Thromb Haemost 2004; 92(06): 1428-1437
DOI: 10.1160/TH04-06-0344
Endothelium and Vascular Development
Schattauer GmbH

Proinflammatory properties of murine aortic endothelial cells exclusively expressing a non cleavable form of TNFα

Effect on tumor necrosis factor α receptor type 2
Matthias Canault
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Franck Peiretti
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Christoph Mueller
1   Division of Immunopathology, Institute of Pathology, Bern, Switzerland
,
Paule Deprez
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Bernadette Bonardo
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Denis Bernot
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Irène Juhan-Vague
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
,
Gilles Nalbone
2   Inserm UMR-626, Faculté de Médecine, I.P.H.M., Marseille, France
› Institutsangaben
Financial support: This work was supported by funds of Inserm and Université de la Méditerranée. Matthias Canault is a funding recipient of Groupe d’Etude Hémostase et Thrombose (Paris).
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Publikationsverlauf

Received 04. Juni 2004

Accepted after resubmission 30. September 2004

Publikationsdatum:
04. Dezember 2017 (online)

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Summary

Soluble (sTNF) and transmembrane (tmTNF) forms of TNFα (TNF) have distinct proinflammatory effects. We investigated whether tmTNF altered the synthesis of some proinflammatory proteins involved in atherothrombosis, in murine aortas and aortic endothelial cells (MAEC). Samples were obtained from wild-type (WT) mice and TNF-deficient mice that express a mutated non cleavable tmTNF transgene (tmTNFnc).The levels of secreted MCP-1, RANTES, IL-6, PAI-1, soluble ICAM-1, and soluble TNF receptor type 1 (TNFR1; CD120a) antigens, MMP-9 activity and of cell surface ICAM-1 were not significantly different between the two types of MAEC.The magnitude of endotoxin-stimulated production of RANTES, MCP-1 and IL-6 was similar in the two types of cells. Of note, the amount of synthesized TNF receptor type 2 (TNFR2; CD120b), measured by its secreted (in aorta and MAEC), intracellular and mRNA levels (in MAEC), was significantly 4-fold lower in tmTNFnc than in WT mice, both in basal and endotoxin-stimulated conditions. A neutralizing anti-TNF antibody or the recombinant murine TNF did not modify the magnitude of the difference in TNFR2 production between the two types of cells, suggesting a preponderant role of tmTNF in the down-regulation of TNFR2 synthesis. Macrophages of tmTNFnc mice also produced less TNFR2 than WT macrophages (−30%). Plasmas of tmTNFnc mice contained significantly less sTNFR2 than WT mice (−75%). In conclusion, an increase in tmTNF levels, rather than the lack of sTNF, significantly down-modulated TNFR2 synthesis in aortic endothelial cells, but had no major influence on the synthesis of some major pro-inflammatory and pro-atherothrombotic proteins.