Structure/function characterization of porcine CD59: Expression, chromosomal mapping, complement-inhibition and costimulatory activity

Stephen E. Maher, David L. Pflugh, Niels J. Larsen, Max F. Rothschild, Alfred L.M. Bothwell

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Background. Complement regulatory proteins have become important targets to potentially modulate inflammatory reactions or transplant rejection. Since pig into human xenotransplantation could potentially overcome the enormous shortage of donor organs and tissues, characterization of porcine complement regulatory proteins is critical. Methods. The porcine CD59 cDNA has been isolated from porcine aortic endothelial cells and its structure determined. In addition, a molecular genetic analysis of the gene and its transcriptional properties and a functional analysis have been performed utilizing the transfected cDNA. Results. The most prominent mRNA species is 1.8 kilobases but cloned reverse transcriptase polymerase chain reaction products suggest that multiple polyadenylation sites are utilized. Gene mapping was performed utilizing a polymorphism identified in the 3' UT, and the gene was localized to within 3 cM of follicle-stimulating hormone, beta polypeptide in the middle of the chromosome 2 linkage map. RNA expression was equivalent in endothelial, kidney, and testis cell lines. Comparisons have been made with CD59 sequences from other species to identify possible important domains of the protein. The cDNA has been utilized to express an epitope-tagged or wild- type protein either transiently on COS-7 cells or stably in Chinese hamster ovary cells. The porcine CD59 protein effectively inhibited the antibody- mediated lytic activity of both porcine and human complement. In contrast to human CD59, porcine CD59 is incapable of providing costimulation to human T cells. Conclusions. These data suggest that overexpression of porcine CD59 might be more effective than human CD59 in prolonging xenograft survival with transgenic pig organs because of reduced immunoreactivity.

Original languageEnglish (US)
Pages (from-to)1094-1100
Number of pages7
JournalTransplantation
Volume66
Issue number8
DOIs
StatePublished - Oct 27 1998
Externally publishedYes

ASJC Scopus subject areas

  • Transplantation

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