Regulation of Fn14 Receptor and NF-kappa B Underlies Inflammation in Meniere's Disease

• Tipo: Artigo em Revista Científica Internacional
• Data: 2017

Autores

Frejo, L (Autor) Outra; Requena, T (Autor) Outra; Okawa, S (Autor) Outra; Gallego Martinez, A (Autor) Outra; Martinez Bueno, M (Autor) Outra; Aran, I (Autor) Outra; Batuecas Caletrio, A (Autor) Outra; Benitez Rosario, J (Autor) Outra; Espinosa Sanchez, JM (Autor) Outra; Fraile Rodrigo, JJ (Autor) Outra; Garcia Arumi, AM (Autor) Outra; Gonzalez Aguado, R (Autor) Outra; Marques, P (Autor) FMUP; Martin Sanz, E (Autor) Outra; Perez Fernandez, N (Autor) Outra; Perez Vazquez, P (Autor) Outra; Perez Garrigues, H (Autor) Outra; Santos Perez, S (Autor) Outra; Soto Varela, A (Autor) Outra; Tapia, MC (Autor) Outra; Trinidad Ruiz, G (Autor) Outra; del Sol, A (Autor) Outra; Riquelme, MEA (Autor) Outra; Lopez Escamez, JA (Autor) Outra

Revista

Título: Frontiers In Immunology

Vol. 8

ISSN: 1664-3224

Editora: Frontiers Media

Indexação

ISI Web of Knowledge - 42 Citações

Scopus - 47 Citações

Outras Informações

ID Authenticus: P-00N-BZX

DOI: 10.3389/fimmu.2017.01739

Abstract (EN): Meniere's disease (MD) is a rare disorder characterized by episodic vertigo, sensorineural hearing loss, tinnitus, and aural fullness. It is associated with a fluid imbalance between the secretion of endolymph in the cochlear duct and its reabsorption into the subarachnoid space, leading to an accumulation of endolymph in the inner ear. Epidemiological evidence, including familial aggregation, indicates a genetic contribution and a consistent association with autoimmune diseases (AD). We conducted a case-control study in two phases using an immune genotyping array in a total of 420 patients with bilateral MD and 1,630 controls. We have identified the first locus, at 6p21.33, suggesting an association with bilateral MD [meta-analysis leading signal rs4947296, OR = 2.089 (1.661-2.627); p = 1.39 x 10(-09)]. Gene expression profiles of homozygous genotype-selected peripheral blood mononuclear cells (PBMCs) demonstrated that this region is a trans-expression quantitative trait locus (eQTL) in PBMCs. Signaling analysis predicted several tumor necrosis factor-related pathways, the TWEAK/Fn14 pathway being the top candidate (p = 2.42 x 10(-11)). This pathway is involved in the modulation of inflammation in several human AD, including multiple sclerosis, systemic lupus erythematosus, or rheumatoid arthritis. In vitro studies with genotype-selected lymphoblastoid cells from patients with MD suggest that this trans-eQTL may regulate cellular proliferation in lymphoid cells through the TWEAK/Fn14 pathway by increasing the translation of NF-kappa B. Taken together; these findings suggest that the carriers of the risk genotype may develop an NF-kappa B-mediated inflammatory response in MD.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 15