1.DNA Microarray-Based Gene Expression Profiling in Porcine Keratocytes and Corneal Endothelial Cells and Comparative Analysis Associated with Xeno-related Rejection.
Mee Kum KIM ; Joo Youn OH ; Jung Hwa KO ; Hyun Ju LEE ; Jin Ho JUNG ; Won Ryang WEE ; Jin Hak LEE ; Chung Gyu PARK ; Sang Joon KIM ; Curie AHN ; Seung Jun KIM ; Seung Yong HWANG
Journal of Korean Medical Science 2009;24(2):189-196
Porcine to rat corneal xenotransplantation resulted in severe inflammation and rejection of the corneal stroma, whereas an allograft showed mainly endothelial cell-associated rejection. We, therefore, investigated and compared the gene expression between porcine keratocytes and corneal endothelial cells. RNA was isolated from primary cultured porcine or human keratocytes and porcine corneal endothelial cells. Gene expression was comparatively analyzed after normalization with microarray method using Platinum pig 13 K oligo chip (GenoCheck Co., Ltd., Ansan, Korea). Real-time polymerase chain reaction (PCR) was performed for C1R, CCL2, CXCL6, and HLA-A in porcine keratocytes and corneal endothelial cells. As a result, upregulated expression more than 2 folds was observed in 1,162 genes of porcine keratocytes versus porcine endothelial cells. Among the immune-regulatory genes, SEMA3C, CCL2, CXCL6, F3, HLA-A, CD97, IFI30, C1R, and G1P3 were highly expressed in porcine keratocytes, compared to porcine corneal endothelial cells or human keratocytes. When measured by real-time PCR, the expression of C1R, CCL2, and HLA-A was higher in porcine keratocytes compared to that in porcine corneal endothelial cells. In conclusion, the increased expression of C1R, CCL2, and HLA-A genes in porcine keratocytes might be responsible for the stromal rejection observed in a porcine to rat corneal xenotransplantation.
Animals
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Cells, Cultured
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Chemokine CCL2/metabolism
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Complement C1r/metabolism
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Corneal Transplantation/*immunology/pathology
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Endothelium, Corneal/*metabolism/pathology
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*Gene Expression Profiling
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Graft Rejection/*immunology/pathology
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HLA-A Antigens/metabolism
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Humans
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Keratinocytes/*metabolism
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Oligonucleotide Array Sequence Analysis
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Rats
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Reverse Transcriptase Polymerase Chain Reaction
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Swine
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Transplantation, Heterologous
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Up-Regulation
2.The Role of Cyclosporine and Mycophenolate in an Orthotopic Porcine-to-Rat Corneal Xenotransplantation.
Hyeon Il LEE ; Mee Kum KIM ; Joo Youn OH ; Jung Hwa KO ; Hyun Ju LEE ; Won Ryang WEE ; Jin Hak LEE
Journal of Korean Medical Science 2008;23(3):492-501
We performed this study to investigate the feature of rejection in porcine-to-rat corneal orthotopic transplantation and to evaluate the effect of cyclosporine and mycophenolate on the xeno-rejection. Orthotopic corneal transplantation was done at 91 Sprague-Dawley rats, and they were divided into 10 groups based on the combination of immunosuppressants including dexamethasone, cyclosporine, and mycophenolate mofetil. Graft survival was analyzed and grafted eyes were examined with Hematoxylin & Eosin and CD4 or CD8 staining. Enzyme-linked immunosorbent assays were done for interleukin-2 (IL-2), IL-4, IL-5, IL-10, and interferon (IFN)-gamma in cornea, lacrimal gland, and cervical lymph nodes. The longest median survival of the immune suppressant group was 11.00+/-1.96 days, which showed no statistical differences compared with that of control (8.00+/-1.52 days). The neutrophils were prominent in the early phase but soon gave way to the monocytes. The number of CD8+ cells was higher than that of CD4+ cells. IL-2 and IFN-gamma markedly increased at 10 to13 days in cornea, lacrimal glands, and cervical lymph nodes, which showed a decrease with immunosuppressants except in the cornea. In conclusion, cyclosporine and mycophenolate could not prevent the rejection in porcine to rat orthotopic corneal xenograft associated with infiltraton of CD8+ and innate immune cells.
Animals
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*Corneal Transplantation
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Cyclosporine/*pharmacology
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Cytokines/metabolism
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Graft Rejection/immunology/pathology/*prevention & control
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Graft Survival/*drug effects
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Immunosuppressive Agents/*pharmacology
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Interferon-gamma/metabolism
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Interleukin-10/metabolism
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Interleukin-2/metabolism
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Interleukin-4/metabolism
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Interleukin-5/metabolism
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Mycophenolic Acid/*analogs & derivatives/pharmacology
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Neutrophils/immunology
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Rats
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Rats, Sprague-Dawley
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Swine
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Transplantation, Heterologous