دورية أكاديمية

TRPV1 Gates Tissue Access and Sustains Pathogenicity in Autoimmune Encephalitis

التفاصيل البيبلوغرافية
العنوان: TRPV1 Gates Tissue Access and Sustains Pathogenicity in Autoimmune Encephalitis
المؤلفون: Geoffrey Paltser, Xue Jun Liu, Jason Yantha, Shawn Winer, Hubert Tsui, Ping Wu, Yuko Maezawa, Lindsay S. Cahill, Christine L. Laliberté, Sreeram V. Ramagopalan, Gabriele C. DeLuca, A. Dessa Sadovnick, Igor Astsaturov, George C. Ebers, R. Mark Henkelman, Michael W. Salter, H.-Michael Dosch
المصدر: Molecular Medicine, Vol 19, Iss 1, Pp 149-159 (2013)
بيانات النشر: BMC, 2013.
سنة النشر: 2013
المجموعة: LCC:Therapeutics. Pharmacology
LCC:Biochemistry
مصطلحات موضوعية: Transient Receptor Potential Vanilloid (TRPV1), Experimental Autoimmune Encephalomyelitis, TRPV1 Activation, Blood-spinal Cord Barrier (BSCB), TRPV1 Expression, Therapeutics. Pharmacology, RM1-950, Biochemistry, QD415-436
الوصف: Abstract Multiple sclerosis (MS) is a chronic progressive, demyelinating condition whose therapeutic needs are unmet, and whose pathoetiology is elusive. We report that transient receptor potential vanilloid-1 (TRPV1) expressed in a major sensory neuron subset, controls severity and progression of experimental autoimmune encephalomyelitis (EAE) in mice and likely in primary progressive MS. TRPV1−/− B6 congenics are protected from EAE. Increased survival reflects reduced central nervous systems (CNS) infiltration, despite indistinguishable T cell autoreactivity and pathogenicity in the periphery of TRPV1-sufficient and -deficient mice. The TRPV1+ neurovascular complex defining the blood-CNS barriers promoted invasion of pathogenic lymphocytes without the contribution of TRPV1-dependent neuropeptides such as substance P In MS patients, we found a selective risk-association of the missense rs877610 TRPV1 single nucleotide polymorphism (SNP) in primary progressive disease. Our findings indicate that TRPV1 is a critical disease modifier in EAE, and we identify a predictor of severe disease course and a novel target for MS therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1076-1551
1528-3658
العلاقة: https://doaj.org/toc/1076-1551Test; https://doaj.org/toc/1528-3658Test
DOI: 10.2119/molmed.2012.00329
الوصول الحر: https://doaj.org/article/e5890ad622bf4df7ba2d1d634ebcb2deTest
رقم الانضمام: edsdoj.5890ad622bf4df7ba2d1d634ebcb2de
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10761551
15283658
DOI:10.2119/molmed.2012.00329