Nucleoside reverse transcriptase inhibitors and Kamuvudines inhibit amyloid-β induced retinal pigmented epithelium degeneration

• Published in: Signal transduction and targeted therapy Vol. 6; no. 1; p. 149
• Main Authors: Narendran, Siddharth, Pereira, Felipe, Yerramothu, Praveen, Apicella, Ivana, Wang, Shao-Bin, Ambati, Kameshwari, Hirahara, Shuichiro, Kim, Younghee, Ambati, Meenakshi, Ambati, Vidya L, Huang, Peirong, Varshney, Akhil, Nagasaka, Yosuke, Fukuda, Shinichi, Baker, Kirstie L, Marion, Kenneth M, Deussing, Jan M, Sadda, Srinivas R, Gelfand, Bradley D, Ambati, Jayakrishna
• Format: Journal Article
• Language: English
• Published: England Nature Publishing Group 14.04.2021; Nature Publishing Group UK
• Subjects: Amyloid beta-Peptides - genetics; Amyloid beta-Peptides - metabolism; Animals; Disease Models, Animal; Humans; Macular degeneration; Macular Degeneration - drug therapy; Macular Degeneration - genetics; Macular Degeneration - metabolism; Male; Mice; Mice, Knockout; Retinal Pigment Epithelium - metabolism; Reverse Transcriptase Inhibitors - pharmacology
• ISSN: 2059-3635; 2095-9907; 2059-3635
• DOI: 10.1038/s41392-021-00537-z

Nonfibrillar amyloid-β oligomers (AβOs) are a major component of drusen, the sub-retinal pigmented epithelium (RPE) extracellular deposits characteristic of age-related macular degeneration (AMD), a common cause of global blindness. We report that AβOs induce RPE degeneration, a clinical hallmark of geographic atrophy (GA), a vision-threatening late stage of AMD that is currently untreatable. We demonstrate that AβOs induce activation of the NLRP3 inflammasome in the mouse RPE in vivo and that RPE expression of the purinergic ATP receptor P2RX7, an upstream mediator of NLRP3 inflammasome activation, is required for AβO-induced RPE degeneration. Two classes of small molecule inflammasome inhibitors-nucleoside reverse transcriptase inhibitors (NRTIs) and their antiretrovirally inert modified analog Kamuvudines-both inhibit AβOs-induced RPE degeneration. These findings crystallize the importance of P2RX7 and NLRP3 in a disease-relevant model of AMD and identify inflammasome inhibitors as potential treatments for GA.