دورية أكاديمية

TLR dependent XBP-1 activation induces an autocrine loop in rheumatoid arthritis synoviocytes

التفاصيل البيبلوغرافية
العنوان: TLR dependent XBP-1 activation induces an autocrine loop in rheumatoid arthritis synoviocytes
المؤلفون: Savic, Sinisa, Ouboussad, Lylia, Dickie, Laura J, Geiler, Janina, Wong, Chi, Doody, Gina M, Churchman, Sarah M, Ponchel, Frederique, Emery, Paul, Cook, Graham P, Buch, Maya H, Tooze, Reuben M, McDermott, Michael F
المصدر: Savic , S , Ouboussad , L , Dickie , L J , Geiler , J , Wong , C , Doody , G M , Churchman , S M , Ponchel , F , Emery , P , Cook , G P , Buch , M H , Tooze , R M & McDermott , M F 2014 , ' TLR dependent XBP-1 activation induces an autocrine loop in rheumatoid arthritis synoviocytes ' , Journal of Autoimmunity , vol. 50 , pp. 59-66 . https://doi.org/10.1016/j.jaut.2013.11.002Test
سنة النشر: 2014
المجموعة: The University of Manchester: Research Explorer - Publications
مصطلحات موضوعية: Arthritis, Rheumatoid/genetics, Autocrine Communication, Case-Control Studies, DNA-Binding Proteins/agonists, Endoplasmic Reticulum/drug effects, Endoplasmic Reticulum Stress/drug effects, Fibroblasts/drug effects, Gene Expression Regulation, Humans, Interleukin-6/genetics, Lipopolysaccharides/pharmacology, Primary Cell Culture, Regulatory Factor X Transcription Factors, Signal Transduction, Synovial Membrane/drug effects, Toll-Like Receptor 2/agonists, Toll-Like Receptor 4/agonists, Transcription Factors/agonists, Tumor Necrosis Factor-alpha/genetics, X-Box Binding Protein 1
الوصف: X-box binding protein 1 (XBP1) is a central regulator of the endoplasmic reticulum (ER) stress response. It is induced via activation of the IRE1 stress sensor as part of the unfolded protein response (UPR) and has been implicated in several diseases processes. XBP1 can also be activated in direct response to Toll-like receptor (TLR) ligation independently of the UPR but the pathogenic significance of this mode of XBP1 activation is not well understood. Here we show that TLR-dependent XBP1 activation is operative in the synovial fibroblasts (SF) of patients with active rheumatoid arthritis (RA). We investigated the expression of ER stress response genes in patients with active RA and also in patients in remission. The active (spliced) form of (s)XBP1 was significantly overexpressed in the active RA group compared to healthy controls and patients in remission. Paradoxically, expression of nine other ER stress response genes was reduced in active RA compared to patients in remission, suggestive of a UPR-independent process. However, sXBP1 was induced in SF by TLR4 and TLR2 stimulation, resulting in sXBP1-dependent interleukin-6 and tumour necrosis factor (TNF) production. We also show that TNF itself induces sXBP1 in SF, thus generating a potential feedback loop for sustained SF activation. These data confirm the first link between TLR-dependent XBP1 activation and human inflammatory disease. sXBP1 appears to play a central role in this process by providing a convergence point for two different stimuli to maintain activation of SF.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1016/j.jaut.2013.11.002
الإتاحة: https://doi.org/10.1016/j.jaut.2013.11.002Test
https://research.manchester.ac.uk/en/publications/e453d177-ca2c-4ac0-ae13-ff429cd281d0Test
حقوق: info:eu-repo/semantics/restrictedAccess
رقم الانضمام: edsbas.E87D21A1
قاعدة البيانات: BASE