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CD95L concatemers highlight different stoichiometries of CD95-mediated apoptotic and nonapoptotic pathways.
Lebrault, Eden; Oblet, Christelle; Kurma, Keerthi; Levoin, Nicolas; Jeannet, Robin; Jean, Mickael; Vacher, Pierre; Legembre, Patrick.
Affiliation
  • Lebrault E; UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.
  • Oblet C; UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.
  • Kurma K; Laboratory of Rare Human Circulating Cells (LCCRH), University Medical Centre of Montpellier, Montpellier, France.
  • Levoin N; Bioprojet Biotech, Saint-Grégoire, France.
  • Jeannet R; UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.
  • Jean M; Institut des Sciences Chimiques de Rennes-UMR CNRS 6226 Equipe COrInt, Université de Rennes, Rennes, France.
  • Vacher P; INSERM, Centre de Recherche Cardio-Thoracique de Bordeaux, Pessac, France.
  • Legembre P; UMR CNRS 7276, INSERM U1262, CRIBL, Université Limoges, Limoges, France.
Eur J Immunol ; 54(1): e2350626, 2024 Jan.
Article in En | MEDLINE | ID: mdl-37837385
ABSTRACT
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)2 . These ligands reveal that although the hexameric structure is the best stoichiometry to trigger cell death, a dimer is sufficient to induce the apoptotic response in CD95-sensitive Jurkat cells. Interestingly, only trimeric and hexameric forms can implement a potent Ca2+ response, suggesting that while CD95 aggregation controls the implementation of the apoptotic signal, both aggregation and conformation are required to implement the Ca2+ pathway.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Fas Receptor Limits: Humans Language: En Journal: Eur J Immunol Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Apoptosis / Fas Receptor Limits: Humans Language: En Journal: Eur J Immunol Year: 2024 Document type: Article