Gas6/TAM Axis Involvement in Modulating Inflammation and Fibrosis in COVID-19 Patients

Int J Mol Sci. 2023 Jan 4;24(2):951. doi: 10.3390/ijms24020951.

Abstract

Gas6 (growth arrest-specific gene 6) is a widely expressed vitamin K-dependent protein that is involved in many biological processes such as homeostatic regulation, inflammation and repair/fibrotic processes. It is known that it is the main ligand of TAMs, a tyrosine kinase receptor family of three members, namely MerTK, Tyro-3 and Axl, for which it displays the highest affinity. Gas6/TAM axis activation is known to be involved in modulating inflammatory responses as well as fibrotic evolution in many different pathological conditions. Due to the rapidly evolving COVID-19 pandemic, this review will focus on Gas6/TAM axis activation in SARS-CoV-2 infection, where de-regulated inflammatory responses and fibrosis represent a relevant feature of severe disease manifestation. Furthermore, this review will highlight the most recent scientific evidence supporting an unsuspected role of Axl as a SARS-CoV-2 infection driver, and the potential therapeutic advantages of the use of existing Axl inhibitors in COVID-19 management. From a physiological point of view, the Gas6/TAM axis plays a dual role, fostering the tissue repair processes or leading to organ damage and loss of function, depending on the prevalence of its anti-inflammatory or profibrotic properties. This review makes a strong case for further research focusing on the Gas6/TAM axis as a pharmacological target to manage different disease conditions, such as chronic fibrosis or COVID-19.

Keywords: COVID-19; Gas6; TAM receptors; fibrosis; inflammation.

Publication types

  • Review

MeSH terms

  • COVID-19*
  • Fibrosis
  • Humans
  • Inflammation
  • Pandemics*
  • SARS-CoV-2 / metabolism
  • c-Mer Tyrosine Kinase / genetics
  • c-Mer Tyrosine Kinase / metabolism

Substances

  • c-Mer Tyrosine Kinase

Supplementary concepts

  • Myeloproliferative Syndrome, Transient

Grants and funding

This research received no external funding.