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From the Department of Microbiology and Immunology, University of South Alabama, College of Medicine, Mobile, Alabama.
PURPOSE. The purpose of this study was to determine whether human corneal epithelial cells and keratocytes synthesize both the soluble and membrane forms of the type II IL-1 receptor (IL-1RII).
METHODS. Primary cell cultures of human corneal epithelial cells and keratocytes
were established from human corneas. RT-PCR was used to analyze cell
cultures for expression of IL-1RII mRNA. The capacity of corneal cells
to synthesize membrane-bound IL-1RII was determined by
immunofluorescence microscopy, whereas ELISA was used to quantitate
synthesis of soluble IL-1RII after IL-1
and TNF-
stimulation.
RESULTS. Corneal epithelial cells expressed IL-1RII mRNA. The cells also stained
positive for membrane-bound IL-1RII, and media harvested from
epithelial cell cultures contained up to 50 pg/ml of soluble IL-1RII.
Both IL-1
and TNF-
significantly enhanced the amounts of soluble
IL-1RII released from epithelial cell surfaces. In contrast to
epithelial cells, corneal keratocytes did not express IL-1RII mRNA.
Membrane-bound IL-1RII was not detected on keratocytes, nor was soluble
IL-1RII detected in culture media harvested from these cells.
CONCLUSIONS. Human corneal epithelial cells but not corneal keratocytes synthesize
both membrane and soluble forms of IL-1RII. Because both forms of
IL-1RII can function as IL-1
antagonists, the results suggest that
human corneal epithelial cells but not corneal keratocytes have evolved
the capacity to dampen IL-1
responses through the production of
IL-1RII.
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