Department of Biology, Integrated Sciences Complex, University of Massachusetts Boston, Boston, USA.
Department of Biology, Integrated Sciences Complex, University of Massachusetts Boston, Boston, USA.
Dev Biol. 2021 Aug;476:68-78. doi: 10.1016/j.ydbio.2021.03.013. Epub 2021 Mar 25.
Vitamin A deficiency can cause human pathologies that range from blindness to embryonic malformations. This diversity is due to the lack of two major vitamin A metabolites with very different functions: the chromophore 11-cis-retinal (vitamin A aldehyde) is a critical component of the visual pigment that mediates phototransduction, while the signaling molecule all-trans-retinoic acid regulates the development of various tissues and is required for the function of the immune system. Since animals cannot synthesize vitamin A de novo, they must obtain it either as preformed vitamin A from animal products or as carotenoid precursors from plant sources. Due to its essential role in the visual system, acute vitamin A deprivation impairs photoreceptor function and causes night blindness (poor vision under dim light conditions), while chronic deprivation results in retinal dystrophies and photoreceptor cell death. Chronic vitamin A deficiency is the leading cause of preventable childhood blindness according to the World Health Organization. Due to the requirement of vitamin A for retinoic acid signaling in development and in the immune system, vitamin A deficiency also causes increased mortality in children and pregnant women in developing countries. Drosophila melanogaster is an excellent model to study the effects of vitamin A deprivation on the eye because vitamin A is not essential for Drosophila development and chronic deficiency does not cause lethality. Moreover, genetic screens in Drosophila have identified evolutionarily conserved factors that mediate the production of vitamin A and its cellular uptake. Here, we review our current knowledge about the role of vitamin A in the visual system of mammals and Drosophila melanogaster. We compare the molecular mechanisms that mediate the uptake of dietary vitamin A precursors and the metabolism of vitamin A, as well as the consequences of vitamin A deficiency for the structure and function of the eye.
维生素 A 缺乏可导致人体出现各种病变,从失明到胚胎畸形均有涉及。这种多样性源于两种主要维生素 A 代谢物的缺乏,它们的功能差异巨大:生色团 11-顺式视黄醛(维生素 A 醛)是介导光转导的视觉色素的关键成分,而信号分子全反式视黄酸则调节各种组织的发育,是免疫系统功能所必需的。由于动物不能从头合成维生素 A,它们必须从动物产品中获取已形成的维生素 A,或者从植物来源中获取类胡萝卜素前体。由于其在视觉系统中的重要作用,急性维生素 A 缺乏会损害感光器的功能,导致夜盲症(在昏暗光线下视力不佳),而慢性缺乏则会导致视网膜营养不良和感光细胞死亡。根据世界卫生组织的说法,慢性维生素 A 缺乏是可预防的儿童失明的主要原因。由于维生素 A 在发育和免疫系统中的视黄酸信号传导中是必需的,因此维生素 A 缺乏也会导致发展中国家儿童和孕妇的死亡率增加。黑腹果蝇是研究维生素 A 缺乏对眼睛影响的理想模型,因为维生素 A 对果蝇的发育并非必需,且慢性缺乏不会导致其死亡。此外,果蝇的遗传筛选已经确定了介导维生素 A 产生及其细胞摄取的进化保守因子。在这里,我们回顾了目前关于维生素 A 在哺乳动物和黑腹果蝇视觉系统中作用的知识。我们比较了介导膳食维生素 A 前体摄取和维生素 A 代谢的分子机制,以及维生素 A 缺乏对眼睛结构和功能的影响。