怀化市 418000;4.南华大学附属第二医院心血管内科,湖南省衡阳市 421001)

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朱容蓉,硕士研究生,研究方向为动脉粥样硬化病因发病学与防治基础,E-mail:1377615166@qq.com。

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湖南省教育厅科学研究项目(19B490);湖北省自然科学基金青年项目(2023AFB043、2021JJ40485);大学生创新创业项目(S202112214008)


Pueraria Lobata Flowers Extract inhibits THP-1-derived foam cell formation by activating PPARγ to upregulate the expression of ABCA1
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1.Institute of Cardiovascular Disease, University of South China & Key Laboratory for Arteriosclerology of Hunan Province & Hunan International Scientific and Technological Cooperation Base of Arteriosclerotic Disease & Department of Bioinformatics and Medical Big Data, University of South China, Hengyang, Hunan 421001, China;2.Medical Department of Basic Medical College, Hubei University of Arts and Science, Xiangyang, Hubei 441053, China;3.School of Public Health & Laboratory Medicine, Hunan University of Medicine, Huaihua, Hunan 418000, China;4.Department of Cardiology, Second Affiliated Hospital of University of South China, Hengyang, Hunan 421001, China)

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    摘要:

    目的]探寻葛花提取物(PFE)对巨噬细胞源性泡沫细胞脂质蓄积的影响。 [方法]通过MTT法筛选PFE对THP-1源性泡沫细胞的作用浓度,采用油红O染色和胆固醇检测试剂盒检测细胞内脂质蓄积情况,采用胆固醇流出试剂盒检测细胞的胆固醇流出水平,使用RT-qPCR和Western blot检测mRNA和蛋白表达。 [结果]PFE显著降低THP-1源性泡沫细胞内的脂质蓄积。PFE不影响CD36、清道夫受体AⅠ(SR-AⅠ)、固醇调节元件结合蛋白2(SREBP2)及3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)的mRNA表达,但能上调ATP结合盒转运体A1(ABCA1)的mRNA和蛋白表达水平(P<0.05),促进巨噬细胞源性泡沫细胞胆固醇流出(P<0.01)。PFE可以激活过氧化物酶体增殖物激活受体γ(PPARγ)的活性(P<0.01)及上调其mRNA和蛋白表达水平(P<0.05)。与PFE对照组相比,加入GW9662处理后PPARγ和ABCA1的蛋白表达水平均下降(P<0.01),胆固醇流出水平降低(P<0.01)。 [结论]PFE可显著改善THP-1源性泡沫细胞内的脂质蓄积,通过PPARγ上调ABCA1表达及其介导的胆固醇流出抑制泡沫细胞形成。

    Abstract:

    Aim To explore the effect of Pueraria Lobata Flowers Extract (PFE) on lipid accumulation in macrophage-derived foam cells. Methods The concentration of PFE in THP-1-derived foam cells was screened by MTT, intracellular lipid accumulation was detected by oil red O staining and cholesterol detection kit, intracellular cholesterol efflux levels were detected by cholesterol efflux assay kit, RT-qPCR and Western blot were used to analyze mRNA and protein expression. Results PFE significantly reduced lipid accumulation in THP-1-derived foam cells. PFE did not affect the mRNA expression of CD36, scavenger receptor-AⅠ (SR-AⅠ), sterol regulatory element-binding protein 2 (SREBP2), 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCR), but it could upregulate the mRNA and protein expression levels of ATP-binding cassette transporter A1 (ABCA1) (P<0.05), and promote the intracellular cholesterol efflux of macrophage-derived foam cells (P<0.01). PFE could activate the activity of peroxisome proliferator-activated receptor γ (PPARγ) (P<0.01) and upregulate the mRNA and protein expression levels of PPARγ (P<0.05). Compared with the PFE control group, the expression of PPARγ and ABCA1 proteins decreased and cholesterol efflux decreased after GW9662 treatment (all P<0.01). Conclusion PFE could significantly prevent the lipid accumulation in THP-1-derived foam cells and inhibit the formation of foam cells by upregulating ABCA1 expression and cholesterol efflux mediated by PPARγ.

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朱容蓉,陈梦娇,赵真旺,刘嘉怡,吴剑锋,王宇菲,张敏.葛花提取物通过激活PPARγ上调ABCA1的表达而抑制THP-1源性泡沫细胞形成[J].中国动脉硬化杂志,2024,32(5):395~401.

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  • 收稿日期:2023-11-30
  • 最后修改日期:2024-02-08
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  • 在线发布日期: 2024-05-09