共 8 条
Reinforcement of integrin-mediated T-Lymphocyte adhesion by TNF-induced Inside-out Signaling
被引:8
作者:
Li, Qian
[1
,3
]
Huth, Steven
[1
]
Adam, Dieter
[2
]
Selhuber-Unkel, Christine
[1
]
机构:
[1] Univ Kiel, Biocompatible Nanomat, Inst Mat Sci, Kaiserstr 2, D-24143 Kiel, Germany
[2] Univ Kiel, Inst Immunol, Michaelisstr 5, D-24105 Kiel, Germany
[3] Chinese Acad Sci, High Field Magnet Lab, Hefei 230031, Anhui, Peoples R China
来源:
SCIENTIFIC REPORTS
|
2016年
/
6卷
基金:
欧洲研究理事会;
关键词:
WD-REPEAT PROTEIN;
CELL-ADHESION;
RECEPTOR;
FIBRONECTIN;
ACTIVATION;
BONDS;
MODULATION;
MOLECULE-1;
INDUCTION;
INTERACTS;
D O I:
10.1038/srep30452
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Integrin-mediated leukocyte adhesion to endothelial cells is a crucial step in immunity against pathogens. Whereas the outside-in signaling pathway in response to the pro-inflammatory cytokine tumour necrosis factor (TNF) has already been studied in detail, little knowledge exists about a supposed TNF-mediated inside-out signaling pathway. In contrast to the outside-in signaling pathway, which relies on the TNF-induced upregulation of surface molecules on endothelium, inside-out signaling should also be present in an endothelium-free environment. Using single-cell force spectroscopy, we show here that stimulating Jurkat cells with TNF significantly reinforces their adhesion to fibronectin in a biomimetic in vitro assay for cell-surface contact times of about 1.5 seconds, whereas for larger contact times the effect disappears. Analysis of single-molecule ruptures further demonstrates that TNF strengthens sub-cellular single rupture events at short cell-surface contact times. Hence, our results provide quantitative evidence for the significant impact of TNF-induced inside-out signaling in the T-lymphocyte initial adhesion machinery.
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页数:10
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