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Glycine inhibits NINJ1 membrane clustering to suppress plasma membrane rupture in cell death.
Borges, Jazlyn P; Sætra, Ragnhild S R; Volchuk, Allen; Bugge, Marit; Devant, Pascal; Sporsheim, Bjørnar; Kilburn, Bridget R; Evavold, Charles L; Kagan, Jonathan C; Goldenberg, Neil M; Flo, Trude Helen; Steinberg, Benjamin Ethan.
Afiliação
  • Borges JP; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Canada.
  • Sætra RSR; Centre of Molecular Inflammation Research, Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
  • Volchuk A; Program in Cell Biology, Hospital for Sick Children, Toronto, Canada.
  • Bugge M; Centre of Molecular Inflammation Research, Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
  • Devant P; Division of Gastroenterology, Boston Children's Hospital and Harvard Medical School, Boston, United States.
  • Sporsheim B; Centre of Molecular Inflammation Research, Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
  • Kilburn BR; Program in Neuroscience and Mental Health, Hospital for Sick Children, Toronto, Canada.
  • Evavold CL; Ragon Institute of MGH, MIT and Harvard, Boston, United States.
  • Kagan JC; Division of Gastroenterology, Boston Children's Hospital and Harvard Medical School, Boston, United States.
  • Goldenberg NM; Program in Cell Biology, Hospital for Sick Children, Toronto, Canada.
  • Flo TH; Department of Anesthesia and Pain Medicine, Hospital for Sick Children, Toronto, Canada.
  • Steinberg BE; Department of Anesthesiology and Pain Medicine, University of Toronto, Toronto, Canada.
Elife ; 112022 12 05.
Article em En | MEDLINE | ID: mdl-36468682
ABSTRACT
First recognized more than 30 years ago, glycine protects cells against rupture from diverse types of injury. This robust and widely observed effect has been speculated to target a late downstream process common to multiple modes of tissue injury. The molecular target of glycine that mediates cytoprotection, however, remains elusive. Here, we show that glycine works at the level of NINJ1, a newly identified executioner of plasma membrane rupture in pyroptosis, necrosis, and post-apoptosis lysis. NINJ1 is thought to cluster within the plasma membrane to cause cell rupture. We demonstrate that the execution of pyroptotic cell rupture is similar for human and mouse NINJ1 and that NINJ1 knockout functionally and morphologically phenocopies glycine cytoprotection in macrophages undergoing lytic cell death. Next, we show that glycine prevents NINJ1 clustering by either direct or indirect mechanisms. In pyroptosis, glycine preserves cellular integrity but does not affect upstream inflammasome activities or accompanying energetic cell death. By positioning NINJ1 clustering as a glycine target, our data resolve a long-standing mechanism for glycine-mediated cytoprotection. This new understanding will inform the development of cell preservation strategies to counter pathologic lytic cell death.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piroptose / Glicina Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piroptose / Glicina Limite: Animals / Humans Idioma: En Revista: Elife Ano de publicação: 2022 Tipo de documento: Article