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Eye Drop with Fas-Blocking Peptide Attenuates Age-Related Macular Degenerationopen access

Authors
Yi, YujongPyun, Seon-HongKim, Chae-YeonYun, GyeongjuKang, EunhwaHeo, SeoyounUllah, IrfanLee, Sang-Kyung
Issue Date
Mar-2024
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
age-related macular degeneration (AMD); eye drops; Fas-blocking peptide; necrosis; dry AMD; wet AMD; apoptosis; vascular endothelial growth factor (VEGF) inhibitors; anti-VEGF agents; retina
Citation
Cells, v.13, no.6, pp 1 - 19
Pages
19
Indexed
SCIE
SCOPUS
Journal Title
Cells
Volume
13
Number
6
Start Page
1
End Page
19
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/196932
DOI
10.3390/cells13060548
ISSN
2073-4409
2073-4409
Abstract
Age-related macular degeneration (AMD), characterized by macular retinal degeneration, poses a significant health concern due to the lack of effective treatments for prevalent dry AMD. The progression of AMD is closely linked to reactive oxygen species and Fas signaling, emphasizing the need for targeted interventions. In this study, we utilized a NaIO3-induced retinal degeneration mouse model to assess the efficacy of Fas-blocking peptide (FBP). Intravitreal administration of FBP successfully suppressed Fas-mediated inflammation and apoptosis, effectively arresting AMD progression in mice. We developed a 6R-conjugated FBP (6R-FBP) for eye drop administration. 6R-FBP, administered as an eye drop, reached the retinal region, attenuating degeneration by modulating the expression of inflammatory cytokines and blocking Fas-mediated apoptosis in rodent and rabbit NaIO3-induced retinal degeneration models to address practical concerns. Intravitreal FBP and 6R-FBP eye drops effectively reduced retinal degeneration and improved retinal thickness in rodent and rabbit models. This study highlights the therapeutic potential of FBP, particularly 6R-FBP as an eye drop, in inhibiting Fas-mediated cell signaling and protecting against retinal cell death and inflammation in dry AMD. Future investigations should explore the translational prospects of this approach in primates with eye structures comparable to those of humans.
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