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Differential expression of the complement regulatory proteins in the human eye
N S Bora1, C L Gobleman, J P Atkinson
1Department of Ophthalmology, Washington University School of Medicine, St. Louis, Missouri 63110.
Investigative Ophthalmology & Visual Science
|December 1, 1993
Summary
The human eye expresses membrane cofactor protein (MCP), decay accelerating factor (DAF), and membrane attack complex inhibiting protein (CD59). These proteins help protect eye tissues from complement-mediated damage during inflammation or infection.
Area of Science:
- Ophthalmology
- Immunology
- Cell Biology
Background:
- Complement activation products are present in the human eye during infection/inflammation.
- Host protection against self-tissue attack during complement activation is mediated by three membrane-bound complement regulatory proteins: membrane cofactor protein (MCP, CD46), decay accelerating factor (DAF, CD55), and membrane attack complex inhibiting protein (CD59).
Purpose of the Study:
- To analyze the expression of MCP, DAF, and CD59 in the normal human eye.
Main Methods:
- Human eye tissues were sectioned using a cryostat.
- Polyclonal and monoclonal antibodies against MCP, DAF, and CD59 were utilized for staining.
- Control stains included nonrelevant antibodies, normal rabbit serum, and omission of primary/secondary antibodies.
Main Results:
- All three complement regulatory proteins (MCP, DAF, CD59) showed differential expression in the human eye.
- MCP was strongly expressed in the corneal epithelium and weakly in corneal keratocytes and photoreceptor cells.
- DAF was highly expressed in the corneal epithelium and ciliary body, with moderate expression in corneal stroma and iris.
- CD59 demonstrated strong expression across the corneal epithelium, corneal stroma, iris, choroid, and all retinal layers, with moderate expression in the ciliary body.
Conclusions:
- The presence of MCP, DAF, and CD59 in the human eye indicates a regulatory system protecting ocular cells from complement-mediated destruction.
- Further research is needed to determine specialized functions of these proteins, particularly CD59 due to its widespread retinal expression.