Role of transient receptor potential vanilloid 4 in rat joint inflammation


Autoria(s): Denadai-Souza, Alexandre; Martin, Laurence; Paula, Marco Aurélio Vieira de; de Avellar, Maria C. Werneck; Muscara, Marcelo Nicolas; Vergnolle, Nathalie; Cenac, Nicolas
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

23/10/2013

23/10/2013

2012

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

http://dx.doi.org/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