Target cell susceptibility to lysis by human natural killer cells is augmented by α(1,3)-galactosyltransferase and reduced by α(1,2)-fucosyltransferase

被引:48
作者
Artrip, JH
Kwiatkowski, P
Michler, RE
Wang, SF
Tugulea, S
Ankersmit, J
Chisholm, L
McKenzie, IFC
Sandrin, MS
Itescu, S
机构
[1] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
[2] Austin Hosp, Heidelberg, Vic 3084, Australia
关键词
D O I
10.1074/jbc.274.16.10717
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Susceptibility of porcine endothelial cells to human natural killer (NK) cell lysis was found to reflect surface expression of ligands containing Gal alpha(1,3)GlcNAc, the principal antigen on porcine endothelium recognized by xenoreactive human antibodies. Genetically modifying expression of this epitope on porcine endothelium by transfection with the alpha(1,2)-fucosyltransferase gene reduced susceptibility to human NK lysis, These results indicate that surface carbohydrate remodeling profoundly affects target cell susceptibility to NK lysis, and suggest that successful transgenic strategies to limit xenograft rejection by NK cells and xenoreactive antibodies will need to incorporate carbohydrate remodeling.
引用
收藏
页码:10717 / 10722
页数:6
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