Use este identificador para citar o ir al link de este elemento: http://hdl.handle.net/1843/82394
Tipo: Artigo de Periódico
Título: Neutrophil extracellular traps mediate bone erosion in rheumatoid arthritis by enhancing RANKL-induced osteoclastogenesis
Autor(es): Ayda Henriques Schneider
Renê Donizeti Ribeiro de Oliveira
Thiago Mattar Cunha
José Carlos Alves-Filho
Paulo Louzada-Júnior
Tarcília Aparecida da Silva
Sandra Yasuyo Fukada Alves
Fernando de Queiroz Cunha
Thaise Mayumi Taira
Gabriel Azevedo Públio
Douglas da Silva Prado
Paula Barbim Donate Yabuta
Jéssica Cristina Dos Santos
Caio Cavalcante Machado
Flávio Falcão Lima de Souza
Lucas Gabriel Rodrigues Venturini
Resumen: Background and Purpose:Rheumatoid arthritis (RA) is a chronic autoimmune disease that can cause bone erosion due to increased osteoclastogenesis. Neutrophils involvement in osteoclastogenesis remains uncertain. Given that neutrophil extracellular traps (NETs) can act as inflammatory mediators in rheumatoid arthritis, we investigated the role of NETs in stimulating bone loss by potentiating osteoclastogenesis during arthritis. Experimental Approach: The level of NETs in synovial fluid from arthritis patients was assessed. Bone loss was evaluated by histology and micro-CT in antigen-induced arthritis (AIA)-induced WT mice treated with DNase or in Padi4-deficient mice (Padi4flox/flox LysMCRE). The size and function of osteoclasts and the levels of RANKL and osteoprotegerin (OPG) released by osteoblasts that were incubated with NETs were measured. The expression of osteoclastogenic marker genes and protein levels were evaluated by qPCR and western blotting. To assess the participation of TLR4 and TLR9 in osteoclastogenesis, cells from Tlr4−/− and Tlr9−/− mice were cultured with NETs. Key Results: Rheumatoid arthritis patients had higher levels of NETs in synovial fluid than osteoarthritis patients, which correlated with increased levels of RANKL/OPG. Moreover, patients with bone erosion had higher levels of NETs. Inhibiting NETs with DNase or Padi4 deletion alleviated bone loss in arthritic mice. Consistently, NETs enhanced RANKL-induced osteoclastogenesis that was dependent on TLR4 and TLR9 and increased osteoclast resorptive functions in vitro. In addition, NETs stimulated the release of RANKL and inhibited osteoprotegerin in osteoblasts, favouring osteoclastogenesis. Conclusions and Implications: Inhibiting NETs could be an alternative strategy to reduce bone erosion in arthritis patients.
Asunto: Osteogenesis
Extracellular traps
Osteoclasts
Arthritis, rheumatoid
RANK Ligand
Protein-arginine deiminase type 4
Deoxyribonucleases
Osteoprotegerin
Toll-like receptor 4
Toll-like receptor 9
Bone resorption
Osteoblasts
Idioma: eng
País: Brasil
Editor: Universidade Federal de Minas Gerais
Sigla da Institución: UFMG
Departamento: FAO - DEPARTAMENTO DE CLÍNICA
Tipo de acceso: Acesso Restrito
Identificador DOI: https://doi.org/10.1111/bph.16227
URI: http://hdl.handle.net/1843/82394
Fecha del documento: feb-2024
metadata.dc.url.externa: https://bpspubs.onlinelibrary.wiley.com/doi/10.1111/bph.16227
metadata.dc.relation.ispartof: British Journal of Pharmacology
Aparece en las colecciones:Artigo de Periódico

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