Chiambaretta Frédéric, Blanchon Loïc, Rabier Bénédicte, Kao Winston W-Y, Liu Janice J, Dastugue Bernard, Rigal Danièle, Sapin Vincent
Department of Ophthalmology, University of Clermont-Ferrand, France.
Invest Ophthalmol Vis Sci. 2002 Nov;43(11):3422-9.
The keratin-12 (K12) protein is essential for the integrity of the corneal epithelium. This study was conducted to investigate the possible involvement of Krüppel-like factor 6 (KLF6) in the corneal regulation of K12 gene expression, in view of the presence of one KLF6 potential binding site in the human K12 promoter and the known role of KLF6 in regulating keratin gene expression.
RT-PCR, Western blot analysis, and immunolocalization experiments were used to investigate the expression of KLF6 mRNA and protein in five human total corneas. The same experimental design was used to explore human corneal epithelial (HCE) cells in 20 patients and a HCE cell line. The ability of the KLF6 protein to modulate K12 promoter activity was studied in the HCE cell line, by transient transfections with a KLF6 expression plasmid and promoter-reporter gene assays. Gel-shift assays were performed to confirm the interactions between the KLF6 protein and specific sequences of the K12 promoter.
The presence of KLF6 transcripts and proteins in human total corneal extracts was demonstrated. Immunohistofluorescence experiments showed positive staining specifically present in the corneal epithelial layer. KLF6 transcripts and proteins were also present in corneal epithelial cells in 20 patients and the HCE cell line. Transient transfections of KLF6 showed statistical transactivation of the K12 promoter in HCE cells. The gel-shift assay showed a physical interaction between KLF6 and the K12 promoter.
The expression of KLF6 in HCE cells and its role in the regulation of K12 gene expression were demonstrated.
角蛋白12(K12)蛋白对于角膜上皮的完整性至关重要。鉴于人类K12启动子中存在一个Krüppel样因子6(KLF6)潜在结合位点以及KLF6在调节角蛋白基因表达方面的已知作用,本研究旨在探讨KLF6在角膜中对K12基因表达的可能调控作用。
采用逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹分析及免疫定位实验,研究KLF6 mRNA和蛋白在5例人全角膜中的表达情况。采用相同的实验设计,对20例患者的人角膜上皮(HCE)细胞及一株HCE细胞系进行研究。通过用KLF6表达质粒进行瞬时转染及启动子-报告基因分析,在HCE细胞系中研究KLF6蛋白调节K12启动子活性的能力。进行凝胶迁移实验以证实KLF6蛋白与K12启动子特定序列之间的相互作用。
证实了人全角膜提取物中存在KLF6转录本和蛋白。免疫组织荧光实验显示,阳性染色特异性地存在于角膜上皮层。KLF6转录本和蛋白也存在于20例患者的角膜上皮细胞及HCE细胞系中。KLF6的瞬时转染显示,HCE细胞中K12启动子有统计学意义的反式激活。凝胶迁移实验显示KLF6与K12启动子之间存在物理相互作用。
证实了KLF6在HCE细胞中的表达及其在K12基因表达调控中的作用。