山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2015年
18期
4-6
,共3页
戚勋%苑永辉%钟红珊%徐克
慼勛%苑永輝%鐘紅珊%徐剋
척훈%원영휘%종홍산%서극
2-羟丙基-β-环糊精%脐静脉内皮细胞%细胞迁移%细胞增殖%血管新生
2-羥丙基-β-環糊精%臍靜脈內皮細胞%細胞遷移%細胞增殖%血管新生
2-간병기-β-배호정%제정맥내피세포%세포천이%세포증식%혈관신생
2-hydroxypropyl-β-cyclodextrin%umbilical vein endothelial cells%cell migration%cell proliferation%an-giogenesis
目的:探讨2-羟丙基-β-环糊精(2HP-β-CD)对人脐静脉内皮细胞(HUVEC)体外增殖和迁移的作用。方法体外培养HUVEC,分为两组,实验组分别加入浓度为10-10、10-9、10-8、10-7、10-6、10-5 mol/L的2HP-β-CD,空白组加入含0.5%FBS的等量培养液。采用CCK-8法检测各组细胞增殖活力,改良Boyden Chamber法检测各组细胞的迁移能力。结果实验组中,加入10-10、10-9、10-8 mol/L 2HP-β-CD者的OD450分别为空白组的1.4、1.6、1.7倍,10-8 mol/L 2 HP-β-CD增强细胞增殖活力的作用最明显( P均<0.01);加入10-7、10-6、10-5 mol/L 2 HP-β-CD者的OD450与空白组比较差异无统计学意义。加入10-9及10-8 mol/L 2HP-β-CD者细胞迁移数显著高于空白组(P均<0.05),其他浓度组细胞迁移数与空白组比较差异均无统计学意义。结论适当浓度的2HP-β-CD可促进HUVEC的增殖和迁移。
目的:探討2-羥丙基-β-環糊精(2HP-β-CD)對人臍靜脈內皮細胞(HUVEC)體外增殖和遷移的作用。方法體外培養HUVEC,分為兩組,實驗組分彆加入濃度為10-10、10-9、10-8、10-7、10-6、10-5 mol/L的2HP-β-CD,空白組加入含0.5%FBS的等量培養液。採用CCK-8法檢測各組細胞增殖活力,改良Boyden Chamber法檢測各組細胞的遷移能力。結果實驗組中,加入10-10、10-9、10-8 mol/L 2HP-β-CD者的OD450分彆為空白組的1.4、1.6、1.7倍,10-8 mol/L 2 HP-β-CD增彊細胞增殖活力的作用最明顯( P均<0.01);加入10-7、10-6、10-5 mol/L 2 HP-β-CD者的OD450與空白組比較差異無統計學意義。加入10-9及10-8 mol/L 2HP-β-CD者細胞遷移數顯著高于空白組(P均<0.05),其他濃度組細胞遷移數與空白組比較差異均無統計學意義。結論適噹濃度的2HP-β-CD可促進HUVEC的增殖和遷移。
목적:탐토2-간병기-β-배호정(2HP-β-CD)대인제정맥내피세포(HUVEC)체외증식화천이적작용。방법체외배양HUVEC,분위량조,실험조분별가입농도위10-10、10-9、10-8、10-7、10-6、10-5 mol/L적2HP-β-CD,공백조가입함0.5%FBS적등량배양액。채용CCK-8법검측각조세포증식활력,개량Boyden Chamber법검측각조세포적천이능력。결과실험조중,가입10-10、10-9、10-8 mol/L 2HP-β-CD자적OD450분별위공백조적1.4、1.6、1.7배,10-8 mol/L 2 HP-β-CD증강세포증식활력적작용최명현( P균<0.01);가입10-7、10-6、10-5 mol/L 2 HP-β-CD자적OD450여공백조비교차이무통계학의의。가입10-9급10-8 mol/L 2HP-β-CD자세포천이수현저고우공백조(P균<0.05),기타농도조세포천이수여공백조비교차이균무통계학의의。결론괄당농도적2HP-β-CD가촉진HUVEC적증식화천이。
Objective To investigate the effect of 2-hydroxypropyl-β-cyclodextrin (2HP-β-CD) on the migration and proliferation of human umbilical vein endothelial cells ( HUVECs) in vitro.Methods HUVECs were cultured in vitro and were divided into two groups:the experimental group and the blank group .HUVECs in the experimental group were treated with different concentrations of 2HP-β-CD (10 -10-10 -5 mol/L), and the same amount of 0.5% FBS was added into the blank group .CCK-8 was used to detect the cell proliferation activities of the two groups , and the modified Boyden Chamber was applied to observe the cell migration in each group .Results The OD450 of the experimental group which was added with 10 -10 mol/L, 10 -9 mol/L and 10 -8 mol/L 2HP-β-CD was 1.4, 1.6 and 1.7 times higher than that of the blank group;and 10 -10 mol/L 2HP-β-CD had the most significant effect in promoting the proliferation of HUVECs ( all P <0.01).No significant difference was found in OD450 of the two groups when we added 10 -7, 10 -6 and 10 -5 mol/L 2HP-β-CD to HUVECs.The migration of HUVECs which were added with 2HP-β-CD at the concentration of 10 -9 mol/L and 10 -8 mol/L in the experimental group was significantly higher than that of the blank group (all P<0.05).When we added other concentrations of 2HP-β-CD, no significant difference was found in the cell migration between the experimental and blank groups.Conclusion Suitable concentrations of 2HP-β-CD can promote the migration and proliferation of HUVECs .