Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (41): 7677-7680.doi: 10.3969/j.issn.1673-8225.2011.41.019

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Nuclear factor-kappa B and cellular Fas-associated death domain-like interleukin-1 beta-convening enzyme inhibitory protein expression in fibroblasts from normal bile duct and biliary scar tissue of Diannan small-eared pigs

Hu Ping-hai1, Yang Hui2, Li Li3   

  1. 1Kunming Medical College, Kunming  650118, Yunnan Province, China
    2Kunhua Hospital Affiliated to Kunming Medical University, Kunming  650032, Yunnan Province, China
    3Ganmei Hospital Affliated to Kunming Medical Unitersity, Kunming  650034, Yunnan Province, China
  • Received:2011-05-17 Revised:2011-07-19 Online:2011-10-08 Published:2011-10-08
  • About author:Hu Ping-hai☆, Studying for doctorate, Attending physician, Kunming Medical College, Kunming 650032, Yunnan Province, China hph1111@sina.com

Abstract:

BACKGROUND: Biliary scar formation results in destroyed balance between cell proliferation and apoptosis, in particular, fibroblasts greatly proliferate and excessively secrete collagen. 
OBJECTIVE: To compare nuclear factor-kappa B (NF-κB) and cellular Fas-associated death domain-like interleukin-1 beta-convening enzyme (FLICE) inhibitory protein expression in fibroblasts from normal bile duct and biliary scar tissue of Diannan small-eared pigs.
METHODS: Eight Diannan small-eared pigs were randomly divided into model group and normal control group. In the model group, biliary scar tissue-derived fibroblasts were harvested by establishing bile duct injury models. In the normal control group, normal bile duct fibroblasts were harvested.
RESULTS AND CONCLUSION: Compared with normal bile duct-derived fibroblasts, NF-κB and FLICE inhibitory protein expression was greater in the biliary scar tissue-derived fibroblast. These findings suggest that after biliary duct injury, NF-κB expression was increased and FLICE inhibitory protein was overexpressed, which leads to reduction in bile duct fibroblasts and finally results in biliary scar formation.

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