【摘要】 目的 探讨C1q/肿瘤坏死因子相关蛋白13(CTRP13)通过单磷酸腺苷激活的蛋白激酶/哺乳动物雷帕霉素靶点复合物（AMPK/mTOR）通路对高糖诱导的大鼠原代肝窦内皮细胞（rLSECs）自噬功能的影响。方法 分离、鉴定、培养rLSECs，分为正常对照（NC）组、高糖（HG）组、HG+LV-CTRP13组、HG+慢病毒空载体（LV-Con）组（HG+LV-Con），构建CTRP13慢病毒过表达载体（LV-CTRP13）及慢病毒空载体（LV-Con）并转染r LSECs，分别使用AMPK抑制剂Compound C、mTOR抑制剂Torin1、自噬抑制剂3MA干预，分为HG+LV-Con+Compound C组、HG+LV-CTRP13+Compound C组、HG+LV-Con+Torin1组、HG+LV-CTRP13+Torin1组、HG+LV-Con+3MA、HG+LV-CTRP13+3MA组。透射电子显微镜观察自噬小体，qRT-PCR、Western blot法检测各组CTRP13、自噬相关蛋白Beclin1、人微管相关蛋白轻链3II(LC3II)、人质膜膜泡关联蛋白（PLVAP）及p-AMPK、p-mTOR mRNA和蛋白表达。结果与NC组比较，HG、HG+LV-CTRP13组自噬小体数量降低（P<0.05）。与HG组比较，HG+LV-CTRP13组自噬小体数量升高（P<0.05）。NC、HG+LV-CTRP13组CTRP13 mRNA和蛋白表达高于HG、HG+LV-Con组（P<0.05）。HG+LV-CTRP13组Beclin1、LC3II、p-AMPK、AMPK mRNA表达，Beclin1、LC3II/LC3I蛋白表达高于HG、HG+LV-Con组（P<0.05）,PLVAP、p-mTOR、mTOR mRNA表达，PLVAP蛋白表达低于HG、HG+LV-Con组（P<0.05）。与HG+LV-CTRP13比较，HG+LV-CTRP13+Compound C组p-mTOR蛋白表达升高（P<0.05）,CTRP13、Beclin1、LC3II/LC3I蛋白表达降低（P<0.05）,HG+LV-CTRP13+Torin1组p-AMPK、Beclin1、LC3II/LC3I蛋白表达升高（P<0.05）,CTRP13、p-mTOR蛋白表达降低（P<0.05）,HG+LV-CTRP13+3MA组p-AMPK、p-mTOR、LC3II/LC3I蛋白表达升高（P<0.05）,LC3II/LC3I蛋白表达降低（P<0.05）。结论 CTRP13过表达通过激活AMPK/mTOR信号通路对rLSECs自噬功能发挥保护作用，延缓肝窦毛细血管化。更多还原

【Abstract】 Objective To investigate the effect of C1q/tumor necrosis factor-related protein 13 protein(CTRP13)on the autophagy function of primary rat liver sinusoidal endothelial cells(rLSECs) induced by high glucose through AMP-activated protein kinase/mammalian target of rapamycin complex(AMPK/mTOR)pathway.Methods After isolation,identification and culture,original rat liver sinusoid endothelial cells(rrLSECs)were divided into normal control(NC)group,high glucose(HG)group,HG+LV-CTRP13 group,HG+ lentiviral empty vector(LV-Con)group(HG+LV-Con). CTRP13 lentivirus over expression vector(LV-CTRP13)and lentivirus empty vector(LV-Con)were constructed and transfected into rr LSECs. According to the intervention methods of AMPK inhibitor Compound C,mTOR inhibitor Torin1 and autophagy inhibitor 3MA,the transfected cell were divided into normal control(NC)group,high glucose(HG)group,HG + LV-CTRP13 group,HG + lentiviral empty vector(LV-Con)group(HG +LV-Con). qRT-PCR and western blot were used to detect the mRNA and protein expression levels of CTRP13,autophagy related protein Beclin1,human microtubule-associated protein light chain 3II(LC3II),human plasma membrane membrane vesicle association proteins(PLVAP)and p-AMPK and p-MTOR in rat rLSECs of each group.Results Compared with NC group,the number of autophagosome was decreased in HG and HG+LV-CTRP13 group(P<0. 05). Compared with HG group,the number of autophagosome bodies was increased in HG +LV-CTRP13 group(P<0. 05). The CTRP13 mRNA and protein expression was higher in NC and HG + LV-CTRP13 groups than in HG and HG + LV-Con groups(P<0. 05). In HG+LC-CTRP13 group,Beclin1,LC3II,p-AMPK,and AMPK mRNA,Beclin1,LC3II/LC3I protein expression were higher than HG and HG + LV-Con group(P<0. 05),PLVAP,p-mTOR,mTOR mRNA,and PLVAP protein expression were lower than HG and HG + LV-Con group(P<0. 05).Comparison with HG + LV-CTRP13,p-mTOR protein expression in HG+LV-CTRP13+Compound C group increased(P<0. 05),while expressions of CTRP13,Beclin1 and LC3II/LC3I protein decreased(P<0. 05);the protein expressions of p-AMPK,Beclin1 and LC3II/LC3I were increased in HG+LV+CTRP13 + Torin1 group(P<0. 05),while CTRP13 and p-mTOR protein expression was decreased(P<0. 05);protein expressions of p-AMPK,p-mTOR and LC3II/LC3I were higher in HG+LV-CTRP13+ 3MA group(P<0. 05),while LC3II/LC3I protein expression was lower(P<0. 05).Conclusion CTRP13 overexpression activates AMPK/m TOR-autophagy signaling pathway,which may play a protective role in the function of rLSECs anddelay liver sinusoid capillarization.更多还原