国际眼科杂志
國際眼科雜誌
국제안과잡지
INTERNATIONAL JOURNAL OF OPHTHALMOLOGY
2014年
10期
1770-1772
,共3页
柏凌%李鹏%陈凌%何玲%王峰
柏凌%李鵬%陳凌%何玲%王峰
백릉%리붕%진릉%하령%왕봉
微小RNA%白内障%晶状体上皮细胞%细胞凋亡
微小RNA%白內障%晶狀體上皮細胞%細胞凋亡
미소RNA%백내장%정상체상피세포%세포조망
microRNA%cataract%lens epithelium%apoptosis
目的:观察H2 O2处理对晶状体上皮细胞HLE-B3miRNA表达谱的影响,初步明确miRNA在氧化损伤诱导晶状体细胞凋亡中的作用及机制。<br> 方法:100μmol/L H2 O2处理HLE-B324h后,收集细胞用Trizol法提取总RNA。使用芯片检测miRNA的表达,并且qRT-PCR对芯片结果进行验证。运用生物信息学方法预测差异miRNA调控的靶基因。<br> 结果:HLE-B3细胞经H2 O2处理后,28个miRNA表达发生明显变化(18个上调,10个下调)。差异miRNA可能通过调控BCL2 L2和MIP的表达,参与了晶状体细胞凋亡,进而导致了白内障的发生发展。<br> 结论:氧化损伤能够明显改变晶状体上皮细胞的miRNA表达谱,此变化可能在白内障的发生发展中起调节作用。
目的:觀察H2 O2處理對晶狀體上皮細胞HLE-B3miRNA錶達譜的影響,初步明確miRNA在氧化損傷誘導晶狀體細胞凋亡中的作用及機製。<br> 方法:100μmol/L H2 O2處理HLE-B324h後,收集細胞用Trizol法提取總RNA。使用芯片檢測miRNA的錶達,併且qRT-PCR對芯片結果進行驗證。運用生物信息學方法預測差異miRNA調控的靶基因。<br> 結果:HLE-B3細胞經H2 O2處理後,28箇miRNA錶達髮生明顯變化(18箇上調,10箇下調)。差異miRNA可能通過調控BCL2 L2和MIP的錶達,參與瞭晶狀體細胞凋亡,進而導緻瞭白內障的髮生髮展。<br> 結論:氧化損傷能夠明顯改變晶狀體上皮細胞的miRNA錶達譜,此變化可能在白內障的髮生髮展中起調節作用。
목적:관찰H2 O2처리대정상체상피세포HLE-B3miRNA표체보적영향,초보명학miRNA재양화손상유도정상체세포조망중적작용급궤제。<br> 방법:100μmol/L H2 O2처리HLE-B324h후,수집세포용Trizol법제취총RNA。사용심편검측miRNA적표체,병차qRT-PCR대심편결과진행험증。운용생물신식학방법예측차이miRNA조공적파기인。<br> 결과:HLE-B3세포경H2 O2처리후,28개miRNA표체발생명현변화(18개상조,10개하조)。차이miRNA가능통과조공BCL2 L2화MIP적표체,삼여료정상체세포조망,진이도치료백내장적발생발전。<br> 결론:양화손상능구명현개변정상체상피세포적miRNA표체보,차변화가능재백내장적발생발전중기조절작용。
AIM: To identify the changes in microRNA ( miRNA ) profile of human lens epithelium ( HLE) induced by H2 O2 and the role of miRNA in oxidative stress induced apoptosis. <br> METHODS: HLE cell line HLE - B3 was treated by 100μmol/L H2 O2 for 24h and the total RNA were isolated by Trizol reagent. miRNA profile was generated by miRCURYTM LNA microRNA Array. The target genes of differentially expressed miRNAs were predicted by bioinformatics software. <br> RESULTS:Twenty-eight miRNAs showed significantly differential expression after H2 O2 treatment, 18 miRNAs upregulated and 10 miRNAs downregulated. The differentially expressed miRNAs may involve in apoptosis of lens epithetium and development of cataract through targeting BCL2L2 and MIP. <br> CONCLUSION: H2 O2 can induce dramatically changes in miRNA profile of HLE, which may play a pivotal role in the pathogenesis and development of cataract.