Could Gas6/TAM Axis Provide Valuable Insights into the Pathogenesis of Systemic Sclerosis?

Author:

Apostolo Daria12ORCID,D’Onghia Davide1ORCID,Nerviani Alessandra2ORCID,Ghirardi Giulia Maria2,Sola Daniele13ORCID,Perazzi Mattia14,Tonello Stelvio1ORCID,Colangelo Donato5ORCID,Sainaghi Pier Paolo146ORCID,Bellan Mattia146ORCID

Affiliation:

1. Department of Translational Medicine, University of Piemonte Orientale (UPO), 28100 Novara, Italy

2. Centre for Experimental Medicine and Rheumatology, Barts and The London School of Medicine and Dentistry, William Harvey Research Institute, Queen Mary University of London, London E1 4NS, UK

3. IRCCS Istituto Auxologico Italiano, UO General Medicine, 28824 Oggebbio, Italy

4. Internal Medicine and Rheumatology Unit, A.O.U. Maggiore della Carità, 28100 Novara, Italy

5. Department of Health Sciences, Pharmacology, University of Piemonte Orientale (UPO), 28100 Novara, Italy

6. Center on Autoimmune and Allergic Diseases (CAAD), University of Piemonte Orientale, 28100 Novara, Italy

Abstract

Systemic sclerosis (SSc) is a connective tissue disorder characterized by microvascular injury, extracellular matrix deposition, autoimmunity, inflammation, and fibrosis. The clinical complexity and high heterogeneity of the disease make the discovery of potential therapeutic targets difficult. However, the recent progress in the comprehension of its pathogenesis is encouraging. Growth Arrest-Specific 6 (Gas6) and Tyro3, Axl, and MerTK (TAM) receptors are involved in multiple biological processes, including modulation of the immune response, phagocytosis, apoptosis, fibrosis, inflammation, cancer development, and autoimmune disorders. In the present manuscript, we review the current evidence regarding SSc pathogenesis and the role of the Gas6/TAM system in several human diseases, suggesting its likely contribution in SSc and highlighting areas where further research is necessary to fully comprehend the role of TAM receptors in this condition. Indeed, understanding the involvement of TAM receptors in SSc, which is currently unknown, could provide valuable insights for novel potential therapeutic targets.

Publisher

MDPI AG

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