机构地区:[1]天津市第五中心医院中心实验室,300450 [2]天津市第五中心医院神经外科,300450 [3]天津市滨海新区中医医院药学科
出 处:《中华老年心脑血管病杂志》2020年第4期410-413,共4页Chinese Journal of Geriatric Heart,Brain and Vessel Diseases
基 金:国家自然科学基金(81471175,81501073);天津市滨海新区卫生计生委科技项目(2015BWKY001)。
摘 要:目的探讨过氧化物酶体增殖物激活受体γ辅激活因子1α(PGC-1α)的小泛素相关修饰蛋白(SUMO)在糖尿病患者血管内皮修复能力下降过程中的作用,并寻找新的治疗方法。方法选取人脐静脉内皮细胞(HUVEC)第3~6代细胞随机分对照组、高糖组及壮观霉素B1治疗组(治疗组)3组(n=4),分别于1.0 g/L葡萄糖、4.5 g/L葡萄糖、4.5 g/L葡萄糖+20μmol/L壮观霉素B1培养液中作用48 h,用Western blot检测SUMO2/3、PGC-1α蛋白表达,RT-PCR方法检测核呼吸因子-2α(NRF-2α)和核受体雌激素受体相关受体α(ERRα)mRNA表达,细胞划痕实验检测HUVEC损伤修复功能,模拟血管形成实验检测HUVEC血管形成能力。结果高糖组和治疗组共价态SUMO2/3蛋白表达水平明显高于对照组,NRF-2α和ERRαmRNA表达水平明显低于对照组(P<0.05,P<0.01);治疗组共价态SUMO2/3蛋白表达水平明显低于高糖组,NRF-2α和ERRαmRNA表达水平明显高于高糖组(P<0.05)。高糖组游离态SUMO2/3水平低于对照组和治疗组(P<0.05)。3组PGC-1α蛋白表达水平比较,无统计学差异(P>0.05)。细胞划痕实验显示,高糖组和治疗组细胞迁移距离明显低于对照组[(19.47±4.04)μm vs(57.35±5.59)μm,P=0.017;(31.98±6.05)μm vs(57.35±5.59)μm,P=0.032],治疗组细胞迁移距离明显高于高糖组(P=0.037)。细胞模拟血管形成实验显示,治疗组能够改善网状交联情况,形成少量类血管结构。结论壮观霉素B1能够通过抑制PGC-1α蛋白的SUMO化修饰增加血管内皮细胞在高糖环境下的自愈能力。Objective To study the role of PPAR-γcoactivator-1α(PGC-1α)-SUMOylation in reducing the repair capacity of endothelial cells in DM patients.Methods The 3-6 passage HUVEC were divided into control group,high glucose group,spectomycin B1 treatment group(4 in each group)and cultured for 48 h in 1.0 g/L glucose,4.5 g/L glucose,4.5 g/L glucose+20μmol/L spectinomycin B1 respectively.The expressions of SUMO 2/3 and PGC-1αprotein were detected by Western blot and those of NRF-2αmRNA and ERRαmRNA were detected by RT-PCR.The repair of HUVEC injury was tested in scratch test and the angiogenesis of HUVEC was assayed in simulated angiogenesis test.Results The expression levels of covalent SUMO2/3 protein were significantly higher while those of NRF-2αmRNA and ERRαmRNA were significantly lower in high glucose group and spectomycin B1 treatment group than in control group(P<0.05,P<0.01).The expression levels of free SUMO 2/3 were significantly lower in high glucose group than in control group and spectomycin B1 treatment group(P<0.05).No significant difference was detected in expression levels of PGC-1αprotein among the 3 groups(P>0.05).Scratch test showed that the migration distance of HUVEC was significantly shorter in high glucose group and spectomycin B1 treatment group than in control group(19.47±4.04μm vs 57.35±5.59μm,P=0.017;31.98±6.05μm vs 57.35±5.59μm,P=0.032)and was significantly longer in spectomycin B1 treatment group than in high glucose group(P=0.037).Simulated angiogenesis test showed that spectomycin B1 treatment could improve the network cross-linking with a small number of vascular structures formed.Conclusion Spectinomycin B1 can improve the self-healing of HUVEC by inhibiting the PGC-1α-SUMOylation in DM patients.
关 键 词:PPARΓ 小泛素相关修饰蛋白质类 糖尿病 核呼吸因子类
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