Elevated Plasma Levels of Growth Arrest Specific 6 (Gas6) Protein in Severe Obesity: Implications for Adipose Tissue and Inflammation.


Journal

Medical science monitor : international medical journal of experimental and clinical research
ISSN: 1643-3750
Titre abrégé: Med Sci Monit
Pays: United States
ID NLM: 9609063

Informations de publication

Date de publication:
27 Jun 2024
Historique:
medline: 27 6 2024
pubmed: 27 6 2024
entrez: 27 6 2024
Statut: epublish

Résumé

BACKGROUND Preliminary data suggest an adipogenic role for growth arrest-specific 6 (Gas6), a pleiotropic molecule involved in inflammation, proliferation, and hemostasis through its Tyro3, Axl, and MerTK (TAM) receptors. This study compares Gas6 expression in plasma and visceral and subcutaneous adipose tissue in 42 adults with obesity (body mass index ≥40 kg/m²) and 32 normal-weight controls to elucidate its role in obesity and related metabolic alterations. MATERIAL AND METHODS Using a case-control design, we measured Gas6 levels in plasma via a validated sandwich enzyme-linked immunosorbent assay and in adipose tissues through quantitative polymerase chain reactio with specific probes. Medians and correlations were analyzed using Mann-Whitney and Spearman tests. A general linear model assessed the impact of covariates on the Gas6-anthropometric relationship, with statistical significance determined by P values. RESULTS Plasma Gas6 levels were significantly higher in the obese group than in controls (P=0.0006). While Gas6 mRNA expression did not significantly differ in subcutaneous adipose tissue between groups, it was notably higher in visceral than subcutaneous adipose tissue in controls (P<0.05). A significant correlation was found between plasma Gas6 levels and body mass index (P=0.001). CONCLUSIONS Gas6 plasma levels are elevated in morbid obesity, particularly in visceral adipose tissue, and are linked to altered glucose tolerance in female patients. These findings highlight the role of Gas6 in obesity-related metabolic complications and suggest avenues for further research and potential therapies.

Identifiants

pubmed: 38932442
pii: 944462
doi: 10.12659/MSM.944462
doi:

Substances chimiques

growth arrest-specific protein 6 0
Intercellular Signaling Peptides and Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e944462

Auteurs

Daniele Sola (D)

Department on Translational Medicine, Universityt of Eastern Piedmont, Novara, Italy.

Mattia Bellan (M)

Department on Translational Medicine, Universityt of Eastern Piedmont, Novara, Italy.

Stefania Mai (S)

Laboratory of Metabolic Research, IRCCS Istituto Auxologico Italiano, Oggebbio, Italy.

Rosalba Minisini (R)

Department on Translational Medicine, University of Eastern Piedmont, Novara, Italy.

Mattia Perazzi (M)

Department of Internal Medicine, University of Eastern Piedmont, Novara, Italy.

Amelia Brunani (A)

Laboratory of Metabolic Research, IRCCS Istituto Auxologico Italiano, Oggebbio, Italy.

Sergio Gentilli (S)

Department of Health Sciences, Universityt of Eastern Piedmont, Novara, Italy.

Pier Paolo Sainaghi (PP)

Department on Translational Medicine, Universityt of Eastern Piedmont, Novara, Italy.

Massimo Scacchi (M)

Department of Clinical Sciences and Community Health, University of Milan, Milano, Italy.

Paolo Marzullo (P)

Department on Translational Medicine, Universityt of Eastern Piedmont, Novara, Italy.

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Classifications MeSH