背景 增生性玻璃体视网膜病变(PVR)为视网膜表面发生无血管、纤维细胞性增生膜,其发生和发展的具体机制尚未完全阐明.人视网膜色素上皮(hRPE)及血小板源性生长因子(PDGF)在PVR发展中的作用是近几年研究的热点. 目的 探讨缺氧对体外培养hRPE细胞PDGF-BB表达及增生的影响. 方法 hRPE细胞在6孔板中培养,实验组用10、15、20、30、40 μmol/L CoCl2模拟体外培养hRPE细胞的缺氧环境,对照组用未加CoCl2的培养液培养hRPE细胞,采用逆转录PCR(RT-PCR)与ELISA法检测PDGF-BB mRNA和蛋白的表达,采用MTT法检测hRPE细胞增生率.依据转染siRNA的不同将细胞分为PDGF-BB siRNA1组、PDGF-BB siRNA2组、PDGF-BB siRNA3组(为针对PDGF-BB的3条不同的siRNA,其中有一条为有效siRNA)、β-actin siRNA组、无关siRNA组和只加Lip2000的空白对照组.转染4～6h后,除空白对照组外,其余各组加入对细胞PDGF-BB mRNA和蛋白及对hRPE细胞增生影响最明显的15 μmol/L CoCl2模拟细胞缺氧环境24 h,检测PDGF-BB mRNA和蛋白及hRPE细胞增生率. 结果 未加CoCl2的对照组未检测出PDGF-BBmRNA和蛋白的表达,不同浓度CoCl2培养hRPE细胞PDGF-BB mRNA和蛋白的表达量不同,差异均有统计学意义(F=43.737,P＜0.01;F=54.612,P＜0.05),15μmol/L CoCl2组PDGF-BB的表达量最多,与其他各组比较差异均有统计学意义(P＜0.05).MTT检测结果显示,不同浓度CoCl2处理后PDGF-BB蛋白表达及hRPE细胞增生率明显不同,差异均有统计学意义(F=95.379,P＜0.01;F=63.375,P＜0.05),15 μmol/L CoCl2组hRPE细胞增生率明显高于其他浓度组,差异均有统计学意义(P＜0.05),PDGF-BB蛋白表达量与hRPE细胞增生率呈线性正相关(r=0.994,P＜0.05).各细胞转染组hRPE细胞中PDGF-BB mRNA及蛋白的表达整体比较,差异均有统计学意义(F=156.330、125.650,P＜0.01),且PDGF-BB siRNA2组PDGF-BB mRNA较其他各组明显下降,差异均有统计学意义(P＜0.01).MTT检测结果显示,各细胞转染组PDGF-BB蛋白的表达及hRPE细胞增生率明显不同,差异均有统计学意义(F=73.131、98.564,P＜0.01),PDGF-BB siRNA2组PDGF-BB蛋白的表达及细胞增生率与其他各组比较明显下降,差异均有统计学意义(P＜0.05),PDGF-BB蛋白表达与hRPE细胞增生率呈线性正相关(r=0.996,P＜0.05).结论 缺氧能够促进PDGF-BB的表达,PDGF-BB的表达上调可显著促进hRPE细胞的增生.在转染靶向PDGF-BB siRNA后,PDGF-BB的表达受到抑制,可有效降低hRPE细胞的增生率.
揹景 增生性玻璃體視網膜病變(PVR)為視網膜錶麵髮生無血管、纖維細胞性增生膜,其髮生和髮展的具體機製尚未完全闡明.人視網膜色素上皮(hRPE)及血小闆源性生長因子(PDGF)在PVR髮展中的作用是近幾年研究的熱點. 目的 探討缺氧對體外培養hRPE細胞PDGF-BB錶達及增生的影響. 方法 hRPE細胞在6孔闆中培養,實驗組用10、15、20、30、40 μmol/L CoCl2模擬體外培養hRPE細胞的缺氧環境,對照組用未加CoCl2的培養液培養hRPE細胞,採用逆轉錄PCR(RT-PCR)與ELISA法檢測PDGF-BB mRNA和蛋白的錶達,採用MTT法檢測hRPE細胞增生率.依據轉染siRNA的不同將細胞分為PDGF-BB siRNA1組、PDGF-BB siRNA2組、PDGF-BB siRNA3組(為針對PDGF-BB的3條不同的siRNA,其中有一條為有效siRNA)、β-actin siRNA組、無關siRNA組和隻加Lip2000的空白對照組.轉染4～6h後,除空白對照組外,其餘各組加入對細胞PDGF-BB mRNA和蛋白及對hRPE細胞增生影響最明顯的15 μmol/L CoCl2模擬細胞缺氧環境24 h,檢測PDGF-BB mRNA和蛋白及hRPE細胞增生率. 結果 未加CoCl2的對照組未檢測齣PDGF-BBmRNA和蛋白的錶達,不同濃度CoCl2培養hRPE細胞PDGF-BB mRNA和蛋白的錶達量不同,差異均有統計學意義(F=43.737,P＜0.01;F=54.612,P＜0.05),15μmol/L CoCl2組PDGF-BB的錶達量最多,與其他各組比較差異均有統計學意義(P＜0.05).MTT檢測結果顯示,不同濃度CoCl2處理後PDGF-BB蛋白錶達及hRPE細胞增生率明顯不同,差異均有統計學意義(F=95.379,P＜0.01;F=63.375,P＜0.05),15 μmol/L CoCl2組hRPE細胞增生率明顯高于其他濃度組,差異均有統計學意義(P＜0.05),PDGF-BB蛋白錶達量與hRPE細胞增生率呈線性正相關(r=0.994,P＜0.05).各細胞轉染組hRPE細胞中PDGF-BB mRNA及蛋白的錶達整體比較,差異均有統計學意義(F=156.330、125.650,P＜0.01),且PDGF-BB siRNA2組PDGF-BB mRNA較其他各組明顯下降,差異均有統計學意義(P＜0.01).MTT檢測結果顯示,各細胞轉染組PDGF-BB蛋白的錶達及hRPE細胞增生率明顯不同,差異均有統計學意義(F=73.131、98.564,P＜0.01),PDGF-BB siRNA2組PDGF-BB蛋白的錶達及細胞增生率與其他各組比較明顯下降,差異均有統計學意義(P＜0.05),PDGF-BB蛋白錶達與hRPE細胞增生率呈線性正相關(r=0.996,P＜0.05).結論 缺氧能夠促進PDGF-BB的錶達,PDGF-BB的錶達上調可顯著促進hRPE細胞的增生.在轉染靶嚮PDGF-BB siRNA後,PDGF-BB的錶達受到抑製,可有效降低hRPE細胞的增生率.
배경 증생성파리체시망막병변(PVR)위시망막표면발생무혈관、섬유세포성증생막,기발생화발전적구체궤제상미완전천명.인시망막색소상피(hRPE)급혈소판원성생장인자(PDGF)재PVR발전중적작용시근궤년연구적열점. 목적 탐토결양대체외배양hRPE세포PDGF-BB표체급증생적영향. 방법 hRPE세포재6공판중배양,실험조용10、15、20、30、40 μmol/L CoCl2모의체외배양hRPE세포적결양배경,대조조용미가CoCl2적배양액배양hRPE세포,채용역전록PCR(RT-PCR)여ELISA법검측PDGF-BB mRNA화단백적표체,채용MTT법검측hRPE세포증생솔.의거전염siRNA적불동장세포분위PDGF-BB siRNA1조、PDGF-BB siRNA2조、PDGF-BB siRNA3조(위침대PDGF-BB적3조불동적siRNA,기중유일조위유효siRNA)、β-actin siRNA조、무관siRNA조화지가Lip2000적공백대조조.전염4～6h후,제공백대조조외,기여각조가입대세포PDGF-BB mRNA화단백급대hRPE세포증생영향최명현적15 μmol/L CoCl2모의세포결양배경24 h,검측PDGF-BB mRNA화단백급hRPE세포증생솔. 결과 미가CoCl2적대조조미검측출PDGF-BBmRNA화단백적표체,불동농도CoCl2배양hRPE세포PDGF-BB mRNA화단백적표체량불동,차이균유통계학의의(F=43.737,P＜0.01;F=54.612,P＜0.05),15μmol/L CoCl2조PDGF-BB적표체량최다,여기타각조비교차이균유통계학의의(P＜0.05).MTT검측결과현시,불동농도CoCl2처리후PDGF-BB단백표체급hRPE세포증생솔명현불동,차이균유통계학의의(F=95.379,P＜0.01;F=63.375,P＜0.05),15 μmol/L CoCl2조hRPE세포증생솔명현고우기타농도조,차이균유통계학의의(P＜0.05),PDGF-BB단백표체량여hRPE세포증생솔정선성정상관(r=0.994,P＜0.05).각세포전염조hRPE세포중PDGF-BB mRNA급단백적표체정체비교,차이균유통계학의의(F=156.330、125.650,P＜0.01),차PDGF-BB siRNA2조PDGF-BB mRNA교기타각조명현하강,차이균유통계학의의(P＜0.01).MTT검측결과현시,각세포전염조PDGF-BB단백적표체급hRPE세포증생솔명현불동,차이균유통계학의의(F=73.131、98.564,P＜0.01),PDGF-BB siRNA2조PDGF-BB단백적표체급세포증생솔여기타각조비교명현하강,차이균유통계학의의(P＜0.05),PDGF-BB단백표체여hRPE세포증생솔정선성정상관(r=0.996,P＜0.05).결론 결양능구촉진PDGF-BB적표체,PDGF-BB적표체상조가현저촉진hRPE세포적증생.재전염파향PDGF-BB siRNA후,PDGF-BB적표체수도억제,가유효강저hRPE세포적증생솔.
Background Proliferative vitreoretinopathy (PVR):no blood vessels,fibrous membrane cell proliferation occurs retinal surface.The development of specific mechanisms has not been completely clarified,but the retinal pigment epithelium(RPE) and platelet-derived growth factor(PDGF) for the past few years are the research hotspot.Objective To explore the effects of hypoxia on the production of PDGF-BB and proliferation in cultured human RPE (hRPE) cells.Methods In the experimental group,10,15,20,30,40 μmol/L CoCl2 were used to mimic hypoxia environment of hRPE cells,the control group did not add CoCl2 on cultured hRPE cells.By using reverse transcriptive PCR (RT-PCR) and enzyme linked immunosorbent assay(ELISA),the expression of PDGF-BB mRNA and protein was detected,and detected proliferation of hRPE cells by MTT.The cells were divided into 6 groups,different siRNAs were transfected into PDGF-BB siRNA1 group,PDGF-BB siRNA2 group,PDGF-BB siRNA3 group (because PDGF-BB has three different siRNAs,one of which is a valid siRNA),β-actin siRNA group,unrelated sequence siRNA group,only Lip2000 was plused in the blank control group.After transfection of 4-6 hours,except for blank control group,the other five groups were added to PDGF-BB mRNA and protein and its effect on the proliferation of hRPE cells obviously CoCl2 concentrations (15 μmol/L) simulated hypoxia environment of 24 hours,the detection of PDGF-BB mRNA and protein and hRPE cell proliferation rate.Results Neither PDGF-BB mRNA or protein was found in the blank control group.The production of PDGF-BB mRNA and protein in hRPE cells cultured by different concentrations were different,with significant differences among them (F=43.737,P＜0.01;F=54.612,P＜0.05),and the expressions of PDGF-BB mRNA and protein of 15 μmol/L CoCl2 group were more than other groups,with significant differences between the two groups (all at P＜0.05).MTT showed that PDGF-BB protein and hRPE cell proliferation rate in different concentions of CoCl2 groups were different,with significant differences among them(F=95.379,P＜0.01 ; F =63.375,P＜0.05),the expression of PDGF-BB protein was more and hRPE cell proliferation rate was higher in 15 μmol/L CoCl2group than other groups,with significant differences between the two groups (all at P＜0.05),postive correlation was found between PDGF-BB protein and hRPE cell proliferation rate (r =0.994,P＜0.05).The production of PDGF-BB mRNA and protein in the different siRNA transfected groups were different,with significant differences among them (F =156.330,125.650,both at P＜0.01),and the expressions of PDGF-BB mRNA and protein of PDGF-BB siRNA2 group were more than other groups,with significant differences between them(all at P＜0.05).MTT showed that PDGF-BB protein and hRPE cell proliferation rate in different siRNA transfectedgroups were different,with significant differences among them (F =73.131,98.564,both at P＜ 0.01).The expression of PDGF-BB protein was less and hRPE cell proliferation rate was lower in PDGF-BB siRNA2 group than other groups,with significant differences between them (all at P ＜ 0.05),postive correlation was found between PDGF-BB protein and hRPE cell proliferation rate (r =0.996,P＜0.05).Conclusions Proper hypoxia can induce the expression of PDGF-BB,PDGF-BB expression can significantly promote the proliferation of hRPE cells.In the transfection targeting PDGF-BB siRNA,PDGF-BB expression is suppressed,can effectively reduce the value of hRPE cell hyperplasia.
