Amaranthus leucocarpus lectin (ALL) Enhances anti-CD3-Dependent Activation of Murine T Cells and Promotes Cell Survival

被引:7
作者
Urrea, Francisco [1 ]
Zenteno, Edgar [2 ]
Avila-Moreno, Federico [3 ]
Sanchez-Garcia, Francisco Javier [4 ]
Zuniga, Joaquin [5 ]
Lascurain, Ricardo [2 ]
Ortiz-Quintero, Blanca [1 ]
机构
[1] Inst Nacl Enfermedades Resp Ismael Cosio Villegas, Dept Bioquim, Mexico City 14080, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Fac Med, Dept Bioquim, Lab Inmunol, Mexico City 04510, DF, Mexico
[3] Inst Nacl Enfermedades Resp Ismael Cosio Villegas, Dept Microbiol, Mexico City 14080, DF, Mexico
[4] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Dept Inmunol, Mexico City 07738, DF, Mexico
[5] Inst Nacl Enfermedades Resp Ismael Cosio Villegas, Lab Inmunobiol & Genet, Mexico City 14080, DF, Mexico
关键词
Amaranthus leucocarpus; Lectins; Glycosylation; T-cell activation; DIFFERENTIAL EXPRESSION; AFFINITY-CHROMATOGRAPHY; IMMUNE-SYSTEM; P38; MAPK; GLYCOSYLATION; JACALIN; LYMPHOCYTES; GLYCANS; CD4(+); COSTIMULATION;
D O I
10.3109/08820139.2010.503767
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Gal beta 1,3GalNAc-specific lectin from Amaranthus leucocarpus (ALL) shows a differential binding pattern on murine thymocytes, peripheral and activated CD4<SU+</SU and CD8<SU+</SU T cells. Although ALL detects activation-related changes in T cell surface carbohydrate moieties, no study has been performed to examine the effect of ALL on T cell activation. In this study, we analyzed the anti-CD3-dependent activation of murine T cells in the presence of ALL by measuring proliferation, surface activation marker expression, and IL-2 secretion using total cells from the lymph node. The results showed that ALL did not significantly induce T cell activation but did enhance anti-CD3-dependent activation of both CD4<SU+</SU and CD8<SU+</SU T cells. In addition, ALL protected T cells from spontaneous apoptosis and increased cell survival in serum-free culture conditions. Our findings indicate that ALL alone does not affect T cell activation, but do suggest that ALL has an anti-CD3-dependent co-stimulatory-like effect on T cell activation. Moreover, ALL promotes cell survival in regular and serum-free culture conditions. This study is the first report of a non-mitogenic T cell-binding lectin that can induce a possible costimulatory-like effect and provides a new tool for understanding how glycosylation impacts the T cell response.</.
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页码:113 / 129
页数:17
相关论文
共 31 条
[1]  
Ashraf Mohd Tashfeen, 2003, Med Sci Monit, V9, pRA265
[2]   Glycosylation-dependent interaction of Jacalin with CD45 induces T lymphocyte activation and Th1/Th2 cytokine secretion [J].
Baba, Makoto ;
Ma, Bruce Yong ;
Nonaka, Motohiro ;
Matsuishi, Yukari ;
Hirano, Makoto ;
Nakamura, Natsuko ;
Kawasaki, Nana ;
Kawasaki, Nobuko ;
Kawasaki, Toshisuke .
JOURNAL OF LEUKOCYTE BIOLOGY, 2007, 81 (04) :1002-1011
[3]  
Benoist H, 2009, J LEUKOCYTE BIOL, V86, P103, DOI [10.1189/jlb.0708434, 10.1189/JLB.0708434]
[4]  
Castro AG, 1999, J IMMUNOL, V163, P5860
[5]   Activation of murine CD4+ and CD8+ T lymphocytes leads to dramatic remodeling of N-linked glycans [J].
Comelli, Elena M. ;
Sutton-Smith, Mark ;
Yan, Qi ;
Amado, Margarida ;
Panico, Maria ;
Gilmartin, Tim ;
Whisenant, Thomas ;
Lanigan, Caroline M. ;
Head, Steven R. ;
Goldberg, David ;
Morris, Howard R. ;
Dell, Anne ;
Paulson, James C. .
JOURNAL OF IMMUNOLOGY, 2006, 177 (04) :2431-2440
[6]   Temporal dynamics of CD69 expression on lymphoid cells [J].
Craston, R ;
Koh, M ;
Mc Dermott, A ;
Ray, N ;
Prentice, HG ;
Lowdell, MW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1997, 209 (01) :37-45
[7]   Diocleinae lectins are a group of proteins with conserved binding sites for the core trimannoside of asparagine-linked oligosaccharides and differential specificities for complex carbohydrates [J].
Dam, TK ;
Cavada, BS ;
Grangeiro, TB ;
Santos, CF ;
de Sousa, FAM ;
Oscarson, S ;
Brewer, CF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :12082-12088
[8]   Sweet 'n' sour: the impact of differential glycosylation on T cell responses [J].
Daniels, MA ;
Hogquist, KA ;
Jameson, SC .
NATURE IMMUNOLOGY, 2002, 3 (10) :903-910
[9]  
de Miranda-Santos I K, 1991, J Immunol Methods, V140, P197
[10]  
DEMIRANDASANTOS IKF, 1992, IMMUNOL LETT, V31, P65