Analysis of chemokine receptor CCR7 expression on porcine blood T lymphocytes using a CCL19-Fc fusion protein
► Generation of cell lines expressing porcine CCR7 and CCL19. ► Use of CCL19-Fc fusion protein to analyze CCR7 expression in swine. ► CCR7 expression discriminates T cell subsets with naïve and memory features in swine. The chemokine receptor CCR7 has been a useful marker for the characterization of...
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Published in: | Developmental and comparative immunology Vol. 39; no. 3; pp. 207 - 213 |
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Main Authors: | , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
Elsevier Ltd
01-03-2013
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Subjects: | |
Online Access: | Get full text |
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Summary: | ► Generation of cell lines expressing porcine CCR7 and CCL19. ► Use of CCL19-Fc fusion protein to analyze CCR7 expression in swine. ► CCR7 expression discriminates T cell subsets with naïve and memory features in swine.
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 naïve phenotype, whereas the 2E3− cells were mostly negative. Among CD8+ T cells CCL19-Fc labelled two subsets: one, CD8βhi CD11alo CD45RA+, perforin−/lo , which produced low amounts of IFN-γ after stimulation, which might correspond to naïve cells; and a second small population of CD8βlo cells which expressed high levels of CD11a, and were mostly CD45RA−, a phenotype which resembles that of human central memory T cells. |
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Bibliography: | http://dx.doi.org/10.1016/j.dci.2012.11.010 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0145-305X 1879-0089 |
DOI: | 10.1016/j.dci.2012.11.010 |