The lens cells and their protein constituents have to remain functional for a lifetime to preserve the transparent function of the lens. Damage to lens proteins results in protein aggregation and cataract. Efficient removal and/or repair of damaged lens proteins is essential to prevent protein aggregation and cataract formation. The damage is normally prevented and repaired through the action of multiple anti-oxidant, chaperone and protein repair enzymes. Damaged proteins that are not repairable must be degraded to prevent aggregation and precipitation, a major mechanism of cataractogenesis. Our previous work demonstrated that a proteolytic system named the ubiquitinproteasome pathway plays an important role in selective removal of damaged or abnormal proteins from lens cells. To directly test the role of the ubiquitin-proteasome pathway in quality control of lens proteins, we will test whether impairment of the ubiquitin-proteasome pathway increases levels of various forms of damaged proteins in the lens and reduces lens transparency. The proposed work will increase our knowledge of how the lens maintains its transparent function and will potentially identify targets of pharmaceutical interventions for prevention or treatment of age-related cataract.

Public Health Relevance

Cataract is the most common age-related eye diseases. Currently surgery is only effective methods to restore the vision loss caused by cataract. Elucidating the molecular mechanisms of cataract formation will help to develop safer, cheaper and more effective methods to prevent or treat agerelated cataract. During the last grant period we demonstrate that the ubiquitin-proteasome pathway is an important protein quality control mechanism in the lens. The selective degradation of various forms of damaged proteins by this pathway is important for preventing the accumulation and precipitation of damaged proteins in the lens. This proposed project will continue our work to demonstrate the critical role of the ubiquitin-proteasome pathway in maintaining lens transparency. Results from this project will help us to design new strategies for prevention and treatment of cataract.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
2R01EY011717-11A2
Application #
7784700
Study Section
Anterior Eye Disease Study Section (AED)
Program Officer
Araj, Houmam H
Project Start
1998-01-01
Project End
2012-01-31
Budget Start
2010-02-01
Budget End
2012-01-31
Support Year
11
Fiscal Year
2010
Total Cost
$390,260
Indirect Cost
Name
Tufts University
Department
Nutrition
Type
Organized Research Units
DUNS #
039318308
City
Boston
State
MA
Country
United States
Zip Code
02111
Lyu, Lei; Whitcomb, Elizabeth A; Jiang, Shuhong et al. (2016) Unfolded-protein response-associated stabilization of p27(Cdkn1b) interferes with lens fiber cell denucleation, leading to cataract. FASEB J 30:1087-95
Liu, Zhenzhen; Qin, Tingyu; Zhou, Jilin et al. (2014) Impairment of the ubiquitin-proteasome pathway in RPE alters the expression of inflammation related genes. Adv Exp Med Biol 801:237-50
Bian, Qingning; Gao, Shasha; Zhou, Jilin et al. (2012) Lutein and zeaxanthin supplementation reduces photooxidative damage and modulates the expression of inflammation-related genes in retinal pigment epithelial cells. Free Radic Biol Med 53:1298-307
Liu, Zhenzhen; Taylor, Allen; Liu, Yizhi et al. (2012) Enhancement of ubiquitin conjugation activity reduces intracellular aggregation of V76D mutant ?D-crystallin. Invest Ophthalmol Vis Sci 53:6655-65
Shang, Fu; Taylor, Allen (2012) Roles for the ubiquitin-proteasome pathway in protein quality control and signaling in the retina: implications in the pathogenesis of age-related macular degeneration. Mol Aspects Med 33:446-66
Shang, Fu; Taylor, Allen (2012) Role of the ubiquitin-proteasome in protein quality control and signaling: implication in the pathogenesis of eye diseases. Prog Mol Biol Transl Sci 109:347-96
Wu, Mingxing; Zhang, Xinyu; Bian, Qingning et al. (2012) Oligomerization with wt ýýA- and ýýB-crystallins reduces proteasome-mediated degradation of C-terminally truncated ýýA-crystallin. Invest Ophthalmol Vis Sci 53:2541-50
Bian, Qingning; Qin, Tingyu; Ren, Zhihong et al. (2012) Lutein or zeaxanthin supplementation suppresses inflammatory responses in retinal pigment epithelial cells and macrophages. Adv Exp Med Biol 723:43-50
Shang, Fu; Taylor, Allen (2011) Ubiquitin-proteasome pathway and cellular responses to oxidative stress. Free Radic Biol Med 51:5-16
Gao, Shasha; Qin, Tingyu; Liu, Zhenzhen et al. (2011) Lutein and zeaxanthin supplementation reduces H2O2-induced oxidative damage in human lens epithelial cells. Mol Vis 17:3180-90

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