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Emerging role of alpha2,6-sialic acid as a negative regulator of galectin binding and function.α2,6-唾液酸作为半乳糖凝集素结合和功能的负调节剂的新作用。
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N- and O-glycans modulate galectin-1 binding, CD45 signaling, and T cell death.N- 和 O-聚糖调节半乳糖凝集素-1 的结合、CD45 信号转导和 T 细胞死亡。
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本文引用的文献

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Impaired thymopoiesis in interleukin-7 receptor transgenic mice is not corrected by Bcl-2.白细胞介素-7受体转基因小鼠中受损的胸腺生成不能被Bcl-2纠正。
Cell Immunol. 2007 Nov-Dec;250(1-2):31-9. doi: 10.1016/j.cellimm.2008.01.002. Epub 2008 Mar 5.
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alpha 2-6-Linked sialic acids on N-glycans modulate carcinoma differentiation in vivo.N-聚糖上的α2-6连接唾液酸在体内调节癌分化。
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Involvement of Annexin A2 in p53 induced apoptosis in lung cancer.膜联蛋白A2在p53诱导的肺癌细胞凋亡中的作用
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The murine pan T cell marker CD96 is an adhesion receptor for CD155 and nectin-1.小鼠全T细胞标志物CD96是CD155和nectin-1的黏附受体。
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T cell lineage determination precedes the initiation of TCR beta gene rearrangement.T细胞谱系的确定先于TCRβ基因重排的起始。
J Immunol. 2007 Sep 15;179(6):3699-706. doi: 10.4049/jimmunol.179.6.3699.
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T-cell activation results in microheterogeneous changes in glycosylation of CD45.T细胞活化导致CD45糖基化的微异质性变化。
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Glycan-based interactions involving vertebrate sialic-acid-recognizing proteins.涉及脊椎动物唾液酸识别蛋白的基于聚糖的相互作用。
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Structural and mechanistic features of protein O glycosylation linked to CD8+ T-cell apoptosis.与CD8+ T细胞凋亡相关的蛋白质O-糖基化的结构和机制特征
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9
Attenuation of cytokine responsiveness during T cell development and differentiation.T细胞发育和分化过程中细胞因子反应性的减弱。
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Glycosylation in cellular mechanisms of health and disease.健康与疾病细胞机制中的糖基化作用。
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ST6Gal I基因缺陷小鼠中胸腺细胞生成的破坏。

Disruption of thymopoiesis in ST6Gal I-deficient mice.

作者信息

Marino Julie H, Tan Chibing, Davis Brenda, Han Eun-Soo, Hickey Morgan, Naukam Rebecca, Taylor Ashlee, Miller Kenton S, Van De Wiele C Justin, Teague T Kent

机构信息

Department of Surgery, University of Oklahoma College of Medicine, Tulsa, OK 74135, USA.

出版信息

Glycobiology. 2008 Sep;18(9):719-26. doi: 10.1093/glycob/cwn051. Epub 2008 Jun 5.

DOI:10.1093/glycob/cwn051
PMID:18535087
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2733770/
Abstract

Thymocyte development is accompanied by sequential changes in cell surface glycosylation. For example, medullary thymocytes have increased levels of alpha2,3-linked sialic acid and a loss of asialo core 1 O-glycans as compared to cortical thymocytes. Some of these changes have been linked to fine tuning of the T cell receptor avidity. We analyzed ST6Gal I transcript abundance and levels of alpha2,6-linked sialic acid across thymocyte subsets. We found that ST6Gal I transcript levels increased following T cell receptor beta-selection suggesting that this sialyltransferase may influence the development of early thymocyte populations. Indeed, low levels of alpha2,6-linked sialic acid were found in the earliest T lineage cells, and then increased in T cell receptor beta-selected cells. To determine whether ST6Gal I influences T cell development, we analyzed ST6Gal I-deficient mice for disruptions in thymocyte populations. We found reduced thymic cellularity in the ST6Gal I-deficient mice starting in the early thymocyte compartments.

摘要

胸腺细胞的发育伴随着细胞表面糖基化的一系列变化。例如,与皮质胸腺细胞相比,髓质胸腺细胞中α2,3连接的唾液酸水平增加,而脱唾液酸核心1 O-聚糖减少。其中一些变化与T细胞受体亲和力的微调有关。我们分析了跨胸腺细胞亚群的ST6Gal I转录本丰度和α2,6连接的唾液酸水平。我们发现,在T细胞受体β选择后,ST6Gal I转录本水平增加,这表明这种唾液酸转移酶可能影响早期胸腺细胞群体的发育。事实上,在最早的T系细胞中发现低水平的α2,6连接的唾液酸,然后在T细胞受体β选择的细胞中增加。为了确定ST6Gal I是否影响T细胞发育,我们分析了ST6Gal I缺陷小鼠的胸腺细胞群体是否受到破坏。我们发现,从早期胸腺细胞区室开始,ST6Gal I缺陷小鼠的胸腺细胞数量减少。