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Published on: August 20, 2016
Immunological features of human corneal endothelial cells
1Department of Ophthalmology, University of Hamburg, Hamburg, Germany. fanwang_hh@yahoo.com
Insights
Human corneal endothelial cells (HCEC) function as antigen-presenting cells, activating T lymphocytes. This suggests HCEC play a role in corneal transplant rejection.
Area of Science:
- Immunology
- Ophthalmology
- Cell Biology
Background:
- Human corneal endothelial cells (HCEC) are crucial for corneal clarity.
- Their role in immune responses, particularly in transplantation, is not fully understood.
Purpose of the Study:
- To investigate the immunological function of HCEC.
- To determine if HCEC can act as antigen-presenting cells.
Main Methods:
- Immunohistochemical analysis of HLA-DP, -DQ, -DR, CD40, CD80, and CD86 expression on HCEC.
- Co-culture of HCEC with peripheral blood mononuclear cells (PBMCs).
- Assessment of lymphocyte activation using fluorescence-activated cell sorting (FACS) analysis, with and without gamma-interferon (IFN) pretreatment of HCEC.
Main Results:
- HCEC demonstrated the ability to activate T lymphocytes in a co-culture system.
- Gamma-interferon (IFN) pretreatment significantly increased the expression of HLA-DP, -DQ, -DR, and CD40 on HCEC.
- Costimulatory molecule CD80 was expressed on HCEC.
Conclusions:
- HCEC possess characteristics of antigen-presenting cells.
- HCEC may contribute to the immune rejection of corneal transplants.
- These findings highlight the immunological relevance of HCEC in ocular transplantation.
Purpose:
To investigate the function of human corneal endothelial cells (HCEC) as immunological cells.
Methods:
Expression of HLA-DP, -DQ, -DR, CD40, CD80 and CD86 was determined by immunohistochemical methods. Purified peripheral blood mononuclear cells were cocultured with HCEC, part of which had been pretreated with gamma-interferon (IFN), and activation of lymphocytes was determined by fluorescence-activated cell sorting analysis.
Results:
In the coculture system, T lymphocytes were activated by corneal endothelial cells; HLA-DP, -DQ, -DR and CD40 expressions were increased by gamma-IFN pretreatment. Costimulatory CD80 was shown on the endothelial cells.
Conclusions:
HCEC can be assumed to be involved in the rejection process of corneal transplants as potential antigen-presenting cells.
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