ZMPSTE24 defends against influenza and other pathogenic viruses

J Exp Med. 2017 Apr 3;214(4):919-929. doi: 10.1084/jem.20161270. Epub 2017 Feb 28.

Abstract

Zinc metallopeptidase STE24 (ZMPSTE24) is a transmembrane metalloprotease whose catalytic activity is critical for processing lamin A on the inner nuclear membrane and clearing clogged translocons on the endoplasmic reticulum. We now report ZMPSTE24 is a virus-specific effector that restricts enveloped RNA and DNA viruses, including influenza A, Zika, Ebola, Sindbis, vesicular stomatitis, cowpox, and vaccinia, but not murine leukemia or adenovirus. ZMPSTE24-mediated antiviral action is independent of protease activity. Coimmunoprecipitation studies indicate ZMPSTE24 can complex with proteins of the interferon-induced transmembrane protein (IFITM) family. IFITM proteins impede viral entry, and ZMPSTE24 expression is necessary for IFITM antiviral activity. In vivo studies demonstrate ZMPSTE24-deficient mice display higher viral burdens, enhanced cytokine production, and increased mortality after influenza infection. Collectively, these findings identify ZMPSTE24 as an intrinsic broad-spectrum antiviral protein and provide insights into antiviral defense mechanisms.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / physiology
  • Cytokines / biosynthesis
  • HEK293 Cells
  • Humans
  • Influenza, Human / prevention & control*
  • Membrane Proteins / physiology*
  • Metalloendopeptidases / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Virus Diseases / prevention & control*

Substances

  • Antigens, Differentiation
  • Cytokines
  • Membrane Proteins
  • leu-13 antigen
  • Metalloendopeptidases
  • Zmpste24 protein, mouse
  • ZMPSTE24 protein, human