Interactions Between Amyloid-β (1-42) and Hydroxyapatite-Cholesterol Spherules Associated with Age-Related Macular Degeneration

Author(s):  
Renuka Ranjan ◽  
Arvind M. Kayastha ◽  
Neeraj Sinha
2021 ◽  
Vol 6 (1) ◽  
pp. e000774
Author(s):  
Minwei Wang ◽  
Shiqi Su ◽  
Shaoyun Jiang ◽  
Xinghuai Sun ◽  
Jiantao Wang

Age-related macular degeneration (AMD) is the most common eye disease in elderly patients, which could lead to irreversible vision loss and blindness. Increasing evidence indicates that amyloid β-peptide (Aβ) might be associated with the pathogenesis of AMD. In this review, we would like to summarise the current findings in this field. The literature search was done from 1995 to Feb, 2021 with following keywords, ‘Amyloid β-peptide and age-related macular degeneration’, ‘Inflammation and age-related macular degeneration’, ‘Angiogenesis and age-related macular degeneration’, ‘Actin cytoskeleton and amyloid β-peptide’, ‘Mitochondrial dysfunction and amyloid β-peptide’, ‘Ribosomal dysregulation and amyloid β-peptide’ using search engines Pubmed, Google Scholar and Web of Science. Aβ congregates in subretinal drusen of patients with AMD and participates in the pathogenesis of AMD through enhancing inflammatory activity, inducing mitochondrial dysfunction, altering ribosomal function, regulating the lysosomal pathway, affecting RNA splicing, modulating angiogenesis and modifying cell structure in AMD. The methods targeting Aβ are shown to inhibit inflammatory signalling pathway and restore the function of retinal pigment epithelium cells and photoreceptor cells in the subretinal region. Targeting Aβ may provide a novel therapeutic strategy for AMD.


2020 ◽  
Author(s):  
Jing Wu ◽  
Ge Gao ◽  
Fanjun Shi ◽  
Chaoyang Zhang ◽  
Hai Xie ◽  
...  

Abstract Background Age-related macular degeneration (AMD) is mainly characterized by progressive deposits of drusen and photoreceptor apoptosis. Due to amyloid β (Aβ) is the main component of drusen, there is a great possibility that Aβ-induced activated microglia leads to inflammation, and plays a critical role in the pathogenesis of AMD. However, the relationship between activated microglia-mediated neuroinflammatory cytokines and photoreceptor apoptosis still remains unclarified. Results In this study, we demonstrated that subretinal injection of Aβ1−42 induced the microglia activation and increased inflammatory cytokines, gave rise to photoreceptor apoptosis in mice. Our results were verified in vitro by co-culture of Aβ1−42 activated primary microglia and photoreceptor cell line 661W, and we also performed that p38 MAPK signaling pathway was involved in Aβ1−42 induced microglia activation and inflammatory cytokines release. Conclusions Overall, our findings indicated that activated microglia-mediated neuroinflammatory cytokines contributed to photoreceptor apoptosis under the stimulation of Aβ1−42. Moreover, this study will provide a potential preventive and therapeutic approach for AMD treatment.


2018 ◽  
Vol 2 (10) ◽  
pp. 1028-1040 ◽  
Author(s):  
Philip J. Rosenfeld ◽  
Brian Berger ◽  
Elias Reichel ◽  
Ronald P. Danis ◽  
Angie Gress ◽  
...  

2008 ◽  
Vol 181 (1) ◽  
pp. 712-720 ◽  
Author(s):  
Jiying Wang ◽  
Kyoko Ohno-Matsui ◽  
Takeshi Yoshida ◽  
Ariko Kojima ◽  
Noriaki Shimada ◽  
...  

2017 ◽  
Vol 1 (suppl_1) ◽  
pp. 427-428
Author(s):  
A.P. Bobrov ◽  
V.V. Ermilov ◽  
A. Smirnov

Biochimie ◽  
2016 ◽  
Vol 127 ◽  
pp. 70-78 ◽  
Author(s):  
Elodie Olivier ◽  
Mélody Dutot ◽  
Anne Regazzetti ◽  
Teddy Leguillier ◽  
Delphine Dargère ◽  
...  

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