MLKL compromises plasma membrane integrity by binding to phosphatidylinositol phosphatesReportar como inadecuado

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(2014)CELL REPORTS.7(4).p.971-981 Mark abstract Although mixed lineage kinase domain-like (MLKL) protein has emerged as a specific and crucial protein for necroptosis induction, how MLKL transduces the death signal remains poorly understood. Here, we demonstrate that the full four-helical bundle domain (4HBD) in the N-terminal region of MLKL is required and sufficient to induce its oligomerization and trigger cell death. Moreover, we found that a patch of positively charged amino acids on the surface of the 4HBD binds to phosphatidylinositol phosphates (PIPs) and allows recruitment of MLKL to the plasma membrane. Importantly, we found that recombinant MLKL, but not a mutant lacking these positive charges, induces leakage of PIP-containing liposomes as potently as BAX, supporting a model in which MLKL induces necroptosis by directly permeabilizing the plasma membrane. Accordingly, we found that inhibiting the formation of PI(5) P and PI(4,5) P-2 specifically inhibits tumor necrosis factor (TNF)-mediated necroptosis but not apoptosis.

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Autor: Yves Dondelinger, Wim Declercq , Sylvie Montessuit, Ria Roelandt , Amanda Gonçalves , Inge Bruggeman , Paco Hulpiau , Kathrin Web



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