Nature communications · 2017
DEK-targeting DNA aptamers as therapeutics for inflammatory arthritis.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Mor-Vaknin Nirit, Saha Anjan, Legendre Maureen, Carmona-Rivera Carmelo, Amin M Asif, Rabquer Bradley J, Gonzales-Hernandez Marta J, Jorns Julie, Mohan Smriti, Yalavarthi Srilakshmi, Pai Dave A, Angevine Kristine, Almburg Shelley J, Knight Jason S, Adams Barbara S, Koch Alisa E, Fox David A, Engelke David R, Kaplan Mariana J, Markovitz David M
Аннотация
Novel therapeutics are required for improving the management of chronic inflammatory diseases. Aptamers are single-stranded RNA or DNA molecules that have recently shown utility in a clinical setting, as they can specifically neutralize biomedically relevant proteins, particularly cell surface and extracellular proteins. The nuclear chromatin protein DEK is a secreted chemoattractant that is abundant in the synovia of patients with juvenile idiopathic arthritis (JIA). Here, we show that DEK is crucial to the development of arthritis in mouse models, thus making it an appropriate target for aptamer-based therapy. Genetic depletion of DEK or treatment with DEK-targeted aptamers significantly reduces joint inflammation in vivo and greatly impairs the ability of neutrophils to form neutrophil extracellular traps (NETs). DEK is detected in spontaneously forming NETs from JIA patient synovial neutrophils, and DEK-targeted aptamers reduce NET formation. DEK is thus key to joint inflammation, and anti-DEK aptamers hold promise for the treatment of JIA and other types of arthritis.
Предметные рубрики MeSH
AdultAnimalsAptamers, NucleotideArthritis, JuvenileChemotactic FactorsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDisease Models, AnimalExtracellular TrapsFemaleHealthy VolunteersHumansMaleMiceMice, Inbred C57BLMice, KnockoutNeutrophilsOncogene ProteinsPoly-ADP-Ribose Binding ProteinsPrimary Cell CultureSynovial FluidZymosan