首页|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

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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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.
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
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.

agedcentral obesityTWEAKFn14NF-κB pathway

赵艳姣、卓娅·买买提乌斯满、刘金玲、王红梅

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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

老年人 中心性肥胖 TWEAK Fn14 NF-κB通路

国家自然科学基金新疆维吾尔自治区自然科学基金新疆维吾尔自治区人民医院院内项目

821602762021D01C16220200207

2024

中华老年多器官疾病杂志
中国人民解放军总医院老年心血管病研究所

中华老年多器官疾病杂志

CSTPCD
影响因子:0.728
ISSN:1671-5403
年,卷(期):2024.23(2)
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