CD95L concatemers highlight different stoichiometries of CD95-mediated apoptotic and nonapoptotic pathways.

Apoptosis Calcium Concatemer Stoichiometry TNF

Journal

European journal of immunology
ISSN: 1521-4141
Titre abrégé: Eur J Immunol
Pays: Germany
ID NLM: 1273201

Informations de publication

Date de publication:
14 Oct 2023
Historique:
revised: 12 10 2023
received: 23 06 2023
accepted: 13 10 2023
pubmed: 15 10 2023
medline: 15 10 2023
entrez: 14 10 2023
Statut: aheadofprint

Résumé

To better understand the stoichiometry of CD95L required to trigger apoptotic and nonapoptotic signals, we generated several CD95L concatemers from dimer to hexamer conjugated via a flexible link (GGGGS)

Identifiants

pubmed: 37837385
doi: 10.1002/eji.202350626
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2350626

Subventions

Organisme : INCa PLBIO
ID : PLBIO 2018-132
Organisme : ANR
ID : ANR-22-CE15-0038-02
Organisme : ANR
ID : PCSI 2021 (CD95L-ProbInnov)
Organisme : Fondation de France
ID : Price Jean Valade
Organisme : PCSI
Organisme : Institut National Du Cancer
ID : PLBIO 2018-132

Informations de copyright

© 2023 The Authors. European Journal of Immunology published by Wiley-VCH GmbH.

Références

Strasser, A., Jost, P. J. and Nagata, S., The many roles of FAS receptor signaling in the immune system. Immunity 2009. 30: 180-192.
Levoin, N., Jean, M. and Legembre, P., CD95 structure, aggregation and cell signaling. Front. Cell Dev. Biol. 2020. 8: 314.
Schneider, P., Holler, N., Bodmer, J. L., Hahne, M., Frei, K., Fontana, A. and Tschopp, J., Conversion of membrane-bound Fas(CD95) ligand to its soluble form is associated with downregulation of its proapoptotic activity and loss of liver toxicity. J. Exp. Med. 1998. 187: 1205-1213.
Tauzin, S., Chaigne-Delalande, B., Selva, E., Khadra, N., Daburon, S., Contin-Bordes, C., Blanco, P. et al., The naturally processed CD95L elicits a c-yes/calcium/PI3K-driven cell migration pathway. PLoS Biol. 2011. 9: e1001090.
Chinnaiyan, A. M., O'Rourke, K., Tewari, M. and Dixit, V. M., FADD, a novel death domain-containing protein, interacts with the death domain of Fas and initiates apoptosis. Cell 1995. 81: 505-512.
Kischkel, F. C., Hellbardt, S., Behrmann, I., Germer, M., Pawlita, M., Krammer, P. H. and Peter, M. E., Cytotoxicity-dependent APO-1 (Fas/CD95)-associated proteins form a death-inducing signaling complex (DISC) with the receptor. Embo J. 1995. 14: 5579-5588.
Chinnaiyan, A. M., Tepper, C. G., Seldin, M. F., O'Rourke, K., Kischkel, F. C., Hellbardt, S., Krammer, P. H. et al., FADD/MORT1 is a common mediator of CD95 (Fas/APO-1) and tumor necrosis factor receptor-induced apoptosis. J. Biol. Chem. 1996. 271: 4961-4965.
Steller, E. J., Ritsma, L., Raats, D. A., Hoogwater, F. J., Emmink, B. L., Govaert, K. M., Laoukili, J. et al., The death receptor CD95 activates the cofilin pathway to stimulate tumour cell invasion. EMBO Rep. 2011. 12: 931-937.
Emrich, S. M., Yoast, R. E. and Trebak, M., Physiological functions of CRAC channels. Annu. Rev. Physiol. 2022. 84: 355-379.
Holler, N., Tardivel, A., Kovacsovics-Bankowski, M., Hertig, S., Gaide, O., Tinel, A., Deperthes, D. et al., Two adjacent trimeric Fas ligands are required for Fas signaling and formation of a death-inducing signaling complex. Mol. Cell. Biol. 2003. 23: 1428-1440.
Poissonnier, A., Sanseau, D., Le Gallo, M., Malleter, M., Levoin, N., Viel, R., Morere, L. et al., CD95-mediated calcium signaling promotes T helper 17 trafficking to inflamed organs in lupus-prone mice. Immunity 2016. 45: 209-223.
Herrero, R., Kajikawa, O., Matute-Bello, G., Wang, Y., Hagimoto, N., Mongovin, S., Wong, V. et al., The biological activity of FasL in human and mouse lungs is determined by the structure of its stalk region. J. Clin. Invest. 2011. 121: 1174-1190.
Devel, L., Guedeney, N., Bregant, S., Chowdhury, A., Jean, M. and Legembre, P., Role of metalloproteases in the CD95 signaling pathways. Front. Immunol. 2022. 13: 1074099.
Lavrik, I. N., Golks, A., Riess, D., Bentele, M., Eils, R. and Krammer, P. H., Analysis of CD95 threshold signaling: triggering of CD95 (FAS/APO-1) at low concentrations primarily results in survival signaling. J. Biol. Chem. 2007. 282: 13664-13671.
Legembre, P., Barnhart, B. C., Zheng, L., Vijayan, S., Straus, S. E., Puck, J., Dale, J. K. et al., Induction of apoptosis and activation of NF-kappaB by CD95 require different signalling thresholds. EMBO Rep. 2004. 5: 1084-1089.
Lang, I., Fick, A., Schafer, V., Giner, T., Siegmund, D. and Wajant, H., Signaling active CD95 receptor molecules trigger co-translocation of inactive CD95 molecules into lipid rafts. J. Biol. Chem. 2012. 287: 24026-24042.
Berg, D., Lehne, M., Muller, N., Siegmund, D., Munkel, S., Sebald, W., Pfizenmaier, K. et al., Enforced covalent trimerization increases the activity of the TNF ligand family members TRAIL and CD95L. Cell Death Differ. 2007. 14: 2021-2034.
Schneider, P., Bodmer, J. L., Holler, N., Mattmann, C., Scuderi, P., Terskikh, A., Peitsch, M. C. et al., Characterization of Fas (Apo-1, CD95)-Fas ligand interaction. J. Biol. Chem. 1997. 272: 18827-18833.
Liu, W., Ramagopal, U., Cheng, H., Bonanno, J. B., Toro, R., Bhosle, R., Zhan, C. et al., Crystal structure of the complex of human FasL and its decoy receptor DcR3. Structure 2016. 24: 2016-2023.
Kajikawa, O., Herrero, R., Chow, Y. H., Hung, C. F. and Matute-Bello, G., The bioactivity of soluble Fas ligand is modulated by key amino acids of its stalk region. PLoS One 2021. 16: e0253260.
Malleter, M., Tauzin, S., Bessede, A., Castellano, R., Goubard, A., Godey, F., Leveque, J. et al., CD95L cell surface cleavage triggers a prometastatic signaling pathway in triple-negative breast cancer. Cancer Res. 2013. 73: 6711-6721.
Poissonnier, A., Guegan, J. P., Nguyen, H. T., Best, D., Levoin, N., Kozlov, G., Gehring, K. et al., Disrupting the CD95-PLCgamma1 interaction prevents Th17-driven inflammation. Nat. Chem. Biol. 2018. 14: 1079-1089.
Vargo-Gogola, T., Crawford, H. C., Fingleton, B. and Matrisian, L. M., Identification of novel matrix metalloproteinase-7 (matrilysin) cleavage sites in murine and human Fas ligand. Arch. Biochem. Biophys. 2002. 408: 155-161.
Tanaka, M., Suda, T., Haze, K., Nakamura, N., Sato, K., Kimura, F., Motoyoshi, K. et al., Fas ligand in human serum. Nat. Med. 1996. 2: 317-322.
Suda, T., Hashimoto, H., Tanaka, M., Ochi, T. and Nagata, S., Membrane Fas ligand kills human peripheral blood T lymphocytes, and soluble Fas ligand blocks the killing. J. Exp. Med. 1997. 186: 2045-2050.

Auteurs

Eden Lebrault (E)

UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.

Christelle Oblet (C)

UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.

Keerthi Kurma (K)

Laboratory of Rare Human Circulating Cells (LCCRH), University Medical Centre of Montpellier, Montpellier, France.

Nicolas Levoin (N)

Bioprojet Biotech, Saint-Grégoire, France.

Robin Jeannet (R)

UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.

Mickael Jean (M)

Institut des Sciences Chimiques de Rennes-UMR CNRS 6226 Equipe COrInt, Université de Rennes, Rennes, France.

Pierre Vacher (P)

INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, Pessac, France.

Patrick Legembre (P)

UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.

Classifications MeSH