Increased Siglec-1 expression in monocytes of patients with primary biliary cirrhosis

Immunol Invest. 2010;39(6):645-60. doi: 10.3109/08820139.2010.485625.

Abstract

Objectives: To evaluate Siglec-1 protein (CD169) and mRNA levels in peripheral blood monocytes of patients with primary biliary cirrhosis (PBC) and investigate its role in PBC pathogenesis by looking for correlations between Siglec-1 expression and key PBC associated biochemical indices.

Methods: FACS analysis was used to identify the percentage of peripheral blood monocytes positive for both CD14 and Siglec-1 in (a) 45 PBC patients, (b) 40 patients with liver cirrhosis after hepatitis B infection and (c) 36 healthy controls. Siglec-1 mRNA was measured by real-time RT-PCR and serum biomarkers by routine biochemistry.

Results: The percentage of CD14-Siglec-1 double positive cells was significantly higher (p< 0.01) in PBC patients than in healthy controls or cirrhosis post-hepatitis patients (13.68 +/- 2.44%, 1.0 +/- 0.2 %, and 4.1 +/- 0.5 %, respectively). Siglec-1 mRNA expression in the PBC group was 3.42 times higher than in healthy controls (p < 0.01).

Conclusion: We investigated the role of Siglec-1 in PBC by assessing its expression in mononuclear cells of PBC patients and levels of secreted cytokines in cell supernatants after Siglec-1 RNA interference. It is possible that elevated Siglec-1 expression in peripheral blood monocytes of PBC patients is correlated with monocyte-mediated inflammatory responses during the development of PBC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Cells, Cultured
  • Cytokines / biosynthesis*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Disease Progression
  • Female
  • Hepatitis B / genetics
  • Hepatitis B / immunology
  • Hepatitis B / metabolism*
  • Hepatitis B / physiopathology
  • Humans
  • Lipopolysaccharide Receptors / biosynthesis
  • Liver Cirrhosis, Biliary / genetics
  • Liver Cirrhosis, Biliary / immunology
  • Liver Cirrhosis, Biliary / metabolism*
  • Liver Cirrhosis, Biliary / physiopathology
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Middle Aged
  • Monocytes / immunology
  • Monocytes / metabolism*
  • Monocytes / pathology
  • RNA, Small Interfering / genetics
  • Receptors, Immunologic / genetics
  • Receptors, Immunologic / metabolism*
  • Sialic Acid Binding Ig-like Lectin 1
  • Up-Regulation

Substances

  • Cytokines
  • Lipopolysaccharide Receptors
  • Membrane Glycoproteins
  • RNA, Small Interfering
  • Receptors, Immunologic
  • SIGLEC1 protein, human
  • Sialic Acid Binding Ig-like Lectin 1