中华肾脏病杂志
中華腎髒病雜誌
중화신장병잡지
2009年
10期
788-792
,共5页
刘洁%李英%刘茂东%翟莎娜%张艳玲%张涛%王保兴
劉潔%李英%劉茂東%翟莎娜%張豔玲%張濤%王保興
류길%리영%류무동%적사나%장염령%장도%왕보흥
Megsin%系膜细胞%基因转染%细胞外基质
Megsin%繫膜細胞%基因轉染%細胞外基質
Megsin%계막세포%기인전염%세포외기질
Megsin%Mesangial cell%Gene transfection%Extracellular matrix
目的 观察megsin基因转染对高糖环境中肾小球系膜细胞基质金属蛋白酶2(MMP-2)和组织金属蛋白酶抑制因子2(TIMP-2)的表达及Ⅳ型胶原水平的影响,探讨megsin与系膜细胞增殖和细胞外基质代谢的关系.方法 高糖环境中培养小鼠肾小球系膜细胞,分别于培养12、24、48 h末,应用MTT法检测细胞增殖程度;Western印迹法检测系膜细胞megsin、MMP-2、TIMP-2蛋白表达水平;放免法检测细胞培养上清Ⅳ型胶原浓度.结果 高糖环境中肾小球系膜细胞megsin、TIMP-2表达上调,MMP-2表达下调,细胞增殖明显,细胞上清液中Ⅳ型胶原浓度升高.megsin基因转染后上述,变化趋势更加显著.结论 megsin可诱导系膜细胞增殖,并通过上调TIMP-2、下调MMP-2抑制细胞外基质降解,是加速肾小球硬化的可能机制之一.
目的 觀察megsin基因轉染對高糖環境中腎小毬繫膜細胞基質金屬蛋白酶2(MMP-2)和組織金屬蛋白酶抑製因子2(TIMP-2)的錶達及Ⅳ型膠原水平的影響,探討megsin與繫膜細胞增殖和細胞外基質代謝的關繫.方法 高糖環境中培養小鼠腎小毬繫膜細胞,分彆于培養12、24、48 h末,應用MTT法檢測細胞增殖程度;Western印跡法檢測繫膜細胞megsin、MMP-2、TIMP-2蛋白錶達水平;放免法檢測細胞培養上清Ⅳ型膠原濃度.結果 高糖環境中腎小毬繫膜細胞megsin、TIMP-2錶達上調,MMP-2錶達下調,細胞增殖明顯,細胞上清液中Ⅳ型膠原濃度升高.megsin基因轉染後上述,變化趨勢更加顯著.結論 megsin可誘導繫膜細胞增殖,併通過上調TIMP-2、下調MMP-2抑製細胞外基質降解,是加速腎小毬硬化的可能機製之一.
목적 관찰megsin기인전염대고당배경중신소구계막세포기질금속단백매2(MMP-2)화조직금속단백매억제인자2(TIMP-2)적표체급Ⅳ형효원수평적영향,탐토megsin여계막세포증식화세포외기질대사적관계.방법 고당배경중배양소서신소구계막세포,분별우배양12、24、48 h말,응용MTT법검측세포증식정도;Western인적법검측계막세포megsin、MMP-2、TIMP-2단백표체수평;방면법검측세포배양상청Ⅳ형효원농도.결과 고당배경중신소구계막세포megsin、TIMP-2표체상조,MMP-2표체하조,세포증식명현,세포상청액중Ⅳ형효원농도승고.megsin기인전염후상술,변화추세경가현저.결론 megsin가유도계막세포증식,병통과상조TIMP-2、하조MMP-2억제세포외기질강해,시가속신소구경화적가능궤제지일.
Objective To observe the effects of megsin gene transfection on mesangial cell proliferation and expression of matrix metalloproteinase-2(MMP-2),tissue inhibitor of metalloproteinase-2(TIMP-2)and type IV collagen under high glucose concentration,and to investigate the relationship between megsin and mesangial cell proliferation and extracellular matrix metabolism.Methods Mouse glomerular mesangial cells were cultured in high glucose medium,then cell proliferation was measured by MTT at 12,24 and 48 h respectively after culture.Protein levels of megsin,MMP-2,TIMP-2 in mesangial cells were detected by Western blot.Concentration of type Ⅳ collagen in supernatant of mesangial cells was measured by radioimmunochemistry.Results Under high glucose concentration,megsin and TIMP-2 expression were increased,MMP-2 expression was decreased,the concentration of type Ⅳ collagen in the cellular supernatant was increased,and mesangial cell proliferation was enhanced.After megsin gene transfection,the above changes were more significant.Conclusion Megsin gene induces mesangial cell proliferation and inhibits matrix degradation through TIMP-2 up-regulation and MMP-2 down-regulation,which is probably one of the mechanisms of accelerating glomerulosclerosis.