Melatonin reprogrammes proteomic profile in light-exposed retina in vivo.
Melatonin reprogrammes proteomic profile in light-exposed retina in vivo.
复制标题
褪黑素在体内重编程暴露于光的视网膜中的蛋白质组谱。
DOI:
10.1016/j.ijbiomac.2010.04.013
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发表时间:
2010
影响因子:
8.2
通讯作者:
Jahng,WanJin
中科院分区:
文献类型:
--
作者:
Zhang,Ruonan;Hrushesky,WilliamJM;Wood,PatriciaA;Lee,SungHaeng;Hunt,RichardC;Jahng,WanJin
Melatonin, a small organic molecule synthesized by the pineal gland and the retina, has a variety of physiologic functions such as circadian clock pacemaker and antioxidant. Retinal melatonin is down-regulated by light and is barely detectable during the day. The absence of melatonin in the retina during prolonged light exposure may contribute to light-induced retinal degeneration. We sought to investigate the impact of melatonin in the light-exposed retina using proteomic approaches. We exposed mice to either light (250–300lux) for 12h followed by 12h of darkness or the same intensity of continuous light for 7 days. In half of the animals exposed to continuous light, melatonin was injected each night. Proteomic analysis of the retina from these three groups of animals showed that five proteins prominently up-regulated by constant light were down-regulated by melatonin treatment. These five proteins were identified as vimentin, serine/threonine-protein phosphatase 2A, Rab GDP dissociation inhibitor alpha, guanine nucleotide-binding protein Goalpha, and retinaldehyde-binding protein. These five proteins are known to be involved in several cellular processes that may contribute to light-induced retinal degeneration. Identification of melatonin target proteins in our study provides a basis for future studies on melatonin's potential in preventing or treating light-induced retinal degeneration.