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.
引用
收藏
页数:10
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