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

77 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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