Zeste基因抑制子基因12在糖尿病肾脏病模型大鼠肾组织中的表达  

Expression of suppressor of Zeste 12 in kidney tissues of rats with diabetic nephropathy

作　　者：赵璐[1] 赵逸菲 高达[1] 刘艳芳[3] 付婷婷[1] 徐江雁[4] Zhao Lu;Zhao Yifei;Gao Da;Liu Yanfang;Fu Tingting;Xu Jiangyan(Department of Endocrinology,the Third Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450008,Henan Province,China;Longzi Hu Campus,Henan University of Chinese Medicine,Zhengzhou 450046,Henan Province,China;Department of Nephrology,the Third Affiliated Hospital of Henan University of Chinese Medicine,Zhengzhou 450008,Henan Province,China;Henan University of Chinese Medicine,Zhengzhou 450046,Henan Province,China)

机构地区：[1]河南中医药大学第三附属医院内分泌科,河南省郑州市450008 [2]河南中医药大学龙子湖校区,河南省郑州市450046 [3]河南中医药大学第三附属医院肾病科,河南省郑州市450008 [4]河南中医药大学,河南省郑州市450046

出　　处：《中国组织工程研究》2023年第8期1179-1186,共8页Chinese Journal of Tissue Engineering Research

基　　金：国家重点研发计划项目(2020YFE0201800),项目负责人:徐江雁。

摘　　要：背景:Zeste基因抑制子基因12(Suppressor of zeste gene 12,Suz12)可参与肾小管上皮细胞的上皮间质转化。目的:探讨Suz12对糖尿病肾脏病进程的影响及其相关作用机制。方法:①细胞实验:将大鼠肾小管上皮细胞分为正常对照组(葡萄糖5.5 mmol/L)、高糖组(葡萄糖30 mmol/L)和高渗组(葡萄糖5.5 mmol/L+甘露醇24.5 mmol/L);将100 nmol/L Suz12小干扰RNA(siRNA)及其阴性对照(NC siRNA)转染至高糖培养的肾小管上皮细胞中后48 h,采用Western blotting、CCK-8和流式细胞仪检测Suz12、Ⅳ型胶原蛋白、α-平滑肌肌动蛋白和E-cadherin的蛋白表达、细胞增殖和凋亡。采用染色质免疫共沉淀检测Suz12和金属蛋白酶组织抑制因子3的结合;金属蛋白酶组织抑制因子3表达抑制与组蛋白H3K27me水平增加有关,以甲基化特异性PCR法检测金属蛋白酶组织抑制因子3组蛋白H3K27me3甲基化水平;采用Wnt/β-catenin通路激活剂TDZD-8(10μmol/L,1 h)处理转染Suz12 siRNA的肾小管上皮细胞,以验证Wnt通路的激活是否影响干扰Suz12对细胞损伤的作用。②动物实验:采用腹腔注射60 mg/kg链脲佐菌素构建糖尿病大鼠模型,并通过尾静脉注射0.1 mL含3×108 PFU空腺病毒载体(NC siRNA)或Suz12 siRNA腺病毒(Suz12 siRNA)的PBS;实验结束后收集血清、尿液和肾脏组织,采用全自动生化分析仪检测血糖、血肌酐、尿氮素、尿总蛋白水平;苏木精-伊红和Masson染色观察肾脏组织形态学变化;Western blotting检测肾脏组织中相关蛋白的表达水平。结果与结论:①与正常对照组相比,高糖组肾小管上皮细胞中Suz12、Ⅳ型胶原蛋白和α-平滑肌肌动蛋白蛋白表达水平明显升高,E-cadherin蛋白表达水平明显降低,细胞增殖减少,凋亡率增加;而转染Suz12 siRNA可逆转高糖处理对肾小管上皮细胞的损伤;②与高糖+Suz12 siRNA组相比,TDZD-8处理可逆转Suz12敲低对肾小管上皮细胞中Ⅳ型胶原蛋白、α-平滑肌肌动蛋白、BACKGROUND:Suppressor of Zeste 12(Suz12)can participate in the epithelial-mesenchymal transition of tubular epithelial cells.OBJECTIVE:To investigate the effect of Suz12 on the progression of diabetic nephropathy and its related mechanism.METHODS:(1)Cell experiment:Rat renal tubular epithelial cells were set as normal control group(glucose 5.5 mmol/L),high glucose group(glucose 30 mmol/L),and hypertonic group(glucose 5.5 mmol/L+mannitol 24.5 mmol/L).After transfection of 100 nmol/L Suz12 small interfering RNA(siRNA)and its negative control(NC siRNA)into renal tubular epithelial cells cultured in high glucose,western blot,cell counting kit-8,and flow cytometry were used to detect the protein expression of type IV collagen,Suz12,α-smooth muscle actin,and E-cadherin,cell proliferation and apoptosis,respectively.Subsequently,chromatin immunoprecipitation was used to detect the binding of Suz12 and tissue inhibitor of metalloproteinases-3(TIMP3).The inhibition of TIMP3 expression is associated with the increase of trimethylation of lysine 27 on histone 3(H3K27me).Methylation-specific PCR method was used to detect the methylation level of TIMP3 histone H3K27me3.Renal tubular epithelial cells were treated with Wnt/β-catenin pathway activator TDZD-8(10μmol/L;1 hour)to verify whether the activation of Wnt pathway influences the effects of Suz12 on cell injury.(2)Animal experiment:A diabetic rat model was established by intraperitoneal injection of 60 mg/kg streptozotocin,and then 0.1 mL of PBS solution containing 3×10^(8)PFU empty adenovirus vector(NC siRNA)or Suz12 siRNA adenovirus(Suz12 siRNA)was injected through the tail vein.After the experiment,serum,urine,and kidney tissues were collected,and the contents of blood glucose,serum creatinine,urinary nitrogen and total urinary protein were detected by an automatic biochemical analyzer.Hematoxylin-eosin and Masson staining were used to observe the renal histomorphological changes.Western blot assay was used to detect the expressions of related proteins in kidney tiss

关 键 词：糖尿病肾脏病 Suz12 TIMP3 甲基化 WNT/Β-CATENIN信号通路 

分 类 号：R459.9[医药卫生—治疗学] R318[医药卫生—临床医学] R587.1