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[准分子激光原位角膜磨镶术(LASIK)过程中兔视网膜短暂眼压升高的基因表达谱研究]

[Study on gene expression profiles of rabbit retina transient IOP during LASIK].

作者信息

Zhao Hai-xia, Niu Chun-mei, Guan Wen-ying

机构信息

Department of Ophthalmology, Affiliated Hospital of Inner Mongolia Medical College, NEIMENGGU 010050, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2011 Nov;47(11):1019-24.

Abstract

OBJECTIVE

To detect the changes of gene expression profiles of retina by way of gene chip technology, and to investigate possible molecular pathogenesis of RGCs apoptosis caused by transient high IOP.

METHODS

Twenty-two new Zealand white rabbits were randomized to experimental control and negative pressure suction 3 min groups. The rabbit were executed at different time points of post-LASIK, such as postoperative instant, 7 d, 10 d, then the total RNA of retinal tissue was extracted to detect gene expression profiles by the way of Agilent rabbit one-way gene chip.

RESULTS

Instant after negative pressure suction, the genes differential expressed had 704 genes. Of these, the expression of 485 genes were unregulated and 219 genes down regulated. The higher expression of apoptosis genes were CRYAA, CRYAB, TLR3 and KRT18. 7 d after negative pressure suction, the genes differential expressed had 482 genes. Of these, the expression of 178 genes were unregulated and 304 genes down regulated. The higher expression of apoptosis genes were CRYAB, IL1-BETA and IL1R1. 10 d after negative pressure suction, the genes differential expressed had 402 genes. Of these, the expression of 213 genes were unregulated and 189 genes down regulated. The higher expression of apoptosis genes were CRYAB, CRYBA3, CRYBB2, IL1-BETA and IL1R1.

CONCLUSION

The gene expression had changed after negative pressure suction. The genes with higher fold change protected RGCs from apoptosis.

摘要

目的

采用基因芯片技术检测视网膜基因表达谱的变化,探讨短暂高眼压引起视网膜神经节细胞(RGCs)凋亡的可能分子发病机制。

方法

将22只新西兰白兔随机分为实验对照组和负压吸引3分钟组。在准分子激光原位角膜磨镶术(LASIK)后的不同时间点处死兔子,如术后即刻、7天、10天,然后提取视网膜组织的总RNA,通过安捷伦兔单向基因芯片检测基因表达谱。

结果

负压吸引即刻,差异表达基因有704个。其中,485个基因表达上调,219个基因表达下调。凋亡相关基因CRYAA、CRYAB、TLR3和KRT18表达较高。负压吸引7天后,差异表达基因有482个。其中,178个基因表达上调,304个基因表达下调。凋亡相关基因CRYAB、IL1 - BETA和IL1R1表达较高。负压吸引10天后,差异表达基因有402个。其中,213个基因表达上调,189个基因表达下调。凋亡相关基因CRYAB、CRYBA3、CRYBB2、IL1 - BETA和IL1R1表达较高。

结论

负压吸引后基因表达发生了变化。变化倍数较高的基因可保护RGCs免于凋亡。

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