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前沿:Th1细胞中负责选择素配体形成的糖基转移酶表达对Stat4的不同需求。

Cutting edge: differential requirements for Stat4 in expression of glycosyltransferases responsible for selectin ligand formation in Th1 cells.

作者信息

White S J, Underhill G H, Kaplan M H, Kansas G S

机构信息

Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, IL 60611, USA.

出版信息

J Immunol. 2001 Jul 15;167(2):628-31. doi: 10.4049/jimmunol.167.2.628.

Abstract

A role for Stat4 in IL-12-induced up-regulation of selectin ligands on Th1 cells was explored. Th1 cells generated from Stat4(-/-) mice exhibited no IL-12-inducible P-selectin ligands, no up-regulation of core 2 beta1,6-glucosaminyltransferase I (C2GlcNAcT-I), and low levels of the Th1 transcription factor T-bet. In contrast, Stat4(-/-) Th1 cells exhibited only a partial defect in expression of IL-12-inducible E-selectin ligands and expressed equivalently high levels of alpha1,3-fucosyltransferase VII (FucT-VII) as wild-type Th1 cells. FucT-VII expression was induced by T cell activation, and was enhanced by IL-12 independently of Stat4, whereas C2GlcNAcT-I up-regulation was mediated exclusively by IL-12, acting through Stat4. These data show that FucT-VII and C2GlcNAcT-I are controlled through distinct pathways and imply the existence of at least one other IL-12-inducible glycosyltransferase required for E-selectin and possibly P-selectin ligand formation in Th1 cells.

摘要

研究了Stat4在白细胞介素-12(IL-12)诱导的Th1细胞上选择素配体上调中的作用。来自Stat4基因敲除小鼠的Th1细胞未表现出IL-12诱导的P选择素配体,核心2β1,6-氨基葡萄糖基转移酶I(C2GlcNAcT-I)未上调,且Th1转录因子T-bet水平较低。相比之下,Stat4基因敲除的Th1细胞在IL-12诱导的E选择素配体表达方面仅表现出部分缺陷,并且与野生型Th1细胞一样表达高水平的α1,3-岩藻糖基转移酶VII(FucT-VII)。FucT-VII的表达由T细胞激活诱导,并且IL-12可独立于Stat4增强其表达,而C2GlcNAcT-I的上调仅由通过Stat4起作用的IL-12介导。这些数据表明FucT-VII和C2GlcNAcT-I通过不同途径受到调控,并暗示在Th1细胞中存在至少一种其他IL-12诱导的糖基转移酶,它是E选择素以及可能的P选择素配体形成所必需的。

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