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作 者:崔晓栋[1] 尹青令[2] 张晓芸[1] 李宏[1] 官秀梅[1] 李鑫[1] 王建英[1] 成敏[2]
机构地区:[1]潍坊医学院基础医学院,山东省潍坊市261053 [2]潍坊医学院医学中心实验室,山东省潍坊市261053
出 处:《世界华人消化杂志》2012年第32期3135-3139,共5页World Chinese Journal of Digestology
基 金:国家自然科学基金资助项目;No.30900290;山东省自然科学基金资助项目;No.ZR2010HQ046~~
摘 要:目的:探讨不同大小的流体剪切应力对大鼠肝星状细胞株HSC-T6的活化和基因表达的影响.方法:对种植于鼠尾胶原上的HSC-T6细胞施以剪切应力处理,剪切应力的大小分别为6、12、20dyn/cm2,干预时间为3h.TRIzol法提取mRNA,采用SYBR Green荧光定量RT-PCR方法分别检测各组-SMA、Collogen-Ⅰ、Collogen-Ⅲ、MMP-2及MMP-9基因的表达情况,流式细胞术检测细胞内蛋白-SMA的表达.结果:剪切应力处理3h后,与对照组相比,6dyn/cm2剪切应力组-SMA、Collogen-Ⅲ的表达降低,但随着剪切应力的增加(12dyn/cm2、20dyn/cm2),-SMAmRNA较对照组表达升高;20dyn/cm2剪切应力组Collogen-Ⅲ基因表达较对照组升高;3种剪切应力组之间Collogen-ⅠmRNA的表达无统计学差异;3种剪切应力均上调MMP-2mRNA的表达.结论:低剪切应力对HSC-T6的活化有一定的抑制作用,相反高剪切应力可以促进HSC-T6的活化,促进Collogen-Ⅲ、MMP-2的表达.AIM:To investigate the effects of different types of fluid shear stress on the activation of hepatic stellate cells-T6(HSC-T6) and expression of-SMA,collogen-Ⅰ,collogen-Ⅲ,MMP-2,and MMP-9.METHODS:HSC-T6 cells were seeded on slides precoated with rat tail collagen and exposedto different types of fluid shear stress(6,12,20 dyn/cm2) for 3 h,and static cells served as controls.The gene expression of-SMA,collogen-Ⅰ,collogen-Ⅲ,MMP-2 and MMP-9 was assayed by real-time RT-PCR.Intracellular-SMA protein was analyzed by FACS.RESULTS:After treatment by fluid shear stress,the expression of-SMA and collogen-Ⅲ was lower in the low shear stress(6 dyn/cm2) group than that in the control group.However,the expression of-SMA was higher in the moderate(12 dyn/cm2) and high(20 dyn/cm2) shear stress groups than that in the control group,and the expression of collogen-Ⅲ was higher in the high shear stress group than that in the control group.There was no significant difference in the expression of collogen-Ⅰ among different fluid shear stress groups.The expression of MMP-2 was higher that in three fluid shear stress groups than in the control group.CONCLUSION:High fluid shear stress can lead to the activation of HSC-T6 cells and promote the mRNA expression of-SMA,collogen-Ⅲ and MMP-2.
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