- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Annual Issues
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
Clinical and Developmental Immunology
Volume 2013 (2013), Article ID 506807, 9 pages
O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin
1Unidad de Investigación, Instituto de Oftalmología Fundación Conde de Valenciana, 06800 México, DF, Mexico
2Laboratorio de Inmunología, Departamento de Bioquímica, Facultad de Medicina, (UNAM), P.O. Box 70159, 04510 México, DF, Mexico
3Departamento de Inmunología, Escuela Nacional de Ciencias Biológicas, IPN, 11340 México, DF, Mexico
4Departamento de Bioquímica, Instituto Nacional de Enfermedades Respiratorias, 4502 México, DF, Mexico
Received 18 June 2013; Accepted 4 August 2013
Academic Editor: Lenin Pavon
Copyright © 2013 María C. Jiménez-Martínez et al. 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.
- A. M. Wu, “Carbohydrate structural units in glycoproteins and polysaccharides as important ligands for Gal and GalNAc reactive lectins,” Journal of Biomedical Science, vol. 10, no. 6, pp. 676–688, 2003.
- S. Tsuboi and M. Fukuda, “Roles of O-linked oligosaccharides in immune responses,” BioEssays, vol. 23, pp. 46–53, 2001.
- N. Pineau, P. Aucouturier, J. C. Brugier, and J. L. Preud'homme, “Jacalin: a lectin mitogenic for human CD4 T lymphocytes,” Clinical and Experimental Immunology, vol. 80, no. 3, pp. 420–425, 1990.
- U. Chatterjee, P. P. Bose, S. Dey, T. P. Singh, and B. P. Chatterjee, “Antiproliferative effect of T/Tn specific Artocarpus lakoocha agglutinin (ALA) on human leukemic cells (Jurkat, U937, K562) and their imaging by QD-ALA nanoconjugate,” Glycoconjugate Journal, vol. 25, no. 8, pp. 741–752, 2008.
- H. Ohba, R. Bakalova, S. Moriwaki, and O. Nakamura, “Fractionation of normal and leukemic T-cells by lectin-affinity column chromatography,” Cancer Letters, vol. 184, no. 2, pp. 207–214, 2002.
- E. Zenteno, R. Lascurain, L. F. Montano, L. Vazquez, H. Debray, and J. Montreuil, “Specificity of Amaranthus leucocarpus lectin,” Glycoconjugate Journal, vol. 9, no. 4, pp. 204–208, 1992.
- A. Medeiros, S. Bianchi, J. J. Calvete et al., “Biochemical and functional characterization of the Tn-specific lectin from Salvia sclarea seeds,” European Journal of Biochemistry, vol. 267, no. 5, pp. 1434–1440, 2000.
- Y. Reisner, M. Linker Israeli, and N. Sharon, “Separation of mouse thymocytes into two subpopulations by the use of peanut agglutinin,” Cellular Immunology, vol. 25, no. 1, pp. 129–134, 1976.
- P. Hernández, M. Bacilio, F. Porras et al., “A comparative study on the purification of the Amaranthus leucocarpus syn. Hypocondriacus lectin,” Preparative Biochemistry and Biotechnology, vol. 29, no. 3, pp. 219–234, 1999.
- P. Hernández, D. Tetaert, G. Vergoten et al., “Specificity of Amaranthus leucocarpus syn. hypocondriacus lectin for O-glycopeptides,” Biochimica et Biophysica Acta, vol. 1674, no. 3, pp. 282–290, 2004.
- R. Lascurain, R. Chavez, P. Gorocica, A. Perez, L. F. Montano, and E. Zenteno, “Recognition of a CD4+ mouse medullary thymocyte subpopulation by Amaranthus leucocarpus lectin,” Immunology, vol. 83, no. 3, pp. 410–413, 1994.
- R. Lascurain, F. Porras, R. Báez et al., “Amaranthus leucocarpus lectin recognizes human naive T cell subpopulations,” Immunological Investigations, vol. 26, no. 5–7, pp. 579–587, 1997.
- E. Zenteno, J. L. Ochoa, C. Parra, M. Montaño, B. Ruíz, and R. Carvajal, “Machaerocereus eruca and Amaranthus leucocarpus lectins: biological activity on immune response cells,” in Lectins Biology, Biochemistry Clinical Chemistry, T. C. Bög-Hansen and J. Breborowicz, Eds., vol. 4, pp. 437–445, De Gruyter, Berlin, Germany, 1985.
- G. Alvarez, R. Lascurain, P. Hernández-Cruz et al., “Differential O-glycosylation in cortical and medullary thymocytes,” Biochimica et Biophysica Acta, vol. 1760, no. 8, pp. 1235–1240, 2006.
- X. Chen, T. Murakami, J. J. Oppenheim, and O. M. Z. Howard, “Differential response of murine CD4+CD25+ and CD4+CD25− T cells to dexamethasone-induced cell death,” European Journal of Immunology, vol. 34, no. 3, pp. 859–869, 2004.
- C. Karagiannidis, M. Akidis, P. Holopainen, et al., “Glucorticoids upregulate FOXP3 expression and regulatory T cells in asthma,” Journal of Allergy and Clinical Immunology, vol. 114, pp. 1425–1433, 2004.
- Y. Xie, M. Wu, R. Song et al., “A glucocorticoid amplifies IL-2-induced selective expansion of CD4+CD25+FOXP3+ regulatory T cells in vivo and suppresses graft-versus-host disease after allogeneic lymphocyte transplantation,” Acta Biochimica et Biophysica Sinica, vol. 41, no. 9, pp. 781–791, 2009.
- S. Sakaguchi, “Naturally arising CD4+ regulatory T cells for immunologic self-tolerance and negative control of immune responses,” Annual Review of Immunology, vol. 22, pp. 531–562, 2004.
- A. Toda and C. A. Piccirillo, “Development and function of naturally occurring CD4+CD25+ regulatory T cells,” Journal of Leukocyte Biology, vol. 80, no. 3, pp. 458–470, 2006.
- L. A. Stephens, C. Mottet, D. Mason, and F. Powrie, “Human CD4+CD25+ thymocytes and peripheral T cells have immune suppressive activity in vitro,” European Journal of Immunology, vol. 31, pp. 1247–1254, 2001.
- H. Yi, Y. Zhen, L. Jiang, J. Zheng, and Y. Zhao, “The phenotypic characterization of naturally occurring regulatory CD4+CD25+ T cells,” Cellular & Molecular Immunology, vol. 3, no. 3, pp. 189–195, 2006.
- P. Hoffmann, R. Eder, T. J. Boeld et al., “Only the CD45RA+ subpopulation of CD4+CD25 high T cells gives rise to homogeneous regulatory T-cell lines upon in vitro expansion,” Blood, vol. 108, no. 13, pp. 4260–4267, 2006.
- D. Valmori, A. Merlo, N. E. Souleimanian, C. S. Hesdorffer, and M. Ayyoub, “A peripheral circulating compartment of natural naive CD4+ Tregs,” Journal of Clinical Investigation, vol. 115, no. 7, pp. 1953–1962, 2005.
- J. Jenner, G. Kerst, R. Handgretinger, and I. Müller, “Increased alpha2,6-sialylation of surface proteins on tolerogenic, immature dendritic cells and regulatory T cells,” Experimental Hematology, vol. 34, no. 9, pp. 1212–1218, 2006.
- P. Van Den Steen, P. M. Rudd, R. A. Dwek, and G. Opdenakker, “Concepts and principles of O-linked glycosylation,” Critical Reviews in Biochemistry and Molecular Biology, vol. 33, no. 3, pp. 151–208, 1998.
- A. Golks, T.-T. T. Tran, J. F. Goetschy, and D. Guerini, “Requirement for O-linked N-acetylglucosaminyltransferase in lymphocytes activation,” EMBO Journal, vol. 26, no. 20, pp. 4368–4379, 2007.
- F. Urrea, B. Ortiz-Quintero, F. J. Sanchez-Garcia et al., “The Amaranthus leucocarpus lectin enhances the anti-CD3 antibody-mediated activation of human peripheral blood CD4+ T cells,” Tohoku Journal of Experimental Medicine, vol. 221, no. 4, pp. 271–279, 2010.
- D. Savage, G. Mattson, S. Desai, G. Nielander, S. Morgensen, and E. Conklin, Avidin-Biotin Chemistry. A Hand Book, Pierce Chemical Company, Rockford, Ill, USA, 1992.
- M. A. Daniels, K. A. Hogquist, and S. C. Jameson, “Sweet 'n' sour: the impact of differential glycosylation on T cell responses,” Nature Immunology, vol. 3, no. 10, pp. 903–910, 2002.
- J. J. Priatel, D. Chui, N. Hiraoka et al., “The ST3Gal-I sialyltransferase controls CD8+ T lymphocyte homeostasis by modulating O-glycan biosynthesis,” Immunity, vol. 12, no. 3, pp. 273–283, 2000.
- B. Ortíz, F. Porras, M. C. Jiménez-Martínez et al., “Differential expression of a 70 kDa O-glycoprotein on T cells: a possible marker for naive and early activated murine T cells,” Cellular Immunology, vol. 218, no. 1-2, pp. 34–45, 2002.
- N. Seddiki, B. Santner-Nanan, S. G. Tangye et al., “Persistence of naive CD45RA+ regulatory T cells in adult life,” Blood, vol. 107, no. 7, pp. 2830–2838, 2006.
- R. C. Duggleby, T. N. F. Shaw, L. B. Jarvis, G. Kaur, and J. S. Hill Gaston, “CD27 expression discriminates between regulatory and non-regulatory cells after expansion of human peripheral blood CD4+ CD25+ cells,” Immunology, vol. 121, no. 1, pp. 129–139, 2007.
- J. J. A. Coenen, H. J. P. M. Koenen, E. Van Rijssen, L. B. Hilbrands, and I. Joosten, “Rapamycin, and not cyclosporin A, preserves the highly suppressive CD27+ subset of human CD4+CD25+ regulatory T cells,” Blood, vol. 107, no. 3, pp. 1018–1023, 2006.
- E. M. Shevach, R. A. DiPaolo, J. Andersson, D.-M. Zhao, G. L. Stephens, and A. M. Thornton, “The lifestyle of naturally occurring CD4+CD25+Foxp3+ regulatory T cells,” Immunological Reviews, vol. 212, pp. 60–73, 2006.
- F. Sallusto, D. Lenig, R. Förster, M. Lipp, and A. Lanzavecchia, “Two subsets of memory T lymphocytes with distinct homing potentials and effector functions,” Nature, vol. 401, no. 6754, pp. 708–712, 1999.
- M.-L. Alegre, P. J. Noel, B. J. Eisfelder et al., “Regulation of surface and intracellular expression of CTLA4 on mouse T cells,” Journal of Immunology, vol. 157, no. 11, pp. 4762–4770, 1996.
- B. Fritzsching, N. Oberle, E. Pauly et al., “Naive regulatory T cells: a novel subpopulation defined by resistance toward CD95L-mediated cell death,” Blood, vol. 108, no. 10, pp. 3371–3378, 2006.