A Review: The Potential Involvement of Growth Arrest-Specific 6 and Its Receptors in the Pathogenesis of Lung Damage and in Coronavirus Disease 2019.
Daria ApostoloLuciana L FerreiraAlice Di TizioBarbara RuaroFilippo PatruccoMattia BellanPublished in: Microorganisms (2023)
The tyrosine kinase receptors of the TAM family-Tyro3, Axl and Mer-and their main ligand Gas6 (growth arrest-specific 6) have been implicated in several human diseases, having a particularly important role in the regulation of innate immunity and inflammatory response. The Gas6/TAM system is involved in the recognition of apoptotic debris by immune cells and this mechanism has been exploited by viruses for cell entry and infection. Coronavirus disease 2019 (COVID-19) is a multi-systemic disease, but the lungs are particularly affected during the acute phase and some patients may suffer persistent lung damage. Among the manifestations of the disease, fibrotic abnormalities have been observed among the survivors of COVID-19. The mechanisms of COVID-related fibrosis remain elusive, even though some parallels may be drawn with other fibrotic diseases, such as idiopathic pulmonary fibrosis. Due to the still limited number of scientific studies addressing this question, in this review we aimed to integrate the current knowledge of the Gas6/TAM axis with the pathophysiological mechanisms underlying COVID-19, with emphasis on the development of a fibrotic phenotype.
Keyphrases
- coronavirus disease
- idiopathic pulmonary fibrosis
- tyrosine kinase
- inflammatory response
- respiratory syndrome coronavirus
- sars cov
- systemic sclerosis
- end stage renal disease
- interstitial lung disease
- endothelial cells
- epidermal growth factor receptor
- room temperature
- oxidative stress
- healthcare
- ejection fraction
- newly diagnosed
- cell death
- chronic kidney disease
- peritoneal dialysis
- young adults
- single cell
- stem cells
- prognostic factors
- cell therapy
- carbon dioxide
- lps induced
- anti inflammatory
- pluripotent stem cells
- ionic liquid