Literature DB >> 7539168

Tissue expression of human complement inhibitor, decay-accelerating factor, in transgenic pigs. A potential approach for preventing xenograft rejection.

A M Rosengard1, N R Cary, G A Langford, A W Tucker, J Wallwork, D J White.   

Abstract

Since complement-mediated hyperacute rejection of xenografts prevents the use of pigs as organ donors to man, the development of transgenic animals expressing species-specific complement inhibitors could provide a strategy for overcoming hyperacute rejection. The complement inhibitor, human decay-accelerating factor (hDAF), prevents the assembly of C3 and C5 convertases. In this article, the first histologic analysis of hDAF expression in pig tissues, specifically expression in endothelial cells of pigs transgenic for hDAF, is described. Twenty-seven transgenic pigs were categorized into 4 groups based on the expression patterns in endothelial, vascular smooth muscle, and squamous epithelial cells of skin biopsy specimens. Skin biopsy specimens permitted evaluation of the pigs without the need to kill them or to perform invasive procedures. Sixteen cases demonstrated endothelial cell staining. Complete necropsy evaluation, available in 14 of the 27 pigs, correlated with the skin biopsy specimen expression of hDAF. The immunoperoxidase data matched identically with the presence of the mRNA transcript in 25 of the 26 cases where RNA data were available. Also, the staining patterns of 6 transgenic pig founders and their 9 offspring (total of 9 founder-offspring pairs) correlated. Since transgenes are variably expressed in different cell types and since tissue lysates represent a melange of cell types, histologic evaluation for protein expression in tissues from transgenic animals will be critical if they are to be bred to become clinical organ donors. In addition to endothelial expression of hDAF, its expression on vascular smooth muscle cells may be important in preventing tissue damage when breaks in the endothelium occur.

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Year:  1995        PMID: 7539168

Source DB:  PubMed          Journal:  Transplantation        ISSN: 0041-1337            Impact factor:   4.939


  12 in total

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2.  The possible use of HLA-G1 and G3 in the inhibition of NK cell-mediated swine endothelial cell lysis.

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Journal:  Clin Exp Immunol       Date:  2001-10       Impact factor: 4.330

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Journal:  Cell Transplant       Date:  2017-02-03       Impact factor: 4.064

Review 4.  Clinical immunology.

Authors:  T E Mollnes; M Harboe
Journal:  BMJ       Date:  1996-06-08

5.  Analysis of transgene integration sites in transgenic pigs by fluorescence in situ hybridization.

Authors:  H W Kuipers; G A Langford; D J White
Journal:  Transgenic Res       Date:  1997-07       Impact factor: 2.788

Review 6.  Transgenesis in the rat and larger mammals.

Authors:  L J Mullins; J J Mullins
Journal:  J Clin Invest       Date:  1996-04-01       Impact factor: 14.808

7.  Generation of GTKO Diannan Miniature Pig Expressing Human Complementary Regulator Proteins hCD55 and hCD59 via T2A Peptide-Based Bicistronic Vectors and SCNT.

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Journal:  Mol Biotechnol       Date:  2018-08       Impact factor: 2.695

Review 8.  The role of genetically engineered pigs in xenotransplantation research.

Authors:  David K C Cooper; Burcin Ekser; Jagdeece Ramsoondar; Carol Phelps; David Ayares
Journal:  J Pathol       Date:  2015-10-07       Impact factor: 7.996

Review 9.  Murine mentors: transgenic and knockout models of surgical disease.

Authors:  J M Arbeit; R Hirose
Journal:  Ann Surg       Date:  1999-01       Impact factor: 12.969

Review 10.  Islet Xeno/transplantation and the risk of contagion: local responses from Canada and Australia to an emerging global technoscience.

Authors:  Myra Cheng
Journal:  Life Sci Soc Policy       Date:  2015-10-23
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