Sasamoto Yuzuru, Hayashi Ryuhei, Park Sung-Joon, Saito-Adachi Mihoko, Suzuki Yutaka, Kawasaki Satoshi, Quantock Andrew J, Nakai Kenta, Tsujikawa Motokazu, Nishida Kohji
Department of Ophthalmology, Osaka University Medical School, Suita, Osaka 565-0871, Japan.
Department of Stem Cell and Applied Medicine, Osaka University Medical School, Suita, Osaka 565-0871, Japan.
Sci Rep. 2016 Feb 22;6:20807. doi: 10.1038/srep20807.
PAX6 is the key transcription factor involved in eye development in humans, but the differential functions of the two PAX6 isoforms, isoform-a and isoform-b, are largely unknown. To reveal their function in the corneal epithelium, PAX6 isoforms, along with reprogramming factors, were transduced into human non-ocular epithelial cells. Herein, we show that the two PAX6 isoforms differentially and cooperatively regulate the expression of genes specific to the structure and functions of the corneal epithelium, particularly keratin 3 (KRT3) and keratin 12 (KRT12). PAX6 isoform-a induced KRT3 expression by targeting its upstream region. KLF4 enhanced this induction. A combination of PAX6 isoform-b, KLF4, and OCT4 induced KRT12 expression. These new findings will contribute to furthering the understanding of the molecular basis of the corneal epithelium specific phenotype.
PAX6是参与人类眼睛发育的关键转录因子,但两种PAX6亚型,即亚型a和亚型b的不同功能在很大程度上尚不清楚。为了揭示它们在角膜上皮中的功能,将PAX6亚型与重编程因子一起转导到人类非眼部上皮细胞中。在此,我们表明这两种PAX6亚型以不同且协同的方式调节角膜上皮结构和功能特异性基因的表达,特别是角蛋白3(KRT3)和角蛋白12(KRT12)。PAX6亚型a通过靶向其上游区域诱导KRT3表达。KLF4增强了这种诱导作用。PAX6亚型b、KLF4和OCT4的组合诱导KRT12表达。这些新发现将有助于进一步理解角膜上皮特异性表型的分子基础。