Cellular turnover and expression of hypoxic-inducible factor in acute acalculous and calculous cholecystitis

Crit Care. 2007;11(5):R116. doi: 10.1186/cc6170.

Abstract

Introduction: Epithelial corrective and destructive mechanisms have not been studied in inflammatory gallbladder disease.

Methods: Epithelial apoptosis, cell proliferation and expression of hypoxia-inducible factor (HIF)-1alpha were compared in gallbladders from patients with acute acalculous cholecystitis (AAC; n = 30) and acute calculous cholecystitis (ACC; n = 21), and from patients undergoing surgery for other reasons (normal gallbladders; n = 9), which were removed during open cholecystectomy. The immunohistochemical stains included antibodies to Ki-67 (proliferation), M30 (apoptosis) and HIF-1alpha. Proliferation and apoptosis were expressed as percentages of positive cells. HIF-1alpha expression was expressed as absent, weak, or strong.

Results: Apoptosis (median [25th to 75th percentile]) was significantly increased in AAC (1.31% [0.75% to 1.8%], P < 0.001) and ACC (1.10% [0.63% to 1.64%], P = 0.001), compared with control samples (0.20% [0.07% to 0.45%]. The proliferation rate was significantly increased in AAC (8.0% [4.0% to 17.0%], P < 0.001) and ACC (14% [7.5% to 26.5%], P = 0.001) compared with control samples (1.0% [1.0% to 3.0%]). Strong HIF-1alpha staining was observed in 57% of AAC, in 100% of ACC and in 44% of control specimens (P < 0.001). Intense HIF-1alpha expression was associated with increased cell proliferation (P = 0.002).

Conclusion: Cell proliferation and apoptosis were increased in AAC and ACC, as compared with normal gallbladders. Expression of HIF-1alpha was lower in AAC than in ACC.

Publication types

  • Comparative Study

MeSH terms

  • Acalculous Cholecystitis / metabolism
  • Acalculous Cholecystitis / pathology
  • Apoptosis
  • Biomarkers / metabolism
  • Cell Proliferation
  • Cholecystitis / metabolism*
  • Cholecystitis / pathology
  • Epithelial Cells / metabolism*
  • Female
  • Gallbladder / metabolism*
  • Gallbladder / pathology
  • Humans
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism*
  • Male
  • Middle Aged

Substances

  • Biomarkers
  • Hypoxia-Inducible Factor 1, alpha Subunit