Capowski Elizabeth E, Wright Lynda S, Liang Kun, Phillips M Joseph, Wallace Kyle, Petelinsek Anna, Hagstrom Anna, Pinilla Isabel, Borys Katarzyna, Lien Jessica, Min Jee Hong, Keles Sunduz, Thomson James A, Gamm David M
Waisman Center, University of Wisconsin-Madison, Madison, WI, 53705, USA.
McPherson Eye Research Institute, University of Wisconsin-Madison, Madison, WI, 53705, USA.
Stem Cells. 2016 Nov;34(11):2625-2634. doi: 10.1002/stem.2414. Epub 2016 Jul 5.
Few gene targets of Visual System Homeobox 2 (VSX2) have been identified despite its broad and critical role in the maintenance of neural retina (NR) fate during early retinogenesis. We performed VSX2 ChIP-seq and ChIP-PCR assays on early stage optic vesicle-like structures (OVs) derived from human iPS cells (hiPSCs), which highlighted WNT pathway genes as direct regulatory targets of VSX2. Examination of early NR patterning in hiPSC-OVs from a patient with a functional null mutation in VSX2 revealed mis-expression and upregulation of WNT pathway components and retinal pigmented epithelium (RPE) markers in comparison to control hiPSC-OVs. Furthermore, pharmacological inhibition of WNT signaling rescued the early mutant phenotype, whereas augmentation of WNT signaling in control hiPSC-OVs phenocopied the mutant. These findings reveal an important role for VSX2 as a regulator of WNT signaling and suggest that VSX2 may act to maintain NR identity at the expense of RPE in part by direct repression of WNT pathway constituents. Stem Cells 2016;34:2625-2634.
尽管视系统同源框2(VSX2)在视网膜早期发育过程中对维持神经视网膜(NR)命运起着广泛且关键的作用,但其基因靶点却鲜有被鉴定出来。我们对源自人诱导多能干细胞(hiPSC)的早期视泡样结构(OV)进行了VSX2染色质免疫沉淀测序(ChIP-seq)和染色质免疫沉淀聚合酶链反应(ChIP-PCR)分析,结果表明WNT信号通路基因是VSX2的直接调控靶点。对一名VSX2功能缺失突变患者的hiPSC-OV中的早期NR模式进行检测发现,与对照hiPSC-OV相比,WNT信号通路成分和视网膜色素上皮(RPE)标志物存在表达错误和上调的情况。此外,WNT信号的药理学抑制挽救了早期突变表型,而在对照hiPSC-OV中增强WNT信号则模拟了突变表型。这些发现揭示了VSX2作为WNT信号调节因子的重要作用,并表明VSX2可能部分通过直接抑制WNT信号通路成分来以牺牲RPE为代价维持NR特性。《干细胞》2016年;34卷:2625 - 2634页