Abstract | OBJECTIVE: MATERIALS AND METHODS: RESULTS: In PBC liver samples, immunohistochemistry showed aberrant ICAM-1 expression on bile duct epithelial plasma membrane and also luminal sites of endothelial plasma membrane of terminal portal venules. Western blot confirmed ICAM-1 protein expression. LFA-1-positive lymphocytes were associated with epithelial cells of septal and interlobular bile ducts. Immunoelectron microscopy localized ICAM-1 on the luminal and basal surfaces as well as on lymphocytes around damaged bile duct epithelial cells, and LFA-1 on lymphocytes around damaged bile ducts. Messenger RNA expression of ICAM-1 was demonstrated in bile ducts, and LFA-1 in lymphocytes around bile ducts. CONCLUSION: De novo expression of ICAM-1 and LFA-1 at protein and mRNA levels in PBC may imply an inductive role of ICAM-1 through binding with its ligand LFA-1 in the extravasation of activated lymphocytes and lymphocyte-mediated bile duct destruction.
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Authors | Hiroaki Yokomori, Masaya Oda, Kazunori Yoshimura, Masahiko Nomura, Mariko Ogi, Go Wakabayashi, Masaki Kitajima, Hiromasa Ishii |
Journal | Internal medicine (Tokyo, Japan)
(Intern Med)
Vol. 42
Issue 10
Pg. 947-54
(Oct 2003)
ISSN: 0918-2918 [Print] Japan |
PMID | 14606706
(Publication Type: Journal Article)
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Chemical References |
- Lymphocyte Function-Associated Antigen-1
- RNA, Messenger
- Intercellular Adhesion Molecule-1
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Topics |
- Adult
- Aged
- Autoimmune Diseases
(complications, immunology)
- Female
- Humans
- Intercellular Adhesion Molecule-1
(biosynthesis, immunology)
- Liver Cirrhosis, Biliary
(immunology)
- Lymphocyte Function-Associated Antigen-1
(biosynthesis, immunology)
- Male
- Middle Aged
- RNA, Messenger
(immunology)
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