Elsevier

Experimental Eye Research

Volume 63, Issue 3, September 1996, Pages 297-303
Experimental Eye Research

Regular article
Interleukin-7 (IL-7) Induces Retinal Pigment Epithelial Cell MCP-1 and IL-8

https://doi.org/10.1006/exer.1996.0118Get rights and content

Abstract

The neuroectodermally-derived retinal pigment epithelium (RPE) forms part of the blood–retina barrier where it is strategically-positioned to regulate leukocyte infiltration in retinal diseases. Activated human RPE cells possess several functions enabling them to perform this role including expression of HLA-DR antigens, production of intercellular adhesion molecule-1, and secretion of monocyte chemotactic protein-1 and interleukin-8. In this study, we examined the ability of interleukin-7 to induce RPE-derived monocyte chemotactic protein-1 and interleukin-8 and assessed the potentiating effects of interleukin-7 on interleukin-1β- and tumor necrosis factor-α-induced RPE monocyte chemotactic protein-1 and interleukin-8 production. Human RPE cells incubated with interleukin-7 (1–100 ng ml−1) for 24 hr secreted significant levels of antigenic RPE monocyte chemotactic protein-1 and interleukin-8 in a dose-dependent fashion interleukin-7 (P<0.05). RPE costimulation with interleukin-7 and interleukin-1β (2 ng ml−1) or tumor necrosis factor-α(2 ng ml−1) resulted in additive increases (P<0.05) in secreted monocyte chemotactic protein-1 and interleukin-8. Steady-state RPE monocyte chemotactic protein-1 mRNA was substantially increased by interleukin-7 (1–100 ng ml−1), while RPE interleukin-8 mRNA was mildly elevated by higher doses of interleukin-7 (10–100 ng ml−1). Time-dependent increases in RPE monocyte chemotactic protein-1 and interleukin-8 mRNA were noted. RPE monocyte chemotactic protein-1 mRNA peaked at 2 hr and decreased over 8 hr and 24 hr. Whereas, RPE interleukin-8 mRNA was perceptible at 2 hr, maximal at 8 hr, and reduced by 24 hr. Interleukin-7 potentiated interleukin-1β-induced monocyte chemotactic protein-1 and interleukin-8 steady-state mRNA expression at all interleukin-7 concentrations. Interleukin-7 potentiated tumor necrosis factor-α-induced RPE monocyte chemotactic protein-1 steady-state mRNA expression at all doses of interleukin-7 while only high dose interleukin-7 (100 ng ml−1) enhanced tumor necrosis factor-α-induced RPE interleukin-8 steady-state gene expression. Our data show that interleukin-7 is a primary stimulus of RPE monocyte chemotactic protein-1 and interleukin-8. This is one of the first reports demonstrating: (1) interleukin-7 induction of monocyte chemotactic protein-1 in any cell type, and (2) interleukin-7 induction of interleukin-8 in resident, tissue-based cells. These studies suggest that interleukin-7 potentiation of interleukin-1βand tumor necrosis factor-α-induced RPE monocyte chemotactic protein-1 and IL-8 may be important for the elicitation of leukocyte chemotaxins in diseased retinal tissue when only low ambient levels of individual pro-inflammatory cytokines are present.

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For correspondence at: Department of Ophthalmology, University of Michigan, Kellogg Eye Center, 1000 Wall St., Ann Arbor, MI 48105, U.S.A.

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