Department of Ophthalmology, Eye and Ear Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Exp Eye Res. 2013 Nov;116:205-18. doi: 10.1016/j.exer.2013.09.010. Epub 2013 Sep 25.
Conditional disruption of Klf4 in the surface ectoderm-derived tissues of the eye results in defective cornea, conjunctiva and the lens. This report describes the effects of disruption of Klf4 in the lens in greater detail. Expression of Klf4, first detected in the embryonic day-12 (E12) mouse lens, peaked at E16 and was decreased in later stages. Early embryonic disruption of Klf4 resulted in a smaller lens with cortical vacuolation and nuclear opacity. Microarray comparison of Klf4CN and WT lens transcriptomes revealed fewer changes in the E16.5 (59 increases, 20 decreases of >1.5-fold) than the PN56 Klf4CN lens (239 increases, 182 decreases of >2-fold). Klf4-target genes in the lens were distinct from those previously identified in the cornea, suggesting disparate functions for Klf4 in these functionally related tissues. Transcripts encoding different crystallins were down-regulated in the Klf4CN lens. Shsp/αB-crystallin promoter activity was stimulated upon co-transfection with pCI-Klf4. Mitochondrial density was significantly higher in the Klf4CN lens epithelial cells, consistent with mitochondrial dysfunction being the most significantly affected pathway within the PN56 Klf4CN lens. The Klf4CN lens contained elevated levels of Alox12 and Alox15 transcripts, less reduced glutathione (GSH) and more oxidized glutathione (GSSG) than the WT, suggesting that it is oxidatively stressed. Although the expression of 2087 genes was modulated during WT lens maturation, transcripts encoding crystallins were abundant at E16.5 and remained stable at PN56. Among the 1065 genes whose expression increased during WT lens maturation, there were 104 Klf4-target genes (9.8%) with decreased expression in the PN56 Klf4CN lens. Taken together, these results demonstrate that Klf4 expression is developmentally regulated in the mouse lens, where it controls the expression of genes associated with lens maturation and redox homeostasis.
条件性敲除眼表外胚层组织中的 Klf4 会导致角膜、结膜和晶状体缺陷。本报告更详细地描述了 Klf4 在晶状体中被敲除的影响。Klf4 的表达最早在胚胎第 12 天(E12)的小鼠晶状体中被检测到,在 E16 时达到峰值,并在后期阶段下降。早期胚胎期 Klf4 的敲除导致晶状体变小,皮质出现空泡化和核混浊。Klf4CN 和 WT 晶状体转录组的微阵列比较显示,E16.5 时的变化较少(59 个增加,20 个减少超过 1.5 倍),而 PN56 Klf4CN 晶状体的变化较多(239 个增加,182 个减少超过 2 倍)。晶状体中的 Klf4 靶基因与先前在角膜中鉴定的基因不同,表明 Klf4 在这些功能相关组织中的功能不同。Klf4CN 晶状体中的不同晶体蛋白编码转录本下调。Shsp/αB-晶体蛋白启动子活性在与 pCI-Klf4 共转染时被刺激。Klf4CN 晶状体上皮细胞中的线粒体密度显著升高,与线粒体功能障碍是 PN56 Klf4CN 晶状体中受影响最显著的途径一致。Klf4CN 晶状体中含有较高水平的 Alox12 和 Alox15 转录本,与 WT 相比,其还原型谷胱甘肽(GSH)减少,氧化型谷胱甘肽(GSSG)增加,表明其处于氧化应激状态。尽管在 WT 晶状体成熟过程中有 2087 个基因的表达被调节,但编码晶体蛋白的转录本在 E16.5 时丰富,并在 PN56 时保持稳定。在 WT 晶状体成熟过程中表达增加的 1065 个基因中,有 104 个 Klf4 靶基因(9.8%)在 PN56 Klf4CN 晶状体中的表达降低。综上所述,这些结果表明,Klf4 在小鼠晶状体中的表达受到发育调控,它控制着与晶状体成熟和氧化还原平衡相关的基因的表达。