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Safe disposal of inflammatory urate crystals by differentiated macrophages

Landis, R.C., Yagnik, D., Emons, V., Philippidis, P., Mason, J.C., and Haskard, D.O.

Clive Landis

Arthritis & Rheumotology






Objective Although monosodium urate monohydrate (MSU) crystals have been recognized since the 18th century as the etiologic agent of gout, it is still unknown why certain hyperuricemic individuals remain asymptomatic, and how an acute attack of gout spontaneously resolves. We hypothesized that mononuclear phagocytes hold the key to these questions, and that the state of monocyte/macrophage differentiation is critical. Methods Human peripheral blood monocytes were differentiated for 1–7 days in vitro and examined with respect to 1) uptake of MSU crystals, 2) expression of macrophage, dendritic cell, and activation markers, 3) secretion of tumor necrosis factor ? (TNF?), interleukin 1? (IL?1?), IL?6, and IL?10, 4) activation of endothelial E?selectin expression, and 5) enhancement of secondary neutrophil recruitment by endothelial cells. Results MSU crystals induced TNF?, IL?1?, and IL?6 (but not IL?10) secretion in undifferentiated monocytes, which in turn promoted endothelial cell E?selectin expression and secondary neutrophil capture under shear flow. In contrast, differentiation over 3–5 days led to development of a noninflammatory phenotype characterized by a lack of proinflammatory cytokine secretion, lack of endothelial cell activation, and lack of secondary neutrophil recruitment. Acquisition of the noninflammatory phenotype correlated with expression of macrophage antigen but not with expression of dendritic cell marker or activation marker. Monocytes and macrophages were similarly phagocytic, and a control particle, zymosan, elicited secretion of the full panel of cytokines in both cell types. However, coincubation with MSU led to a significant suppression of zymosan?induced TNF? secretion (P = 0.009) from macrophages but not monocytes. Conclusion These findings imply that differentiated macrophages provide a safe?disposal mechanism for the removal of inflammatory urate crystals. This may be of clinical relevance to the maintenance of asymptomatic hyperuricemia and the resolution of acute gout.


American College of Rheumatology


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