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白苋凝集素(ALL)增强抗-CD3 依赖性激活的小鼠 T 细胞,并促进细胞存活。

Amaranthus leucocarpus lectin (ALL) enhances anti-CD3-dependent activation of murine T cells and promotes cell survival.

机构信息

Departamento de Bioquímica, Instituto Nacional de Enfermedades Respiratorias Ismael CosioVillegas, Calzada de Tlalpan 4502, 14080, Mexico.

出版信息

Immunol Invest. 2011;40(2):113-29. doi: 10.3109/08820139.2010.503767. Epub 2010 Sep 1.

Abstract

The Galβ1,3GalNAc-specific lectin from Amaranthus leucocarpus (ALL) shows a differential binding pattern on murine thymocytes, peripheral and activated CD4(+) and CD8(+) 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(+) and CD8(+) 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.

摘要

来自苋属植物(Amaranthus leucocarpus)的 Galβ1,3GalNAc 特异性凝集素(ALL)在鼠胸腺细胞、外周和激活的 CD4(+)和 CD8(+)T 细胞上表现出不同的结合模式。尽管 ALL 检测到 T 细胞表面碳水化合物部分的激活相关变化,但尚未进行研究来检查 ALL 对 T 细胞激活的影响。在这项研究中,我们通过测量来自淋巴结的总细胞的增殖、表面激活标记物表达和 IL-2 分泌,分析了 ALL 存在下抗 CD3 依赖性的鼠 T 细胞激活。结果表明,ALL 不会显著诱导 T 细胞激活,但确实增强了 CD4(+)和 CD8(+)T 细胞的抗 CD3 依赖性激活。此外,ALL 可保护 T 细胞免受自发凋亡,并在无血清培养条件下增加细胞存活。我们的研究结果表明,ALL 本身不会影响 T 细胞激活,但表明 ALL 对 T 细胞激活具有抗 CD3 依赖性共刺激样作用。此外,ALL 促进常规和无血清培养条件下的细胞存活。这项研究首次报道了一种非有丝分裂 T 细胞结合凝集素,它可以诱导可能的共刺激样作用,并为理解糖基化如何影响 T 细胞反应提供了新的工具。

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