Sivak Jeremy M, West-Mays Judith A, Yee Amy, Williams Trevor, Fini M Elizabeth
Evelyn F. and William L. McKnight Vision Research Center, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33136, USA.
Mol Cell Biol. 2004 Jan;24(1):245-57. doi: 10.1128/MCB.24.1.245-257.2004.
Pax6 is a paired box containing transcription factor that resides at the top of a genetic hierarchy controlling eye development. It continues to be expressed in tissues of the adult eye, but its role in this capacity is unclear. Pax6 is present in the adult corneal epithelium, and we showed that the amount of Pax6 is increased at the migrating front as the epithelium resurfaces the cornea after injury. We also showed that Pax6 controls activity of the transcriptional promoter for the matrix metalloproteinase, gelatinase B (gelB; MMP-9) in cell culture transfection studies. gelB expression is turned on at the migrating epithelial front in the cornea, and it coordinates and effects aspects of epithelial regeneration. We define here two positively acting Pax6 response elements in the gelB promoter. Pax6 binds directly to one of these sites through the paired DNA-binding domain. It binds the second site indirectly by interaction with AP-2alpha, a transcription factor that also exerts control over eye development. Pax6 control of gelB expression was examined in vivo by using a corneal reepithelialization model in mice heterozygous for a Pax6 paired-domain mutation (Sey(+/-)). A reduced Pax6 dosage in these mice resulted in a loss of gelB expression at the migrating epithelial front. This effect was correlated with an increase in inflammation and the rate of reepithelialization, a finding consistent with the phenotype of gelB knockout mice. Together, these data indicate that Pax6 controls activity of the gelB promoter through cooperative interactions with AP-2alpha and support an active role for Pax6 in maintenance and repair of the adult corneal epithelium.
Pax6是一种含有配对盒的转录因子,处于控制眼睛发育的遗传层级的顶端。它在成年眼睛的组织中持续表达,但其在这一功能中的作用尚不清楚。Pax6存在于成年角膜上皮中,我们发现,在角膜受伤后上皮重新覆盖角膜时,迁移前沿的Pax6量会增加。我们还在细胞培养转染研究中表明,Pax6控制基质金属蛋白酶明胶酶B(gelB;MMP-9)转录启动子的活性。gelB在角膜迁移的上皮前沿开启表达,并协调和影响上皮再生的各个方面。我们在此确定了gelB启动子中的两个正向作用的Pax6反应元件。Pax6通过配对DNA结合域直接与其中一个位点结合。它通过与AP-2α相互作用间接结合第二个位点,AP-2α也是一种对眼睛发育有调控作用的转录因子。通过使用Pax6配对域突变(Sey(+/-))杂合子小鼠的角膜再上皮化模型,在体内研究了Pax6对gelB表达的控制。这些小鼠中Pax6剂量的减少导致迁移上皮前沿的gelB表达缺失。这种效应与炎症增加和再上皮化速率加快相关,这一发现与gelB基因敲除小鼠的表型一致。总之,这些数据表明,Pax6通过与AP-2α的协同相互作用控制gelB启动子的活性,并支持Pax6在成年角膜上皮的维持和修复中发挥积极作用。