肿瘤坏死因子样细胞凋亡弱诱导物/成纤维细胞生长因子诱导早期反应蛋白14轴及下游核因子κB通路的关键因子mRNA及蛋白表达差异与老年肥胖的相关性
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(新疆维吾尔自治区人民医院综合保健内科二病区,乌鲁木齐 830000)

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R589.2

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国家自然科学基金(82160276); 新疆维吾尔自治区自然科学基金(2021D01C162); 新疆维吾尔自治区人民医院院内项目(20200207)


Correlation between obesity and difference of mRNA and protein expression of key factors of tumor necrosis factor-like weak inducer of apoptosis/fibroblast growth factor-induced early reactive protein 14 and downstream nuclear factor-kappa B pathway in the elderly
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(Second Department of Cadre Health Care Center, People′s Hospital of Xinjiang Uygur Autonomous Region, Urumqi 830000, China)

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    摘要:

    目的 研究老年人外周血单个核细胞(PBMC)中肿瘤坏死因子样细胞凋亡弱诱导物(TWEAK)/成纤维细胞生长因子诱导早期反应蛋白14(Fn14)轴及下游核因子κB(NF-κB)通路的关键因子mRNA及蛋白表达差异与老年人中心性肥胖的相关性。方法 2017年9月至2018年5月在新疆农牧区常住居民横断面流行病学调查数据库中随机抽取80例研究对象,根据是否为中心性肥胖分为对照组(n=40)和中心性肥胖组(n=40),提取空腹外周血中PBMC,采用待实时荧光定量聚合酶链反应、Western blotting方法检测TWEAK、Fn14、IκB激酶α(IKKα)、IκB激酶β(IKKβ)、NF-κBp65的mRNA、蛋白表达。采用SPSS 26.0软件进行数据分析。根据数据类型,组间比较分别采用t检验及χ2检验。相关性分析采用双变量Pearson相关分析法。结果 中心性肥胖组外周血PBMC中的Fn14、IKKα、IKKβ的mRNA表达高于对照组(P<0.05);TWEAK、NF-κBp65的mRNA表达也高于对照组,但差异无统计学意义(P>0.05)。中心性肥胖组的Fn14、IKKα、IKKβ蛋白表达水平高于对照组(P<0.05),两组间TWEAK、NF-κBp65蛋白表达水平差异无统计学意义(P>0.05)。双变量Pearson相关性分析显示,上述因子的mRNA表达水平,TWEAK与Fn14呈正相关(r=0.472;P<0.01),Fn14与IKKα、IKKβ均呈正相关(r=0.262,0.275;P<0.05);IKKα、IKKβ与NF-κBp65均呈正相关(r=0.747,0.692;P<0.01)。结论 新疆农牧区常驻老年人中心性肥胖与外周血PBMC中Fn14、IKKα、IKKβ的蛋白、mRNA的高表达相关,TWEAK/Fn14可能通过调节IKK激活NF-κB炎症通路,参与人类肥胖的发生、发展。

    Abstract:

    Objective To study the correlation between central obesity and the difference of mRNA and protein expression of the tumor necrosis factor-like weak inducer of apoptosis (TWEAK)/fibroblast growth factor-induced early reactive protein 14(Fn14)and downstream nuclear factor-kappa B(NF-κB)pathway in peripheral blood mononuclear cells (PBMC) in the elderly. Methods From September 2017 to May 2018,80 subjects were randomly selected from the database of cross-sectional epidemiological survey of permanent residents in agricultural and pastoral areas of Xinjiang. According to whether they had central obesity or not, they were divided into the control group (n=40) and the central obesity group (n=40). PBMC were extracted from fasting peripheral blood, and the mRNA and protein expressions of TWEAK, Fn14, inhibitor of kappa B kinase-α (IKKα), inhibitor of kappa B kinase-β (IKKβ) and NF-κBp65 were detected by quantitative real-time polymerase chain reaction and Western-blotting. SPSS 26.0 was used for statistical analysis. Data comparison between two groups was performed using t-test or χ2 test, depending on data type. Correlation was analyzed using bivariate Pearson correlation analysis method. Results The mRNA expression of Fn14, IKK α, IKK β, TWEAK and NF-κBp65 in PBMC in the central obesity group was higher than that in the control group, but the difference was not statistically significant (P>0.05). The protein expression levels of Fn14, IKK α and IKK β in the central obesity group were higher than those in the control group (P<0.05), but there was no significant difference in TWEAK and NF-κBp65 protein expression between the two groups (P>0.05). Bivariate Pearson correlation analysis showed that mRNA expression of the above factors was positively correlated with TWEAK and Fn14 (r=0.472; P<0.01), Fn14 was positively correlated with IKK α and IKK β(r=0.262,0.275; P<0.05), and that IKK α and IKK β were positively correlated with NF- κBp65 (r=0.747,0.692; P<0.01). Conclusion Central obesity in the elderly in the agricultural and pastoral areas of Xinjiang is related to the high expression of Fn14, IKK α, IKK β and mRNA in peripheral blood PBMC. TWEAK/Fn14 may be involved in the occurrence and development of human obesity by regulating IKK to activate NF- κB inflammatory pathway.

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赵艳姣,卓娅·买买提乌斯满,刘金玲,王红梅.肿瘤坏死因子样细胞凋亡弱诱导物/成纤维细胞生长因子诱导早期反应蛋白14轴及下游核因子κB通路的关键因子mRNA及蛋白表达差异与老年肥胖的相关性[J].中华老年多器官疾病杂志,2024,23(2):81~86

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  • 收稿日期:2023-04-08
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  • 在线发布日期: 2024-02-27
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