Lysophosphatidic acid receptor 1 suppression sensitizes rheuamatoid fibroblast-like synoviocytes to tumor necrosis factor-induced apoptosis

[EN] Objective. To investigate the role of lysophosphatidic acid (LPA) receptors in the proliferation and apoptosis of fibroblast-like synoviocytes (FLS) from patients with rheumatoid arthritis (RA). Methods. Expression of LPA receptors 1–3 was analyzed by real-time polymerase chain reaction (PCR)....

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Detalhes bibliográficos
Autores: Orosa, Beatriz, González Martínez-Pedrayo, Antonio, Mera Varela, Antonio, Gómez-Reino Carnota, Juan Jesús, Conde Muro, Carmen
Formato: artículo
Fecha de publicación:2012
País:España
Recursos:Servizo Galego de Saúde (SERGAS)
Repositorio:RUNA. Repositorio da Consellería de Sanidade e Sergas
OAI Identifier:oai:runa.sergas.gal:20.500.11940/17721
Acesso em linha:https://pubmed.ncbi.nlm.nih.gov/22354754/
http://hdl.handle.net/20.500.11940/17721
Access Level:acceso abierto
Palavra-chave:Apoptosis
Synoviocytes
Arthritis, Rheumatoid
RNA, Messenger
TNF Receptor-Associated Death Domain Protein
Blotting, Western
Receptors, Lysophosphatidic Acid
apoptosis
proteína del dominio de muerte asociada a receptores TNF
inmunotransferencia Western
artritis reumatoide
receptores de ácidos lisofosfatídicos
ARN mensajero
CHUS
Descrição
Resumo:[EN] Objective. To investigate the role of lysophosphatidic acid (LPA) receptors in the proliferation and apoptosis of fibroblast-like synoviocytes (FLS) from patients with rheumatoid arthritis (RA). Methods. Expression of LPA receptors 1–3 was analyzed by real-time polymerase chain reaction (PCR). LPAR1 and LPAR2 were suppressed in RA FLS by small interfering RNA (siRNA) transfection. Proliferation of RA FLS after tumor necrosis factor (TNF) and LPA stimulation was determined with a luminescent cell viability assay. Apoptosis was analyzed by quantification of nucleosome release and measurement of activated caspase 3/7. Genes involved in the apoptotic response were identified with a human apoptosis PCR array and validated with Western blot assays. The requirement of these genes for apoptosis sensitization was assessed by siRNA transfection. Secretion of mediators of inflammation was analyzed by enzyme-linked immunosorbent assay. Results. Only LPAR1 and LPAR2 were expressed by RA FLS, and their levels were higher than those in osteoarthritis (OA) FLS. Suppression of LPAR1 abrogated TNF-induced proliferation and sensitized the RA FLS, but not the OA FLS, to TNF-induced apoptosis. These changes occurred despite an increased early inflammatory response to TNF. Sensitization to apoptosis was associated with changes in expression of multiple apoptosis-related genes. Three of the up-regulated proapoptotic genes were further studied to confirm their involvement. In contrast, suppression of LPAR2 showed no effect in any of these analyses. Conclusion. LPA1 is an important receptor in RA FLS. Its suppression is accompanied by a global increase in the response to TNF that is ultimately dominated by sensitization to apoptosis.