Role of transient receptor potential vanilloid 4 in rat joint inflammation
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
23/10/2013
23/10/2013
2012
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Resumo |
Objective To determine whether activation of transient receptor potential vanilloid 4 (TRPV-4) induces inflammation in the rat temporomandibular joint (TMJ), and to assess the effects of TRPV-4 agonists and proinflammatory mediators, such as a protease-activated receptor 2 (PAR-2) agonist, on TRPV-4 responses. Methods Four hours after intraarticular injection of carrageenan into the rat joints, expression of TRPV-4 and PAR-2 in trigeminal ganglion (TG) neurons and in the TMJs were evaluated by real-time reverse transcriptionpolymerase chain reaction and immunofluorescence, followed by confocal microscopy. The functionality of TRPV-4 and its sensitization by a PAR-2activating peptide (PAR-2AP) were analyzed by measuring the intracellular Ca2+ concentration in TMJ fibroblast-like synovial cells or TG neurons. Plasma extravasation, myeloperoxidase activity, and the head-withdrawal threshold (index of mechanical allodynia) were evaluated after intraarticular injection of selective TRPV-4 agonists, either injected alone or coinjected with PAR-2AP. Results In the rat TMJs, TRPV-4 and PAR-2 expression levels were up-regulated after the induction of inflammation. Two TRPV-4 agonists specifically activated calcium influx in TMJ fibroblast-like synovial cells or TG neurons. In vivo, the agonists triggered dose-dependent increases in plasma extravasation, myeloperoxidase activity, and mechanical allodynia. In synovial cells or TG neurons, pretreatment with PAR-2AP potentiated a TRPV-4 agonistinduced increase in [Ca2+]i. In addition, TRPV-4 agonistinduced inflammation was potentiated by PAR-2AP in vivo. Conclusion In this rat model, TRPV-4 is expressed and functional in TG neurons and synovial cells, and activation of TRPV-4 in vivo causes inflammation in the TMJ. Proinflammatory mediators, such as PAR-2 agonists, sensitize the activity of TRPV-4. These results identify TRPV-4 as an important signal of inflammation in the joint. INSERMAvenir INSERM-Avenir BettencourtSchueller Foundation Bettencourt-Schueller Foundation Foundation for Medical Research Foundation for Medical Research Agence Nationale de la Recherche Agence Nationale de la Recherche Canadian Institute of Health Research Canadian Institute of Health Research Coordination for the Improvement of Higher Education Personnel (CAPES) Foundation Foundation for the Coordination of Improvement of Higher Education Personnel (CAPES) CNPq CNPq Sao Paulo Research Foundation (FAPESP) [2009/12375-3] Sao Paulo Research Foundation (FAPESP) |
Identificador |
ARTHRITIS AND RHEUMATISM, HOBOKEN, v. 64, n. 6, supl. 1, Part 2, pp. 1848-1858, JUN, 2012 0004-3591 http://www.producao.usp.br/handle/BDPI/35684 10.1002/art.34345 |
Idioma(s) |
eng |
Publicador |
WILEY-BLACKWELL HOBOKEN |
Relação |
ARTHRITIS AND RHEUMATISM |
Direitos |
closedAccess Copyright WILEY-BLACKWELL |
Palavras-Chave | #PROTEINASE-ACTIVATED RECEPTOR-2 #SENSITIVE ION-CHANNEL #CATION CHANNEL #VISCERAL HYPERSENSITIVITY #TEMPOROMANDIBULAR-JOINT #ARTICULAR CHONDROCYTES #RHEUMATOID-ARTHRITIS #TRPV4 CHANNELS #EXPRESSION #OSTEOARTHRITIS #RHEUMATOLOGY |
Tipo |
article original article publishedVersion |