Distribution of type V secretory phospholipase A2 expression in human hepatocytes damaged by liver disease

J Gastroenterol Hepatol. 2004 Oct;19(10):1140-9. doi: 10.1111/j.1440-1746.2004.03435.x.

Abstract

Background and aim: Type V secretory phospholipase A2 (sPLA2-V) is a key enzyme in the arachidonate cascade. However, the distribution of sPLA2-V in human liver has not yet been investigated. In this study, the significance of sPLA2-V expression in human hepatocytes damaged by liver disease was investigated.

Methods: Samples of liver tissue from patients with chronic hepatitis B and C, hepatitis virus-related liver cirrhosis, and congestive hepatocyte injury were immunostained with antibodies against sPLA2-V, cyclooxygenase (COX)-2, hepatitis viral antigens, transforming growth factor (TGF)-beta1, interleukin (IL)-1beta and tumor necrosis factor (TNF)-alpha.

Results: In chronic hepatitis patients, sPLA2-V-positive hepatocytes were scattered in the liver lobules, while cyclooxygenase-2, IL-1beta, and TNF-alpha were diffusely expressed. Hepatocytes around necroinflammatory lesions were strongly positive for sPLA2-V. Some sPLA2-V-positive hepatocytes were also positive for viral antigens. TGF-beta1 was expressed only in fibrotic lesions. The pattern of distribution of these proteins in liver cirrhosis patients was similar to that in chronic hepatitis patients, but sPLA2-V expression tended to be more intense than in chronic hepatitis. In the congestive liver, sPLA2-V, COX-2, and the two cytokines were diffusely expressed in surviving hepatocytes.

Conclusions: sPLA2-V expression in hepatocytes is induced by viral infection, fibrosis, and circulatory disturbance. Immunostaining using sPLA2-V antibody is useful for the detection of injured hepatocytes in patients with liver diseases.

MeSH terms

  • Adult
  • Aged
  • Cyclooxygenase 2
  • Cytokines / biosynthesis
  • Female
  • Group V Phospholipases A2
  • Hepatitis Antigens / biosynthesis
  • Hepatitis, Viral, Human / pathology
  • Hepatitis, Viral, Human / physiopathology
  • Hepatocytes / metabolism*
  • Humans
  • Liver Cirrhosis / pathology
  • Liver Cirrhosis / physiopathology
  • Liver Diseases / pathology
  • Liver Diseases / physiopathology*
  • Male
  • Membrane Proteins
  • Middle Aged
  • Phospholipases A / biosynthesis*
  • Phospholipases A2
  • Prostaglandin-Endoperoxide Synthases / biosynthesis

Substances

  • Cytokines
  • Hepatitis Antigens
  • Membrane Proteins
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Prostaglandin-Endoperoxide Synthases
  • Phospholipases A
  • Group V Phospholipases A2
  • Phospholipases A2
  • phospholipase A2-V, Trimeresurus