Lou Marjorie F
School of Veterinary Medicine and Biomedical Sciences, Redox Biology Center, University of Nebraska-Lincoln, Lincoln, NE 68583, USA.
Department of Ophthalmology, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Antioxidants (Basel). 2022 Oct 1;11(10):1973. doi: 10.3390/antiox11101973.
The ocular lens has a very high content of the antioxidant glutathione (GSH) and the enzymes that can recycle its oxidized form, glutathione disulfide (GSSG), for further use. It can be synthesized in the lens and, in part, transported from the neighboring anterior aqueous humor and posterior vitreous body. GSH is known to protect the thiols of the structural lens crystallin proteins from oxidation by reactive oxygen species (ROS) so the lens can maintain its transparency for proper visual function. Age-related lens opacity or senile cataract is the major visual impairment in the general population, and its cause is closely associated with aging and a constant exposure to environmental oxidative stress, such as ultraviolet light and the metabolic end product, HO. The mechanism for senile cataractogenesis has been hypothesized as the results of oxidation-induced protein-thiol mixed disulfide formation, such as protein-S-S-glutathione and protein-S-S-cysteine mixed disulfides, which if not reduced in time, can change the protein conformation to allow cascading modifications of various kinds leading to protein-protein aggregation and insolubilization. The consequence of such changes in lens structural proteins is lens opacity. Besides GSH, the lens has several antioxidation defense enzymes that can repair oxidation damage. One of the specific redox regulating enzymes that has been recently identified is thioltransferase (glutaredoxin 1), which works in concert with GSH, to reduce the oxidative stress as well as to regulate thiol/disulfide redox balance by preventing protein-thiol mixed disulfide accumulation in the lens. This oxidation-resistant and inducible enzyme has multiple physiological functions. In addition to protecting structural proteins and metabolic enzymes, it is able to regulate the redox signaling of the cells during growth factor-stimulated cell proliferation and other cellular functions. This review article focuses on describing the redox regulating functions of GSH and the thioltransferase enzyme in the ocular lens.
晶状体含有非常高含量的抗氧化剂谷胱甘肽(GSH)以及能够将其氧化形式二硫化谷胱甘肽(GSSG)循环再利用以供进一步使用的酶。它可以在晶状体中合成,部分则从相邻的眼前房和玻璃体运输而来。众所周知,GSH可保护晶状体结构蛋白的硫醇免受活性氧(ROS)的氧化,从而使晶状体能够保持其透明度以实现正常视觉功能。年龄相关性晶状体混浊或老年性白内障是普通人群中的主要视力障碍,其病因与衰老以及持续暴露于环境氧化应激(如紫外线和代谢终产物HO)密切相关。老年性白内障形成的机制被假设为氧化诱导的蛋白质 - 硫醇混合二硫化物形成的结果,例如蛋白质 - S - S - 谷胱甘肽和蛋白质 - S - S - 半胱氨酸混合二硫化物,如果不能及时还原,会改变蛋白质构象,引发各种级联修饰,导致蛋白质 - 蛋白质聚集和不溶性。晶状体结构蛋白的这种变化的结果就是晶状体混浊。除了GSH,晶状体还有几种抗氧化防御酶,可以修复氧化损伤。最近发现的一种特定的氧化还原调节酶是硫醇转移酶(谷氧还蛋白1),它与GSH协同作用,通过防止蛋白质 - 硫醇混合二硫化物在晶状体中积累来降低氧化应激并调节硫醇/二硫化物氧化还原平衡。这种抗氧化且可诱导的酶具有多种生理功能。除了保护结构蛋白和代谢酶外,它还能够在生长因子刺激的细胞增殖和其他细胞功能过程中调节细胞的氧化还原信号。这篇综述文章重点描述了GSH和硫醇转移酶在晶状体中的氧化还原调节功能。