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Stress-induced sphingolipid signaling: role of type-2 neutral sphingomyelinase in murine cell apoptosis and proliferation.
Devillard R., Galvani S., Thiers J.-C., Guenet J.-L., Hannun Y. A., Bielawski J., Nègre-Salvayre A., Salvayre R., Augé N.
PLoS ONE 5, 3 (2010) e9826 - http://www.hal.inserm.fr/inserm-00504792
(20352118)
Stress-induced sphingolipid signaling: role of type-2 neutral sphingomyelinase in murine cell apoptosis and proliferation.
Raphael Devillard1, 2, Sylvain Galvani1, Jean-Claude Thiers1, Jean-Louis Guenet3, Yusuf Hannun4, Jacek Bielawski4, Anne Nègre-Salvayre1, Robert Salvayre1, Nathalie Augé () 1
1 :  I2MR - Institut de médecine moléculaire de Rangueil
INSERM : U858 – IFR31 – IFR150 – Université Paul Sabatier [UPS] - Toulouse III
Institut Louis Bugnard 1, avenue Jean Poulhes BP 84225 31432 TOULOUSE CEDEX 4
France
2 :  U.F.R d'Odontologie
Université Victor Segalen - Bordeaux II
146 rue Léo-Saignat - 33076 Bordeaux Cedex
France
3 :  Génétique des Mammifères
Institut Pasteur de Paris
25-28 rue du Dr Roux 75724 Paris
France
4 :  Department of Biochemistry and Molecular Biology
Medical University of South Carolina
Charleston, South Carolina
États-Unis
BACKGROUND: Sphingomyelin hydrolysis in response to stress-inducing agents, and subsequent ceramide generation, are implicated in various cellular responses, including apoptosis, inflammation and proliferation, depending on the nature of the different acidic or neutral sphingomyelinases. This study was carried out to investigate whether the neutral Mg(2+)-dependent neutral sphingomyelinase-2 (nSMase2) plays a role in the cellular signaling evoked by TNFalpha and oxidized LDLs, two stress-inducing agents, which are mitogenic at low concentrations and proapoptotic at higher concentrations. METHODOLOGY AND PRINCIPAL FINDINGS: For this purpose, we used nSMase2-deficient cells from homozygous fro/fro (fragilitas ossium) mice and nSMase2-deficient cells reconstituted with a V5-tagged nSMase2. We report that the genetic defect of nSMase2 (in fibroblasts from fro/fro mice) does not alter the TNFalpha and oxidized LDLs-mediated apoptotic response. Likewise, the hepatic toxicity of TNFalpha is similar in wild type and fro mice, thus is independent of nSMase2 activation. In contrast, the mitogenic response elicited by low concentrations of TNFalpha and oxidized LDLs (but not fetal calf serum) requires nSMase2 activation. CONCLUSION AND SIGNIFICANCE: nSMase2 activation is not involved in apoptosis mediated by TNFalpha and oxidized LDLs in murine fibroblasts, and in the hepatotoxicity of TNFalpha in mice, but is required for the mitogenic response to stress-inducing agents.
Sciences du Vivant/Biologie cellulaire
Anglais
1932-6203

Articles dans des revues avec comité de lecture
10.1371/journal.pone.0009826
PLoS ONE
Publisher Public Library of Science
ISSN 1932-6203 
internationale
2010
23/03/2010
5
3
e9826

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journal.pone.0009826.pdf(3.6 MB)