国际眼科杂志
國際眼科雜誌
국제안과잡지
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY
2010年
5期
827-831
,共5页
杨宏伟%陈晓隆%刘哲丽%刘洁%卜立敏
楊宏偉%陳曉隆%劉哲麗%劉潔%蔔立敏
양굉위%진효륭%류철려%류길%복립민
凋亡%CTGF%视网膜%糖尿病
凋亡%CTGF%視網膜%糖尿病
조망%CTGF%시망막%당뇨병
apoptosis%CTGF%retina%diabetets
目的:探讨CTGF对糖尿病大鼠视网膜内细胞凋亡的影响.方法:将60大鼠分为对照组,糖尿病4,8,12,16wk组和干预组.糖尿病大鼠应用STZ腹腔注射诱导成模.干预组大鼠于糖尿病成模后16wk玻璃体腔注射CTGFsiRNA来造成CTGF基因的沉默.取各组视网膜组织,应用RT-PCR检测视网膜内的CTGF基因表达,Tunnel法检测视网膜凋亡细胞的情况.结果:糖尿病组视网膜内CTGF表达和凋亡细胞数较正常组明显增加.凋亡发生在建模后4wk,并随着时间的延长而加重,在24wk时,凋亡细胞数为25.8个/mm2.CTGF表达于8wk时出现升高,到16wk时升高更明显.CTGFsiRNA处理后凋亡细胞数明显降低.视网膜内CTGF和细胞凋亡之间具有明显的相关性.结论:CTGF参与了糖尿病视网膜早期病变的细胞凋亡机制,CTGFsiRNA有利于改善糖尿病早期视网膜由于凋亡所致的细胞丢失.
目的:探討CTGF對糖尿病大鼠視網膜內細胞凋亡的影響.方法:將60大鼠分為對照組,糖尿病4,8,12,16wk組和榦預組.糖尿病大鼠應用STZ腹腔註射誘導成模.榦預組大鼠于糖尿病成模後16wk玻璃體腔註射CTGFsiRNA來造成CTGF基因的沉默.取各組視網膜組織,應用RT-PCR檢測視網膜內的CTGF基因錶達,Tunnel法檢測視網膜凋亡細胞的情況.結果:糖尿病組視網膜內CTGF錶達和凋亡細胞數較正常組明顯增加.凋亡髮生在建模後4wk,併隨著時間的延長而加重,在24wk時,凋亡細胞數為25.8箇/mm2.CTGF錶達于8wk時齣現升高,到16wk時升高更明顯.CTGFsiRNA處理後凋亡細胞數明顯降低.視網膜內CTGF和細胞凋亡之間具有明顯的相關性.結論:CTGF參與瞭糖尿病視網膜早期病變的細胞凋亡機製,CTGFsiRNA有利于改善糖尿病早期視網膜由于凋亡所緻的細胞丟失.
목적:탐토CTGF대당뇨병대서시망막내세포조망적영향.방법:장60대서분위대조조,당뇨병4,8,12,16wk조화간예조.당뇨병대서응용STZ복강주사유도성모.간예조대서우당뇨병성모후16wk파리체강주사CTGFsiRNA래조성CTGF기인적침묵.취각조시망막조직,응용RT-PCR검측시망막내적CTGF기인표체,Tunnel법검측시망막조망세포적정황.결과:당뇨병조시망막내CTGF표체화조망세포수교정상조명현증가.조망발생재건모후4wk,병수착시간적연장이가중,재24wk시,조망세포수위25.8개/mm2.CTGF표체우8wk시출현승고,도16wk시승고경명현.CTGFsiRNA처리후조망세포수명현강저.시망막내CTGF화세포조망지간구유명현적상관성.결론:CTGF삼여료당뇨병시망막조기병변적세포조망궤제,CTGFsiRNA유리우개선당뇨병조기시망막유우조망소치적세포주실.
·AIM: To detect the effect of CTGF on the apoptosis in the diabetic retina with small interfering RNAs (siRNA) targeting with CTGF. ·METHODS: A total of 60 rats were divided into six groups including control group, diabetic 4,8,12,16 weeks group, and interference group. Diabetic rats were induced by STZ intra-peritoneal. At 4, 8, 12, 16 weeks after diabetic setting up, retinas were obtained from control, diabetic rats and diabetic animals treated by intravitreal injection of CTGFsiRNA to suppress the expression of CTGF mRNA. Retinal cells apoptosis was detected by Tunnel staining and mRNA expression of CTGF was analyzed by RT-PCR.·RESULTS: The levels of CTGF and the apoptosis in the retinas of diabetic rats were significantly higher than those in the controls. Apoptosis occurred at 4 weeks after a diabetic model setting up, became serious with the diabetes developing, while CTGF elevated at 8 weeks. The cell apoptosis counts increased to 25.8cells/mm2 at 24 weeks of diabetes. SiRNA-mediated inhibition of CTGF mRNA resulted in a significant decrease in apoptosis. Significant correlations were found between CTGF and apoptosis in the retina.·CONCLUSION: These results suggest that CTGF might be involved in retinal cells apoptosis which is a characteristic of early diabetic retina. siRNA targeting CTGF seems to have the advantage of ameliorating retinal cells lost.