To Kill But Not Be Killed: Controlling the Activity of Mammalian Pore-Forming Proteins

Front Immunol. 2020 Nov 13:11:601405. doi: 10.3389/fimmu.2020.601405. eCollection 2020.

Abstract

Pore-forming proteins (PFPs) are present in all domains of life, and play an important role in host-pathogen warfare and in the elimination of cancers. They can be employed to deliver specific effectors across membranes, to disrupt membrane integrity interfering with cell homeostasis, and to lyse membranes either destroying intracellular organelles or entire cells. Considering the destructive potential of PFPs, it is perhaps not surprising that mechanisms controlling their activity are remarkably complex, especially in multicellular organisms. Mammalian PFPs discovered to date include the complement membrane attack complex (MAC), perforins, as well as gasdermins. While the primary function of perforin-1 and gasdermins is to eliminate infected or cancerous host cells, perforin-2 and MAC can target pathogens directly. Yet, all mammalian PFPs are in principle capable of generating pores in membranes of healthy host cells which-if uncontrolled-could have dire, and potentially lethal consequences. In this review, we will highlight the strategies employed to protect the host from destruction by endogenous PFPs, while enabling timely and efficient elimination of target cells.

Keywords: gasdermins; immunity; membrane attack complex; membrane integrity; perforins; pore-forming proteins.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptive Immunity
  • Animals
  • Complement Membrane Attack Complex / metabolism
  • Cytotoxicity, Immunologic*
  • Humans
  • Immune System / immunology
  • Immune System / metabolism*
  • Immunity, Innate
  • Perforin / metabolism
  • Pore Forming Cytotoxic Proteins / genetics
  • Pore Forming Cytotoxic Proteins / metabolism*
  • Signal Transduction
  • Transcription, Genetic

Substances

  • Complement Membrane Attack Complex
  • Pore Forming Cytotoxic Proteins
  • Perforin