中华内分泌代谢杂志
中華內分泌代謝雜誌
중화내분비대사잡지
CHINESE JOURNAL OF ENDOCRINOLOGY AND METABOLISM
2014年
5期
428-431
,共4页
褚月颉%王鹏华%李代清%于德民
褚月頡%王鵬華%李代清%于德民
저월힐%왕붕화%리대청%우덕민
Amot%血管内皮细胞%高糖%缺氧%血管新生
Amot%血管內皮細胞%高糖%缺氧%血管新生
Amot%혈관내피세포%고당%결양%혈관신생
Amot%Vascular endothelial cells%High glucose%Anoxia%Angiogenesis
目的 观察高糖和缺氧对血管内皮细胞(VECs) Amot表达的影响,并探讨该蛋白在血管新生中的作用.方法 VECs以不同浓度葡萄糖培养48 h后,再分别在正常氧或缺氧条件下培养24h,以Western印迹法测定p130-Amot和p80-Amot的蛋白表达.用siRNA下调Amot的蛋白表达,采用划痕实验及血管生成实验评价该蛋白表达下降对血管新生功能的影响.结果 p130-Amot在正糖(5.5 mmol/L)常氧组和正糖缺氧组明显高于高糖(30 mmol/L)常氧组、高糖缺氧组、中糖(15 mmol/L)常氧组和中糖缺氧组(均P<0.01),而正糖常氧组比正糖缺氧组更高(P<0.01).p80-Amot在各组间的表达差异无统计学意义(P>0.05).用siRNA技术下调Amot蛋白表达后,VECs迁移能力和血管生成能力较正常细胞明显减弱.结论 高糖比缺氧更显著降低VECs Amot蛋白的表达,该蛋白表达的下降明显抑制VECs新生血管的形成.
目的 觀察高糖和缺氧對血管內皮細胞(VECs) Amot錶達的影響,併探討該蛋白在血管新生中的作用.方法 VECs以不同濃度葡萄糖培養48 h後,再分彆在正常氧或缺氧條件下培養24h,以Western印跡法測定p130-Amot和p80-Amot的蛋白錶達.用siRNA下調Amot的蛋白錶達,採用劃痕實驗及血管生成實驗評價該蛋白錶達下降對血管新生功能的影響.結果 p130-Amot在正糖(5.5 mmol/L)常氧組和正糖缺氧組明顯高于高糖(30 mmol/L)常氧組、高糖缺氧組、中糖(15 mmol/L)常氧組和中糖缺氧組(均P<0.01),而正糖常氧組比正糖缺氧組更高(P<0.01).p80-Amot在各組間的錶達差異無統計學意義(P>0.05).用siRNA技術下調Amot蛋白錶達後,VECs遷移能力和血管生成能力較正常細胞明顯減弱.結論 高糖比缺氧更顯著降低VECs Amot蛋白的錶達,該蛋白錶達的下降明顯抑製VECs新生血管的形成.
목적 관찰고당화결양대혈관내피세포(VECs) Amot표체적영향,병탐토해단백재혈관신생중적작용.방법 VECs이불동농도포도당배양48 h후,재분별재정상양혹결양조건하배양24h,이Western인적법측정p130-Amot화p80-Amot적단백표체.용siRNA하조Amot적단백표체,채용화흔실험급혈관생성실험평개해단백표체하강대혈관신생공능적영향.결과 p130-Amot재정당(5.5 mmol/L)상양조화정당결양조명현고우고당(30 mmol/L)상양조、고당결양조、중당(15 mmol/L)상양조화중당결양조(균P<0.01),이정당상양조비정당결양조경고(P<0.01).p80-Amot재각조간적표체차이무통계학의의(P>0.05).용siRNA기술하조Amot단백표체후,VECs천이능력화혈관생성능력교정상세포명현감약.결론 고당비결양경현저강저VECs Amot단백적표체,해단백표체적하강명현억제VECs신생혈관적형성.
Objective To observe the effects of high glucose and anoxia on Amot expression in vascular endothelial cells (VECs),and explore its role in angiogenesis.Methods VECs were incubated with different glucose concentrations for 48 h,and then cultured at normal oxygen concentration or anaerobic condition for 24 h.The protein expressions of p130-Amot and p80-Amot were detected by Western blot.After Amot expression was downregulated in VECs by siRNA,wound healing experiments and angiogenesis experiments were performed to test the effect of decreased Amot expression on angiogenesis.Results pl30-Amot protein expressions in low glucose (5.5mmol/L) plus normal oxygen group and low glucose plus anaerobic group were higher than those in high glucose (30mmol/L) plus normal oxygen group,high glucose plus anaerobic group,middle glucose (15 mmol/L) plus normal oxygen group,and middle glucose plus anaerobic group (all P<0.01).Compared with low glucose plus anaerobic group,p130-Amot expression was higher in low glucose plus normal oxygen group (P < 0.01).However,the expression of p80-Amot showed no statistically significant difference among different groups (P>0.05).Compared to the normal VECs,the cells with decreased Amot expression by siRNA exhibited an attenuated cell migration in the wound healing experiments and a lesser tube formation in the angiogenesis experiments.Conclusions High glucose exerts a more significantly negtive effect on the Amot expression than anoxia in VECs.The downregulation of Amot expression inhibits migration and angiogenesis of VECs.