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O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin
O-glycosidically-linked glycans have been involved in development, maturation, homing, and immune regulation in T cells. Previous reports indicate that Amaranthus leucocarpus lectin (ALL), specific for glycans containing galactose-N-acetylgalactosamine and N-acetylgalactosamine, recognizes human naï...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794550/ https://www.ncbi.nlm.nih.gov/pubmed/24174970 http://dx.doi.org/10.1155/2013/506807 |
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author | Jiménez-Martínez, María C. Lascurain, Ricardo Méndez-Reguera, Aniela Estrada-Parra, Sergio Estrada-García, Iris Gorocica, Patricia Martínez-Cairo, Salvador Zenteno, Edgar Chávez, Raúl |
author_facet | Jiménez-Martínez, María C. Lascurain, Ricardo Méndez-Reguera, Aniela Estrada-Parra, Sergio Estrada-García, Iris Gorocica, Patricia Martínez-Cairo, Salvador Zenteno, Edgar Chávez, Raúl |
author_sort | Jiménez-Martínez, María C. |
collection | PubMed |
description | O-glycosidically-linked glycans have been involved in development, maturation, homing, and immune regulation in T cells. Previous reports indicate that Amaranthus leucocarpus lectin (ALL), specific for glycans containing galactose-N-acetylgalactosamine and N-acetylgalactosamine, recognizes human naïve CD27(+)CD25(+)CD4(+) T cells. Our aim was to evaluate the phenotype of CD4(+) T cells recognized by ALL in peripheral blood mononuclear cells obtained from healthy volunteers. CD4(+) T cells were isolated by negative selection using magnetic beads-labeled monoclonal antibodies; the expression of T regulatory cell phenotypic markers was assessed on ALL-recognized cells. In addition, IL-4, IL-10, IFN-γ, and TGF-β intracellular production in ALL (+) cells was also evaluated. The analyses of phenotypic markers and intracellular cytokines were performed through flow cytometry. ALL-recognized CD4(+) T cells were mainly CD45RA(+), CCR7(+) cells. Although 52 ± 10% CD25(+)Foxp3(+) cells were positive to ALL, only 34 ± 4% of ALL (+) cells corresponded to CD25(+)Foxp3(−) cells. Intracellular cytokines in freshly obtained ALL (+)CD4(+) T cells exhibited 8% of IL-4, 15% of IL-10, 2% of IFN-γ, and 15% of TGF-β, whereas ALL (−)CD4(+) T cells depicted 1% of IL-4, 2% of IL-10, <1% of IFN-γ, and 6% of TGF-β. Our results show that galactose-N-acetylgalactosamine and N-galactosamine-bearing CD4(+) T cells expressed phenotypic markers of NnTreg cells. |
format | Online Article Text |
id | pubmed-3794550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-37945502013-10-30 O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin Jiménez-Martínez, María C. Lascurain, Ricardo Méndez-Reguera, Aniela Estrada-Parra, Sergio Estrada-García, Iris Gorocica, Patricia Martínez-Cairo, Salvador Zenteno, Edgar Chávez, Raúl Clin Dev Immunol Research Article O-glycosidically-linked glycans have been involved in development, maturation, homing, and immune regulation in T cells. Previous reports indicate that Amaranthus leucocarpus lectin (ALL), specific for glycans containing galactose-N-acetylgalactosamine and N-acetylgalactosamine, recognizes human naïve CD27(+)CD25(+)CD4(+) T cells. Our aim was to evaluate the phenotype of CD4(+) T cells recognized by ALL in peripheral blood mononuclear cells obtained from healthy volunteers. CD4(+) T cells were isolated by negative selection using magnetic beads-labeled monoclonal antibodies; the expression of T regulatory cell phenotypic markers was assessed on ALL-recognized cells. In addition, IL-4, IL-10, IFN-γ, and TGF-β intracellular production in ALL (+) cells was also evaluated. The analyses of phenotypic markers and intracellular cytokines were performed through flow cytometry. ALL-recognized CD4(+) T cells were mainly CD45RA(+), CCR7(+) cells. Although 52 ± 10% CD25(+)Foxp3(+) cells were positive to ALL, only 34 ± 4% of ALL (+) cells corresponded to CD25(+)Foxp3(−) cells. Intracellular cytokines in freshly obtained ALL (+)CD4(+) T cells exhibited 8% of IL-4, 15% of IL-10, 2% of IFN-γ, and 15% of TGF-β, whereas ALL (−)CD4(+) T cells depicted 1% of IL-4, 2% of IL-10, <1% of IFN-γ, and 6% of TGF-β. Our results show that galactose-N-acetylgalactosamine and N-galactosamine-bearing CD4(+) T cells expressed phenotypic markers of NnTreg cells. Hindawi Publishing Corporation 2013 2013-09-24 /pmc/articles/PMC3794550/ /pubmed/24174970 http://dx.doi.org/10.1155/2013/506807 Text en Copyright © 2013 María C. Jiménez-Martínez et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Jiménez-Martínez, María C. Lascurain, Ricardo Méndez-Reguera, Aniela Estrada-Parra, Sergio Estrada-García, Iris Gorocica, Patricia Martínez-Cairo, Salvador Zenteno, Edgar Chávez, Raúl O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title | O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title_full | O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title_fullStr | O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title_full_unstemmed | O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title_short | O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin |
title_sort | o-glycosylation of nntreg lymphocytes recognized by the amaranthus leucocarpus lectin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3794550/ https://www.ncbi.nlm.nih.gov/pubmed/24174970 http://dx.doi.org/10.1155/2013/506807 |
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