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Biol. Res ; 48: 1-8, 2015. ilus, graf, tab
Artigo em Inglês | LILACS | ID: biblio-950828

RESUMO

BACKGROUND: Osteoarthritis (OA) is a common arthritic disease and multifactorial whole-joint disease. Interactions of chemokines and OA is inadequately documented. RESULTS: In vivo and in vitro studies were conducted to investigate monocyte chemoattractant protein 1 (MCP-1) and receptor chemokine (C-C motif) receptor 2 (CCR2) in chondrocyte degradation and cartilage degeneration. Chondrocytes from 16 OA patients and 6 normal controls were involved in this study. After stimulation of MCP-1, the expression of MCP-1 and CCR2 increased significantly (P < 0.001) and the expression of MMP-13 also increased (P < 0.05). MCP-1 stimulation also induced (or enhanced) the apoptosis of OA chondrocytes (P < 0.05). Additionally, the degradation of cartilage matrix markers (metalloproteinase 3 and 13, MMP3 and MMP13) in the culture medium of normal chondrocytes was also assessed. Furthermore, intra-articular injection of MCP-1 in mouse knees induced cartilage degradation and the CCR2 antagonist did not impede cartilage destroy in rats knees of monosodium iodoacetate (MIA) model. CONCLUSIONS: The results of this study demonstrate that the MCP-1-CCR2 ligand-receptor axis plays a special role in the initiation and progression of OA pathology. Patients with ambiguous etiology can gain some insight from the MCP-1-CCR2 ligand-receptor axis.


Assuntos
Humanos , Animais , Masculino , Feminino , Adolescente , Pessoa de Meia-Idade , Idoso , Camundongos , Ratos , Adulto Jovem , Quimiocina CCL2/metabolismo , Condrócitos/metabolismo , Osteoartrite do Joelho/fisiopatologia , Receptores CCR2/metabolismo , Membrana Sinovial/citologia , Técnicas In Vitro , Ensaio de Imunoadsorção Enzimática , Ratos Sprague-Dawley , Apoptose/fisiologia , Progressão da Doença , Quimiocina CCL2/genética , Metaloproteinase 3 da Matriz/metabolismo , Condrócitos/enzimologia , Ácido Iodoacético , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Metaloproteinase 13 da Matriz/metabolismo , Receptores CCR2/antagonistas & inibidores , Receptores CCR2/genética , Fibroblastos/metabolismo , Proteínas Matrilinas/metabolismo , Camundongos Endogâmicos C57BL
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