Regulation of Fn14 Receptor and NF-κB Underlies Inflammation in Meniere’s Disease

Lidia Frejo(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), Teresa Requena(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), Satoshi Okawa(University of Luxembourg), Alvaro Gallego‐Martinez(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), Manuel Martínez‐Bueno(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), Ismael Arán(Complejo Hospitalario de Pontevedra), Ángel Batuecas Caletrío(Instituto de Investigación Biomédica de Salamanca), Jesús Benitez-Rosario(Hospital Universitario de Gran Canaria Doctor Negrín), Juan Manuel Espinosa-Sánchez(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), Jesús Fraile-Rodrigo(Hospital Universitario Miguel Servet), Ana María García-Arumí(Vall d'Hebron Hospital Universitari), Rocío González‐Aguado(Marqués de Valdecilla University Hospital), Pedro Marques(Universidade do Porto), Eduardo Martín-Sanz(Hospital Universitario de Getafe), Nicolás Pérez‐Fernández(Clinica Universidad de Navarra), Paz Pérez-Vázquez(Hospital Universitario De Cabueñes), Herminio Pérez-Garrigues, Sofía Santos-Pérez(Complejo Hospitalario Universitario de Santiago), Andrés Soto-Varela(Complexo Hospitalario Universitario A Coruña), Maria C. Tapia, Gabriel Ruiz(Centro de Implantología Cirugía Oral y Maxilofacial), Antonio del Sol(University of Luxembourg), Marta E. Alarcón‐Riquelme(Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research), José A. López‐Escámez(Hospital Universitario Virgen de las Nieves)
Frontiers in Immunology
December 13, 2017
Cited by 67Open Access
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Abstract

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. We conducted a case-control study in two phases using an immune genotyping array in a total of 420 patients with bilateral MD and 1630 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= 1.39x 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 TNF-related pathways, being the TWEAK/Fn14 pathway the top candidate (p= 2.42 x 10-11). This pathway is involved in the modulation of inflammation in several human autoimmune diseases, 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-κB. Taken together; these findings suggest that the carriers of the risk genotype may develop an NF-κB-mediated inflammatory response in MD.


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