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Susceptibility of porcine keratocytes to immune-mediated damage in xeno-related rejection

Cited 7 time in Web of Science Cited 7 time in Scopus
Authors

Kim, M. K.; Oh, J. Y.; Lee, H. I.; Ko, J. H.; Lee, H. J.; Lee, J. H.; Wee, W. R.

Issue Date
2008-03
Publisher
Appleton & Lange
Citation
Transplantation Proceedings, Vol.40 No.2, pp.564-569
Abstract
We admixed cultured porcine keratocytes or corneal endothelial cells in the presence of human sera or peripheral blood mononuclear cells (PBMCs) for 4 to 72 hours to investigate their immune-related susceptibilities to xeno-related rejection. We evaluated complement deposition at 48 hours by flow cytometry after staining with the C3 anti-goat cy3 antibody. The inhibition of proliferation of porcine corneal cells by human sera was examined using the 3-[4,5-dimethy/thiazol-2,5-dephenyl tetrazolium bromide (MTT) assay over 24 to 72 hours. The amount of (51)chromium (Cr)-release was estimated after a reaction between the porcine cells and human PBMCs for 4 hours. There was greater C3 deposition in keratocytes (60.2%) than in endothelial cells (26.9%; P = .05, Mann-Whitney U test). Both keratocytes and endothelial cells showed significant levels of proliferative inhibition over a period of 72 hours. The number of Cr-51-release cells on interleukin-2 addition was significantly higher among keratocytes (88.0%) than endothelial cells (51.4%) at a 1:100 target:effector ratio (P = .04, Mann-Whitney U test). Our present data suggested that porcine keratocytes might be key target cells in xeno-related rejections when the porcine cornea is transplanted to primates.
ISSN
0041-1345
URI
https://hdl.handle.net/10371/191691
DOI
https://doi.org/10.1016/j.transproceed.2007.12.024
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