Elsevier

Laboratory Investigation

Volume 83, Issue 4, 1 April 2003, Pages 579-588
Laboratory Investigation

Article
Role of Macrophage Inflammatory Protein-3α and Its Ligand CCR6 in Rheumatoid Arthritis

https://doi.org/10.1097/01.LAB.0000062854.30195.52Get rights and content
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Abstract

We examined the expression and participation of CCR6 and its ligand MIP-3α in rheumatoid arthritis (RA) by ELISA, RT-PCR, real-time PCR (TaqMan) analysis, monocyte chemotaxis, and two- and four-color flow cytometry. We found that RA synovial fluid (SF) contained significantly more MIP-3α than osteoarthritis (OA), indicating a potential role for MIP-3α in RA. IL-1β, IL-18, and TNF-α stimulated RA fibroblast MIP-3α production at 48 hours of incubation in vitro. By TaqMan analysis, there were more CCR6 mRNA transcripts in RA synovial tissue (ST) than in OA or normal (NL) ST, and elevated MIP-3α mRNA expression in RA compared with NL ST. By FACS analysis, there were significantly elevated percentages of CD3+/CD4+/CD45RO+/CCR6+ memory lymphocytes found in RA peripheral blood (PB) compared with NL PB or RA SF. We also found that MIP-3α induced monocyte chemotactic activity at 1.25 pm, consistent with concentrations of MIP-3α found in RA SF. Furthermore, MIP-3α accounted for 40% of RA SF chemotactic activity for monocytes in modified Boyden chamber assays. We confirmed that MIP-3α may be binding a G-coupled protein receptor because in vitro monocyte chemotaxis was inhibited by preincubation of monocytes with pertussis toxin. RA patient clinical data revealed that CD3+ lymphocyte/CCR6 expression inversely correlated with the age of the patient, indicating that CCR6 expression may be important in the development of RA at a younger age. Overall, these studies indicate that MIP-3α and CCR6 may function to recruit monocytes and memory lymphocytes from the RA PB to the RA joint. These results further indicate that expression of CCR6, the receptor for MIP-3α, can be correlated with RA development.

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