Department of Molecular Biology, Medical Biochemistry and Pathology/Cancer Research Center, Laval University, Québec, QC G1R 2J6, Canada.
J Cell Biol. 2012 Sep 17;198(6):991-8. doi: 10.1083/jcb.201203083. Epub 2012 Sep 10.
Drosophila melanogaster Crumbs (Crb) and its mammalian orthologues (CRB1-3) share evolutionarily conserved but poorly defined roles in regulating epithelial polarity and, in photoreceptor cells, morphogenesis and stability. Elucidating the molecular mechanisms of Crb function is vital, as mutations in the human CRB1 gene cause retinal dystrophies. Here, we report that Crb restricts Rac1-NADPH oxidase-dependent superoxide production in epithelia and photoreceptor cells. Reduction of superoxide levels rescued epithelial defects in crb mutant embryos, demonstrating that limitation of superoxide production is a crucial function of Crb and that NADPH oxidase and superoxide contribute to the molecular network regulating epithelial tissue organization. We further show that reduction of Rac1 or NADPH oxidase activity or quenching of reactive oxygen species prevented degeneration of Crb-deficient retinas. Thus, Crb fulfills a protective role during light exposure by limiting oxidative damage resulting from Rac1-NADPH oxidase complex activity. Collectively, our results elucidate an important mechanism by which Crb functions in epithelial organization and the prevention of retinal degeneration.
果蝇黑色素体 Crumbs(Crb)及其哺乳动物同源物(CRB1-3)在调节上皮细胞极性方面具有进化上保守但定义不明确的作用,并且在光感受器细胞中,还具有形态发生和稳定性的作用。阐明 Crb 功能的分子机制至关重要,因为人类 CRB1 基因突变会导致视网膜营养不良。在这里,我们报告 Crb 限制了上皮细胞和光感受器细胞中 Rac1-NADPH 氧化酶依赖性超氧化物的产生。减少超氧化物水平可挽救 crb 突变体胚胎中的上皮缺陷,表明超氧化物产生的限制是 Crb 的一个关键功能,并且 NADPH 氧化酶和超氧化物有助于调节上皮组织组织的分子网络。我们进一步表明,减少 Rac1 或 NADPH 氧化酶活性或淬灭活性氧可以防止 Crb 缺失的视网膜变性。因此,Crb 通过限制 Rac1-NADPH 氧化酶复合物活性引起的氧化损伤,在光暴露期间发挥保护作用。总之,我们的结果阐明了 Crb 在上皮组织组织和预防视网膜变性中的作用的重要机制。