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Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development

机译:有色上皮细胞中的黑素体在斑马鱼胚胎发育过程中保持晶状体透明性

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摘要

Altered levels of trace elements are associated with increased oxidative stress that is eventually responsible for pathologic conditions. Oxidative stress has been proposed to be involved in eye diseases, including cataract formation. We visualized the distribution of metals and other trace elements in the eye of zebrafish embryos by micro X-ray fluorescence (μ-XRF) imaging. Many elements showed highest accumulation in the retinal pigment epithelium (RPE) of the zebrafish embryo. Knockdown of the zebrafish brown locus homologues tyrp1a/b eliminated accumulation of these elements in the RPE, indicating that they are bound by mature melanosomes. Furthermore, albino (slc45a2) mutants, which completely lack melanosomes, developed abnormal lens reflections similar to the congenital cataract caused by mutation of the myosin chaperon Unc45b, and an in situ spin trapping assay revealed increased oxidative stress in the lens of albino mutants. Finally transplanting a wildtype lens into an albino mutant background resulted in cataract formation. These data suggest that melanosomes in pigment epithelial cells protect the lens from oxidative stress during embryonic development, likely by buffering trace elements.
机译:痕量元素水平的变化与氧化应激的增加有关,氧化应激最终导致病理状况。已经提出氧化应激涉及眼疾病,包括白内障形成。我们通过微X射线荧光(μ-XRF)成像可视化了斑马鱼胚胎眼中金属和其他微量元素的分布。许多元素在斑马鱼胚胎的视网膜色素上皮(RPE)中显示出最高的积累。斑马鱼褐色基因座同源基因tyrp1a / b的敲除消除了RPE中这些元素的积累,表明它们被成熟的黑素体束缚。此外,完全缺乏黑素体的白化病(slc45a2)突变体发生了异常的晶状体反射,类似于由肌球蛋白伴侣Unc45b突变引起的先天性白内障,并且原位自旋阱分析显示白化病突变体的晶状体中氧化应激增加。最后,将野生型晶状体移植到白化突变体背景中,导致白内障形成。这些数据表明,色素上皮细胞中的黑素体在晶状体发育过程中可能通过缓冲微量元素来保护晶状体免受氧化应激。

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