β-arrestins and G protein-coupled receptor kinases in viral entry: A graphical review

Cell Signal. 2023 Feb:102:110558. doi: 10.1016/j.cellsig.2022.110558. Epub 2022 Dec 9.

Abstract

Viruses rely on host-cell machinery in order to invade host cells and carry out a successful infection. G-protein coupled receptor (GPCR)-mediated signaling pathways are master regulators of cellular physiological processing and are an attractive target for viruses to rewire cells during infection. In particular, the GPCR-associated scaffolding proteins β-arrestins and GPCR signaling effectors G-protein receptor kinases (GRKs) have been identified as key cellular factors that mediate viral entry and orchestrate signaling pathways that reprogram cells for viral replication. Interestingly, a broad range of viruses have been identified to activate and/or require GPCR-mediated pathways for infection, including polyomaviruses, flaviviruses, influenza virus, and SARS-CoV-2, demonstrating that these viruses may have conserved mechanisms of host-cell invasion. Thus, GPCR-mediated pathways highlight an attractive target for the development of broad antiviral therapies.

Keywords: B-arrestin; Clathrin; Endocytosis; Filovirus; Flavivirus; G protein; GPCR; GRK; Influenza virus; Polyomavirus; Signaling; Virus.

Publication types

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

MeSH terms

  • COVID-19*
  • G-Protein-Coupled Receptor Kinases* / metabolism
  • Humans
  • Phosphorylation
  • Receptors, G-Protein-Coupled / metabolism
  • SARS-CoV-2
  • Virus Internalization
  • beta-Arrestins / metabolism

Substances

  • G-Protein-Coupled Receptor Kinases
  • beta-Arrestins
  • Receptors, G-Protein-Coupled