The FX enzyme is a functional component of lymphocyte activation

被引:13
作者
Eshel, R
Besser, M
Zanin, A
Sagi-Assif, O
Witz, IP [1 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Dept Cell Res & Immunol, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Ela Kodesz Inst Res Canc Dev & Prevent, IL-69978 Tel Aviv, Israel
关键词
endothelial cells; cell-to-cell interaction; T cell activation; gene regulation; selectin ligands;
D O I
10.1006/cimm.2001.1872
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fucose is an essential constituent of selectin ligands. These molecules mediate the initial contact between extravasating leukocytes and endothelial cells. The generation of GDP-L-fucose by the FX enzyme is the final step of fucose biosynthesis. Recently, we demonstrated that outside-in signaling regulates the expression of the FX enzyme in certain cancer cells. The present study demonstrates that the polyclonal activation of T and B cells significantly up-regulated the expression of the FX enzyme and of the fucosylated selectin ligands sLe-x and CLA. Treatment of T cells with FX antisense oligonucleotides significantly decreased selectin ligand expression upon activation. We conclude that FX is regulated by outside-in signals also in lymphocytes and that this enzyme is involved in the biosynthesis of selectin ligands in such cells. We propose that FX takes part in the cascade of events leading to the extravasation of activated lymphocytes. (C) 2001 Elsevier Science (USA).
引用
收藏
页码:141 / 148
页数:8
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