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转录因子Pax6和AP-2α相互作用,通过控制基质金属蛋白酶明胶酶B的表达来协调角膜上皮修复。

Transcription Factors Pax6 and AP-2alpha Interact To Coordinate Corneal Epithelial Repair by Controlling Expression of Matrix Metalloproteinase Gelatinase B.

作者信息

Sivak Jeremy M, West-Mays Judith A, Yee Amy, Williams Trevor, Fini M Elizabeth

机构信息

Evelyn F. and William L. McKnight Vision Research Center, Bascom Palmer Eye Institute, University of Miami School of Medicine, Miami, Florida 33136, USA.

出版信息

Mol Cell Biol. 2004 Jan;24(1):245-57. doi: 10.1128/MCB.24.1.245-257.2004.

DOI:10.1128/MCB.24.1.245-257.2004
PMID:14673159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC303332/
Abstract

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.

摘要

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。

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Transcription Factors Pax6 and AP-2alpha Interact To Coordinate Corneal Epithelial Repair by Controlling Expression of Matrix Metalloproteinase Gelatinase B.转录因子Pax6和AP-2α相互作用,通过控制基质金属蛋白酶明胶酶B的表达来协调角膜上皮修复。
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本文引用的文献

1
Deficiency in matrix metalloproteinase gelatinase B (MMP-9) protects against retinal ganglion cell death after optic nerve ligation.基质金属蛋白酶明胶酶B(MMP-9)缺乏可预防视神经结扎后视网膜神经节细胞死亡。
J Biol Chem. 2002 Dec 6;277(49):47461-8. doi: 10.1074/jbc.M204824200. Epub 2002 Sep 26.
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Ectopic expression of AP-2alpha transcription factor in the lens disrupts fiber cell differentiation.AP-2α转录因子在晶状体中的异位表达会破坏纤维细胞分化。
Dev Biol. 2002 May 1;245(1):13-27. doi: 10.1006/dbio.2002.0624.
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MMPs in the eye: emerging roles for matrix metalloproteinases in ocular physiology.眼部的基质金属蛋白酶:基质金属蛋白酶在眼生理中的新作用
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Matrix metalloproteinase gelatinase B (MMP-9) coordinates and effects epithelial regeneration.基质金属蛋白酶明胶酶B(MMP - 9)协调并影响上皮再生。
J Biol Chem. 2002 Jan 18;277(3):2065-72. doi: 10.1074/jbc.M107611200. Epub 2001 Oct 31.
5
Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation properties.一种具有独特DNA结合和反式激活特性的新型小鼠AP-2转录因子AP-2δ的克隆与特性分析。
J Biol Chem. 2001 Nov 2;276(44):40755-60. doi: 10.1074/jbc.M106284200. Epub 2001 Aug 24.
6
Interaction of Maf transcription factors with Pax-6 results in synergistic activation of the glucagon promoter.Maf转录因子与Pax-6的相互作用导致胰高血糖素启动子的协同激活。
J Biol Chem. 2001 Sep 21;276(38):35751-60. doi: 10.1074/jbc.M104523200. Epub 2001 Jul 16.
7
Pax6 and SOX2 form a co-DNA-binding partner complex that regulates initiation of lens development.Pax6和SOX2形成一种共同的DNA结合伴侣复合物,该复合物调节晶状体发育的起始。
Genes Dev. 2001 May 15;15(10):1272-86. doi: 10.1101/gad.887101.
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Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control.AP-2转录因子在脊椎动物发育、细胞凋亡和细胞周期调控中的调节作用。
Gene. 2000 Dec 30;260(1-2):1-12. doi: 10.1016/s0378-1119(00)00454-6.
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Induction of matrix metalloproteinases 2 and 9 following stress to the lens.晶状体应激后基质金属蛋白酶2和9的诱导
Exp Eye Res. 2000 Dec;71(6):591-7. doi: 10.1006/exer.2000.0916.
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Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).对两种常染色体显性遗传小鼠眼部缺陷Ccw和Pax6(coop)进行进一步的基因分析。
Mol Vis. 2000 Oct 31;6:199-203.