Abstract

IntroductionGrowth arrest-specific gene 6 protein (GAS6) and protein S (ProS) are vitamin K-dependent proteins present in plasma with important regulatory functions in systems of response and repair to damage. They interact with receptor tyrosine kinases of the Tyro3, Axl and MerTK receptor tyrosine kinase (TAM) family, involved in apoptotic cell clearance (efferocytosis) and regulation of the innate immunity. TAM-deficient mice show spontaneous lupus-like symptoms. Here we tested the genetic profile and plasma levels of components of the system in patients with systemic lupus erythematosus (SLE), and compare them with a control healthy population.MethodsFifty SLE patients and 50 healthy controls with matched age, gender and from the same geographic area were compared. Genetic analysis was performed in GAS6 and the TAM receptor genes on SNPs previously identified. The concentrations of GAS6, total and free ProS, and the soluble forms of the three TAM receptors (sAxl, sMerTK and sTyro3) were measured in plasma from these samples.ResultsPlasma concentrations of GAS6 were higher and, total and free ProS were lower in the SLE patients compared to controls, even when patients on oral anticoagulant treatment were discarded. Those parameters correlated with SLE disease activity index (SLEDAI) score, GAS6 being higher in the most severe cases, while free and total ProS were lower. All 3 soluble receptors increased its concentration in plasma of lupus patients.ConclusionsThe present study highlights that the GAS6/ProS-TAM system correlates in several ways with disease activity in SLE. We show here that this correlation is affected by common polymorphisms in the genes of the system. These findings underscore the importance of mechanism of regulatory control of innate immunity in the pathology of SLE.

Highlights

  • Growth arrest-specific gene 6 protein (GAS6) and protein S (ProS) are vitamin K-dependent proteins present in plasma with important regulatory functions in systems of response and repair to damage

  • Those parameters correlated with systemic lupus erythematosus (SLE) disease activity index (SLEDAI) score, growth arrest-specific 6 (GAS6) being higher in the most severe cases, while free and total ProS were lower

  • The present study highlights that the GAS6/ProS-TAM system correlates in several ways with disease activity in SLE

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Summary

Introduction

Growth arrest-specific gene 6 protein (GAS6) and protein S (ProS) are vitamin K-dependent proteins present in plasma with important regulatory functions in systems of response and repair to damage. They interact with receptor tyrosine kinases of the Tyro, Axl and MerTK receptor tyrosine kinase (TAM) family, involved in apoptotic cell clearance (efferocytosis) and regulation of the innate immunity. Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by an impairment of the regulation of the immune system [1] This is reflected in hyperactivity of lymphocytes, the production of pathogenic auto-antibodies, and the formation of immune complexes, which can lead to multi-organ damage. The main ligands that bind to and activate the TAM family of receptors are growth arrest-specific 6 (GAS6) and protein S (ProS), which are capable of binding to negatively charged residues exposed early in apoptosis on the membrane surface of the apoptotic cell [9]

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