NINJ1 mediates plasma membrane rupture by cutting and releasing membrane disks

Liron David, Jazlyn P. Borges, L. Robert Hollingsworth, Allen Volchuk, Isabelle Jansen, Evelyn Garlick, Benjamin E. Steinberg, Hao Wu

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

The membrane protein NINJ1 mediates plasma membrane rupture in pyroptosis and other lytic cell death pathways. Here, we report the cryo-EM structure of a NINJ1 oligomer segmented from NINJ1 rings. Each NINJ1 subunit comprises amphipathic (⍺1, ⍺2) and transmembrane (TM) helices (⍺3, ⍺4) and forms a chain of subunits, mainly by the TM helices and ⍺1. ⍺3 and ⍺4 are kinked, and the Gly residues are important for function. The NINJ1 oligomer possesses a concave hydrophobic side that should face the membrane and a convex hydrophilic side formed by ⍺1 and ⍺2, presumably upon activation. This structural observation suggests that NINJ1 can form membrane disks, consistent with membrane fragmentation by recombinant NINJ1. Live-cell and super-resolution imaging uncover ring-like structures on the plasma membrane that are released into the culture supernatant. Released NINJ1 encircles a membrane inside, as shown by lipid staining. Therefore, NINJ1-mediated membrane disk formation is different from gasdermin-mediated pore formation, resulting in membrane loss and plasma membrane rupture.

Original languageEnglish
Pages (from-to)2224-2235.e16
JournalCell
Volume187
Issue number9
DOIs
StatePublished - 25 Apr 2024
Externally publishedYes

Keywords

  • NINJ1
  • NINJ2
  • Ninjurin1
  • Ninjurin2
  • cryo-EM
  • inflammasome
  • inflammation
  • lytic cell death
  • plasma membrane rupture
  • pyroptosis

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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