Leptin receptor isoforms mRNA expression in peripheral blood mononuclear cells from patients with chronic viral hepatitis

• Published in: Experimental biology and medicine (Maywood, N.J.) Vol. 231; no. 10; p. 1653
• Main Authors: Stefanou, Nikolaos, Satra, Maria, Papanikolaou, Vassilios, Kalala, Fani, Gatselis, Nikolaos, Germenis, Anastasios, Dalekos, George N, Tsezou, Aspasia
• Format: Journal Article
• Language: English
• Published: England 01-11-2006
• Subjects: Female; Fibrosis - pathology; Flow Cytometry; Gene Expression Regulation; Hepatitis B, Chronic - blood; Hepatitis B, Chronic - genetics; Hepatitis B, Chronic - physiopathology; Hepatitis C, Chronic - blood; Hepatitis C, Chronic - genetics; Hepatitis C, Chronic - physiopathology; Humans; Leukocytes, Mononuclear - metabolism; Liver Diseases - immunology; Liver Diseases - pathology; Liver Diseases - virology; Middle Aged; Protein Isoforms - blood; Protein Isoforms - genetics; Receptors, Cell Surface - blood; Receptors, Cell Surface - genetics; Receptors, Leptin; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - blood; RNA, Messenger - genetics
• ISSN: 1535-3702
• DOI: 10.1177/153537020623101011

There is accumulating evidence that leptin has a pleiotropic role in hematopoiesis, immune response, fibrogenesis, and hepatocarcinogenesis. We investigated the expression of leptin and leptin receptor (OB-R) at the protein level by flow cytometry and also quantified by real-time reverse transcriptase-polymerase chain reaction (RT-PCR) the two major leptin receptor isoforms (OB-Rl, OB-Rs) in peripheral blood mononuclear cells (PBMCs) of patients with hepatitis B (HBV; n = 31), hepatitis C (HCV; n = 34), and nonviral liver disease (n = 25), and healthy controls (n = 36), as well as in liver tissues of HBV (n = 8), HCV (n = 7), and healthy individuals (n = 6). Serum leptin levels were measured in all participants (N = 126). We observed significantly lower OB-Rl and OB-Rs mRNA levels in PBMCs of HBV and HCV patients compared with healthy controls and nonviral liver disease patients (P < 0.05). Flow cytometry analysis confirmed the real-time RT-PCR results. Expression of leptin and OB-Rl was significantly increased in viral hepatitis liver tissues compared with healthy tissues (P < 0.01). OB-Rl mRNA levels were not associated with hepatitis patients' clinical status (inactive, chronic hepatitis, or cirrhosis). We also found decreased serum leptin in HBV and HCV patients compared with healthy individuals and the nonviral liver disease group. Leptin was expressed in 3 of 34 HCV (8.8%) and 19 of 25 (76%) nonviral liver disease patients. Moreover, expression of OB-Rl and OB-Rs were associated when all individuals were grouped together (r = 0.78, P < 0.001). In conclusion, our findings may suggest the involvement of the leptin system in the immunopathology of chronic viral hepatitis.