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Abstracts (complete list) - Wissenschaft Online

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Silvia Capellino, Peter Angele, Werner Falk, Maurizio Cutolo, Rainer H. Straub<br />

Chromaffin-like cells and catecholamine production: role on<br />

the inflammatory response in rheumatoid arthritis (RA)<br />

patients<br />

Introduction: It is well known that norepinephrine (NE) influence the immune response.<br />

We already demonstrated that in RA synovial tissue there is a loss of sympathetic nerve<br />

fibers compared to osteoarthritis (OA). However, there is no difference in NE release<br />

from synovial tissue in both groups.<br />

Aim: To identify cells positive for tyrosine hydroxylase (TH) and PGP9.5 (neuronal<br />

marker) and to understand the role of the local catecholamine production during the<br />

inflammatory response in RA patients.<br />

Materials and methods: Synovial samples were obtained from OA and RA patients who<br />

underwent knee joint replacement surgery. Tissue samples were frozen and than<br />

analyzed for TH, PGP9.5 and synovial cell markers by doublestain-immunofluorescence.<br />

From the same patients, synovial cells were isolated by tissue enzymatic digestion, and<br />

cultured with Reserpine (10 -6 to 10 -8 M) or medium (control) for 24 hours.<br />

Determination of TNFα, IL-10, IL-8 and IL-6 was performed by Luminex technique and<br />

ELISA.<br />

Results: Only in RA we found cells expressing PGP9.5. These cells did not doublestain<br />

with markers for fibroblasts, macrophages, T-cells and B-cells but also express TH. The<br />

blockade of catecholamine release by Reserpine 10 -6 M caused a reduction of TNFα by<br />

60% compared to control cells in RA patients. In OA there was a reduced TNFα<br />

production in Reserpine-treated cells, but the effects were lower than in RA. The<br />

production of IL -6 and IL -8 tended to be lower in Reserpine-treated RA cells, but not in<br />

OA.<br />

Conclusions: We hypothesize that chromaffin-like cells are present in RA synovial tissue,<br />

producing NE and other catecholamines, and acting on local inflammation. Our future<br />

goal is to investigate the effects of the different catecholamines on the inflammatory<br />

reaction.

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