TGF-β/Smad signaling pathway in fatty liver disease: a case-control study

• DOI: 10.1007/s11033-024-09973-w
• Publication Date: 2024-10-01T13:02:15Z
• Authors: Amir Mohammad Zargar; Zahra Ali; Aida Fallah; Sina Mohagheghi
• Keywords: Male; Adult; Connective Tissue Growth Factor; Smad Proteins; Smad2 Protein; Middle Aged; Transforming Growth Factor beta1; Fatty Liver; Transforming Growth Factor beta3; Gene Expression Regulation; Transforming Growth Factor beta; Non-alcoholic Fatty Liver Disease; Case-Control Studies; Humans; Female; Smad3 Protein; Signal Transduction

Fatty liver disease is a metabolic disorder that recently has been classified into two categories: metabolic dysfunction-associated fatty liver disease (MAFLD) and non-MAFLD. TGF-β signaling pathway is likely a significant factor in the pathogenesis of this condition, exerting its effects through its downstream signaling proteins, Smad2/3. Accordingly, this study aimed to investigate the TGF-β signaling pathway in the white blood cells (WBCs) of patients with MAFLD compared to those with non-MAFLD and control groups.In this study, 41 patients with fatty liver were evaluated, comprising 22 patients with MAFLD and 19 patients with non-MAFLD, and compared to 22 healthy controls. Gene expression of TGF-β1, TGF-β3, and CTGF were quantified using qRT-PCR, and the protein expressions of Smad2/3 and P-Smad2/3 were analyzed using western blotting. Gene expression analysis revealed a significant decrease in the gene expressions of the TGF-β1 and TGF-β3 and an increase in CTGF gene expression in patients with MAFLD and non-MAFLD compared to the control group. Notably, the Smad2/3 protein expression was significantly higher in the non-MAFLD group compared to the control group (P < 0.05). On the other hand, the P-smad2/3 protein expression was significantly elevated in the MAFLD group compared to the control group (P < 0.001).TGF-β signaling pathway in WBCs of patients with fatty liver are affected by a complex signaling pathway. However, metabolic factors most probably affect TGF-β1 gene expression and its downstream signaling proteins more than TGF-β3.