Lou M F
Center for Biotechnology, Department of Veterinary and Biomedical Sciences, University of Nebraska, Lincoln 68583-0905, USA.
J Ocul Pharmacol Ther. 2000 Apr;16(2):137-48. doi: 10.1089/jop.2000.16.137.
The high content of glutathione (GSH) in the lens is believed to protect the thiols in structural proteins and enzymes for proper biological functions. The lens has both biosynthetic and regenerating systems for GSH to maintain its large pool size (4-6 mM). However, we have observed that, in aging lenses or lenses under oxidative stress, the size of GSH pool is diminished; and some protein thiols are being S-thiolated by oxidized nonprotein thiols to form protein-thiol mixed disulfides, either as protein-S-S-glutathione (PSSG) or protein-S-S-cysteine (PSSC). We have shown in an H2O2-induced cataract model that PSSG formation precedes a cascade of events starting with protein disulfide crosslinks, protein solubility loss, and eventual lens opacification. Recently, we discovered that this early oxidative damage in protein thiols could be spontaneously reversed in H2O2 pretreated lenses if the oxidant was removed in time. This dethiolation process is likely mediated through a redox regulating enzyme, thioltransferase (TTase), which has been discovered recently in the lens. To understand if the role of oxidative defense and repair is the physiological function of TTase in the lens, we cloned the TTase gene and purified the recombinant human lens TTase. Although TTase required GSH for its activity, TTase was far more efficient in dethiolating lens proteins than GSH alone. It favored PSSG over PSSC and dethiolated gamma-crystallin-S-S-G better than the alpha-crystallin counterparts. Furthermore, TTase showed a remarkable resistance to oxidation (H2O2) in cultured rabbit lens epithelial cells when GSH peroxidase, GSH reductase, and glyceraldehyde-3-phosphate dehydrogenase were severely inactivated. We further showed that activity loss in those SH sensitive enzymes could be attributed to S-thiolation, but reactivation via dethiolation could be attributed to TTase. We conclude that TTase can regulate and repair the thiols in lens proteins and enzymes through its dethiolase activity, thus contributing to the maintenance of the function of the lens.
晶状体中高含量的谷胱甘肽(GSH)被认为可保护结构蛋白和酶中的硫醇,以实现正常的生物学功能。晶状体具有GSH的生物合成和再生系统,以维持其大量储备(4 - 6 mM)。然而,我们观察到,在老化晶状体或处于氧化应激的晶状体中,GSH储备量会减少;并且一些蛋白质硫醇会被氧化的非蛋白质硫醇进行S-硫醇化,形成蛋白质-硫醇混合二硫键,即蛋白质-S-S-谷胱甘肽(PSSG)或蛋白质-S-S-半胱氨酸(PSSC)。我们在过氧化氢诱导的白内障模型中表明,PSSG的形成先于一系列事件,这些事件始于蛋白质二硫键交联、蛋白质溶解度丧失以及最终的晶状体混浊。最近,我们发现,如果及时去除氧化剂,在过氧化氢预处理的晶状体中,蛋白质硫醇的这种早期氧化损伤可以自发逆转。这种脱硫醇过程可能是通过一种氧化还原调节酶——硫醇转移酶(TTase)介导的,该酶最近在晶状体中被发现。为了解氧化防御和修复作用是否是TTase在晶状体中的生理功能,我们克隆了TTase基因并纯化了重组人晶状体TTase。尽管TTase的活性需要GSH,但TTase在使晶状体蛋白脱硫醇方面比单独的GSH效率高得多。它更倾向于PSSG而非PSSC,并且比α-晶状体蛋白更有效地使γ-晶状体蛋白-S-S-G脱硫醇。此外,当谷胱甘肽过氧化物酶、谷胱甘肽还原酶和甘油醛-3-磷酸脱氢酶严重失活时,TTase在培养的兔晶状体上皮细胞中表现出对氧化(过氧化氢)的显著抗性。我们进一步表明,那些对SH敏感的酶的活性丧失可归因于S-硫醇化,但通过脱硫醇实现的再激活可归因于TTase。我们得出结论,TTase可以通过其脱硫醇酶活性调节和修复晶状体蛋白和酶中的硫醇,从而有助于维持晶状体的功能。