Characterization of TNF receptor subtype expression and signaling on pulmonary endothelial cells in mice

被引:22
作者
Bertok, Szabolcs [1 ]
Wilson, Michael R. [1 ]
Dorr, Anthony D. [1 ]
Dokpesi, Justina O. [1 ]
O'Dea, Kieran P. [1 ]
Marczin, Nandor [1 ]
Takata, Masao [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sect Anaesthet Pain Med & Intens Care, Chelsea & Westminster Hosp, Fac Med, London SW10 9NH, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
cytokine; adhesion molecule; inflammation; flow cytometry; lipopolysaccharide; TUMOR-NECROSIS-FACTOR; NF-KAPPA-B; FACTOR-ALPHA; SEPTIC SHOCK; MONOCLONAL-ANTIBODY; DOUBLE-BLIND; INFLAMMATORY CYTOKINES; PERSISTENT ELEVATION; FUNCTIONAL-ANALYSIS; EDEMA REABSORPTION;
D O I
10.1152/ajplung.00326.2010
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Bertok S, Wilson MR, Dorr AD, Dokpesi JO, O'Dea KP, Marczin N, Takata M. Characterization of TNF receptor subtype expression and signaling on pulmonary endothelial cells in mice. Am J Physiol Lung Cell Mol Physiol 300: L781-L789, 2011. First published March 4, 2011; doi:10.1152/ajplung.00326.2010.-TNF plays a crucial role in the pathogenesis of acute lung injury. However, the expression profile of its two receptors, p55 and p75, on pulmonary endothelium and their influence on TNF signaling during lung microvascular inflammation remain uncertain. Using flow cytometry, we characterized the expression profile of TNF receptors on the surface of freshly harvested pulmonary endothelial cells (PECs) from mice and found expression of both receptors with dominance of p55. To investigate the impact of stimulating individual TNF receptors, we treated wild-type and TNF receptor knockout mice with intravenous TNF and determined surface expression of adhesion molecules (E-selectin, VCAM-1, ICAM-1) on PECs by flow cytometry. TNF-induced upregulation of all adhesion molecules was substantially attenuated by absence of p55, whereas lack of p75 had a similar but smaller effect that varied between adhesion molecules. Selective blockade of individual TNF receptors by specific antibodies in wild-type primary PEC culture confirmed that the in vivo findings were due to direct effects of TNF receptor inhibition on endothelium and not other cells (e. g., circulating leukocytes). Finally, we found that PEC surface expression of p55 dramatically decreased in the early stages of endotoxemia following intravenous LPS, while no change in p75 expression was detected. These data demonstrate a crucial in vivo role of p55 and an auxiliary role of p75 in TNF-mediated adhesion molecule upregulation on PECs. It is possible that the importance of the individual receptors varies at different stages of pulmonary microvascular inflammation following changes in their relative expression.
引用
收藏
页码:L781 / L789
页数:9
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