IL-4 potentiates IL-1 beta- and TNF-alpha-stimulated IL-8 and MCP-1 protein production in human retinal pigment epithelial cells

Purpose. Human retinal pigment epithelial (HRPE) cells are involved in ocul ar inflammation by secretion of chemokines such as IL-8 and MCP-1. It has b een shown in this and other laboratories that interleukin-1 beta (IL-1 beta ) and tumor necrosis factor-alpha (TNF-alpha) are potent inducers of HRPE I L-8 and MCP-1 secretion. The induced IL-8 and MCP-1 expression is often mod ulated by other proinflammatory factors in a synergistic manner. Modulation of IL-8 and MCP-1 production by interleukin-4 (IL-4), a important mediator in Th2-mediated immunity, and granulocyte/macrophage-colony-stimulating fa ctor (GM-CSF), one of the cytokines secreted by HRPE has been reported in n on-ocular cells. The aim of the present investigation was to study effects of these two cytokines alone or in combination with IL-1 beta or TNF-alpha on HRPE IL-8 and MCP-1 generation. Methods. The primary culture of HRPE cells was stimulated with various dose s of IL-4, GM-CSF, IL1-beta and TNF-alpha alone or in combination for 8 or 24 hr. The supernatants were subjected to enzyme-linked immunosorbent assay (ELISA) for IL-8 and MCP-I. The mRNAs were isolated from the corresponding cells for Northern blot analysis. Results. IL-1 beta and TNF-alpha induced dose-dependent increases in HRPE I L-8 and MCP-1 secretion with maximal stimulation observed at 2-5 ng/ml. IL- 4 alone (100 ng/ml) resulted in a slight increase of MCP-1 and IL-8 secreti on. When IL-4 was co-administrated with IL-1 beta or TNF-alpha, two to thre efold increases in IL-8 and MCP-1 were observed over the maximal levels ind uced by IL-1 beta or TNF-alpha alone. Northern blot analyses revealed that 1L-4 did not alter the steady-state MCP-1 mRNA stimulated by IL-1 beta and TNF-alpha, or alter the IL-8 mRNA stimulated by TNF-alpha, although the IL- 1 beta-induced IL-s mRNA was slightly enhanced by higher concentrations of IL-4 (100 ng/ml). Conclusion. The synergistic action by IL-4 occurs predominately at the post -transcriptional level. In contrast to IL-4, GM-CSF alone or in combination with IL-1 beta or TNF-alpha did not generate additional secretion of HRPE IL-8 and MCP-1. HRPE IL-8 and MCP-1 gene expression and protein production are stimulated by IL-1 beta or TNF-alpha through pathways differentially mo dulated by 1L-4 and GM-CSF.