Analysis of chemokine receptor CCR7 expression on porcine blood T lymphocytes using a CCL19-Fc fusion protein

被引:16
作者
Moreno, S. [1 ]
Alvarez, B. [1 ]
Martinez, P. [1 ]
Uenishi, H. [2 ]
Revilla, C. [1 ]
Ezquerra, A. [1 ]
Alonso, F. [1 ]
Dominguez, J. [1 ]
机构
[1] INIA, Dpto Biotecnol, Madrid 28040, Spain
[2] NIAS, Ibaraki, Japan
关键词
Swine; Chemokines; CCL19; CCR7; T cell subsets; DIFFERENTIAL EXPRESSION; EBI1-LIGAND CHEMOKINE; DENDRITIC CELL; CUTTING EDGE; IN-VIVO; B-CELLS; MEMORY; EFFECTOR; SUBSETS; NAIVE;
D O I
10.1016/j.dci.2012.11.010
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The chemokine receptor CCR7 has been a useful marker for the characterization of human and mouse T cell subsets. We have produced the porcine CCR7 ligand CCL19 fused to the human IgG1 Fc fragment, and used it to analyse CCR7 expression in swine. CCL19-Fc bound to and induced the migration of cells expressing porcine CCR7 but not of untransfected cells, corroborating its specificity. On blood lymphocytes, CCL19-Fc labelled the majority of CD4(+) T cells expressing the 2E3 marker, associated with a nave phenotype, whereas the 2E3(-) cells were mostly negative. Among CD8(+) T cells CCL19-Fc labelled two subsets: one, CD8 beta(hi) CD11a(lo) CD45RA(+), perforin(-/lo), which produced low amounts of IFN-gamma after stimulation, which might correspond to nave cells; and a second small population of CD8 beta(lo) cells which expressed high levels of CD11a, and were mostly CD45RA(-), a phenotype which resembles that or human central memory T cells. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:207 / 213
页数:7
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