共 17 条
Comparative analysis of T-cell costimulation and CD43 activation reveals novel signaling pathways and target genes
被引:22
作者:

Mattioli, I
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机构: Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland

Dittrich-Breiholz, O
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h-index: 0
机构: Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland

Livingstone, M
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机构: Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland

Kracht, M
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h-index: 0
机构: Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland

Schmitz, ML
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h-index: 0
机构: Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
机构:
[1] Univ Bern, Dept Chem & Biochem, CH-3012 Bern, Switzerland
[2] Cell Signaling Technol, Beverly, MA USA
[3] Hannover Med Sch, Inst Pharmacol, D-3000 Hannover, Germany
来源:
关键词:
D O I:
10.1182/blood-2004-04-1536
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The CD43 lymphocyte surface receptor is involved in the regulation of lymphocyte adhesion and activation. Many CD43 functions remain controversial or unclear, and it is not known to which extent CD43 signaling pathways are shared with or distinct from those used by the T-cell receptor (TCR). Here, we systematically compared signaling events and target gene expression induced by CD43 or T-cell costimulation in primary human peripheral T cells. These studies identify nuclear factor-kappaB (NF-kappaB) p65 serine 468 as a novel inducible phosphorylation site strongly induced by T-cell costimulation and only weakly triggered by CD43 ligation. We also identified CD43 as a novel Jun N-terminal kinase (JNK) activator and a comprehensive analysis of further Signaling events suggests that both stimuli use overlapping but also distinct signaling pathways. Microarray analysis of inflammatory genes shows 1 group of genes coregulated by both stimuli and 2 further groups of target genes affected solely by costimulation or primarily by CD43. (C) 2004 by The American Society of Hematology.
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页码:3302 / 3304
页数:3
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