中华眼科杂志
中華眼科雜誌
중화안과잡지
Chinese Journal of Ophthalmology
2012年
4期
337-343
,共7页
凌士奇%黎韦华%梁凌毅%徐建刚%邝文辉
凌士奇%黎韋華%樑凌毅%徐建剛%鄺文輝
릉사기%려위화%량릉의%서건강%광문휘
角膜移植%角膜%淋巴管生成%大鼠
角膜移植%角膜%淋巴管生成%大鼠
각막이식%각막%림파관생성%대서
Corneal transplantation%Cornea%Lymphangiogenesis%Rats
目的 研究大鼠角膜移植后角膜新生淋巴管的动态变化及其与血管内皮生长因子C(VEGF-C)、炎症指数间的关系.方法 实验研究.制备大鼠角膜移植模型,于移植后第1、3、7、10、14、30、60天通过免疫组织化学染色和全角膜免疫荧光法标记角膜新生淋巴管,并进行淋巴管计数(LVC),检测淋巴管的动态变化;运用免疫组织化学染色、酶联免疫吸附测定(ELISA)、实时荧光定量PCR法检测角膜组织中VEGF-C的蛋白和mRNA的变化;同时记录炎症指数以评估角膜移植后的炎症反应.运用配对t检验比较角膜移植后3d和14 d时VEGF-C mRNA的差异,Pearson相关分析检验LVC和炎症指数、LVC和VEGF-C之间的关联.结果 免疫组织化学染色提示角膜移植后3d角膜基质中出现了新生淋巴管,LVC为(1.8±0.3)个,14 d时达到高峰,为(9.1±1.5)个.角膜移植后VEGF-C的分泌迅速增加,3d时达到第1个高峰,VEGF-C mRNA为(1.62±0.08) copies/g,以后逐渐减少,7d时角膜基质中几乎无VEGF-C的表达,继而VEGF-C的分泌再次增加,14 d时达到第2个高峰,VEGF-C mRNA为(2.48±0.03) copies/g,与3d时比较,两者之间差异有统计学意义(t=4.296,P =0.020).LVC与VEGF-C、炎症指数间相关系数有统计学意义(r=0.51,P=0.003和r=0.55,P=0.003).结论 角膜移植后角膜新生淋巴管与VEGF-C及炎症指数间密切相关.
目的 研究大鼠角膜移植後角膜新生淋巴管的動態變化及其與血管內皮生長因子C(VEGF-C)、炎癥指數間的關繫.方法 實驗研究.製備大鼠角膜移植模型,于移植後第1、3、7、10、14、30、60天通過免疫組織化學染色和全角膜免疫熒光法標記角膜新生淋巴管,併進行淋巴管計數(LVC),檢測淋巴管的動態變化;運用免疫組織化學染色、酶聯免疫吸附測定(ELISA)、實時熒光定量PCR法檢測角膜組織中VEGF-C的蛋白和mRNA的變化;同時記錄炎癥指數以評估角膜移植後的炎癥反應.運用配對t檢驗比較角膜移植後3d和14 d時VEGF-C mRNA的差異,Pearson相關分析檢驗LVC和炎癥指數、LVC和VEGF-C之間的關聯.結果 免疫組織化學染色提示角膜移植後3d角膜基質中齣現瞭新生淋巴管,LVC為(1.8±0.3)箇,14 d時達到高峰,為(9.1±1.5)箇.角膜移植後VEGF-C的分泌迅速增加,3d時達到第1箇高峰,VEGF-C mRNA為(1.62±0.08) copies/g,以後逐漸減少,7d時角膜基質中幾乎無VEGF-C的錶達,繼而VEGF-C的分泌再次增加,14 d時達到第2箇高峰,VEGF-C mRNA為(2.48±0.03) copies/g,與3d時比較,兩者之間差異有統計學意義(t=4.296,P =0.020).LVC與VEGF-C、炎癥指數間相關繫數有統計學意義(r=0.51,P=0.003和r=0.55,P=0.003).結論 角膜移植後角膜新生淋巴管與VEGF-C及炎癥指數間密切相關.
목적 연구대서각막이식후각막신생림파관적동태변화급기여혈관내피생장인자C(VEGF-C)、염증지수간적관계.방법 실험연구.제비대서각막이식모형,우이식후제1、3、7、10、14、30、60천통과면역조직화학염색화전각막면역형광법표기각막신생림파관,병진행림파관계수(LVC),검측림파관적동태변화;운용면역조직화학염색、매련면역흡부측정(ELISA)、실시형광정량PCR법검측각막조직중VEGF-C적단백화mRNA적변화;동시기록염증지수이평고각막이식후적염증반응.운용배대t검험비교각막이식후3d화14 d시VEGF-C mRNA적차이,Pearson상관분석검험LVC화염증지수、LVC화VEGF-C지간적관련.결과 면역조직화학염색제시각막이식후3d각막기질중출현료신생림파관,LVC위(1.8±0.3)개,14 d시체도고봉,위(9.1±1.5)개.각막이식후VEGF-C적분비신속증가,3d시체도제1개고봉,VEGF-C mRNA위(1.62±0.08) copies/g,이후축점감소,7d시각막기질중궤호무VEGF-C적표체,계이VEGF-C적분비재차증가,14 d시체도제2개고봉,VEGF-C mRNA위(2.48±0.03) copies/g,여3d시비교,량자지간차이유통계학의의(t=4.296,P =0.020).LVC여VEGF-C、염증지수간상관계수유통계학의의(r=0.51,P=0.003화r=0.55,P=0.003).결론 각막이식후각막신생림파관여VEGF-C급염증지수간밀절상관.
Objective To study the development of lymphatic vessels after keratoplasty and to explore the molecular mechanisms of corneal lymphangiogenesis in transplanted corneas. Methods Experimental research.The development of corneal lymphangiogenesis was examined by LYVE-1immunohistochemistry and whole mount immunofluorescence 1,3,7,10,14,30 and 60 days after corneal transplantation, then lymphatic vessels counting (LVC)was evaluated. The expression of vascular endothelial growth factor-C (VEGF-C) in transplanted corneas was examined by immunohistochemistry,enzyme-linked immunosorbent assay (ELISA), and real time-PCR at same time. In addition, the inflammatory index (IF) was recorded at each time point.The association of VEGF-C and IF with LVC in transplanted corneas was examined. Analysis of the significance of differences between two groups was performed using paired Student's t-test. Pearson's analysis was used to analyze the correlation between VEGF-C,IF and LVC.Results Corneal lymphangiogenesis occurred in the stroma with LVC ( 1.8 ± 0.3)on Day 3,then developed and reached the peak with LVC (9.1 ± 1.5) on Day 14 after corneal transplantation.Both VEGF-C protein and mRNA up-regulated dramatically in rat transplanted corneas.The immunoreactivity reached the peak on the 3rd day and the 14th day after keratoplasty.Compared with the expression of VEGF-C mRNA ( 1.62 ± 0.08 copies/g) on Day 3,the expression of VEGF-C mRNA (2.48 ±0.03 copies/g) significantly increased 14 days after the transplantation ( t =4.296,P =0.02 ).LVC was strongly and positively correlated with IF ( r =0.55,P =0.003 ) and the expression of VEGF-C mRNA ( r =0.51,P =0.003 ). Conclusions Corneal lymphangiogenesis correlates closely with corneal inflammation.The increased expression of VEGF-C in the cornea may be one of the important molecular mechanisms in the occurrence of corneal lymphangiogenesis after keratoplasty.