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Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine

It has been reported that levels of soluble intercellular adhesion molecule-1 (ICAM-1) in the blood are elevated in hepatocellular carcinoma patients. In the present study, serial observations of the localization of ICAM-1 in the liver were made by light and electron microscopy in rats with carcinog...

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Autores principales: Matsuoka, Shunichi, Matsumura, Hiroshi, Arakawa, Yasuo, Nakamura, Hitomi, Nirei, Kazushige, Yamagami, Hiroaki, Ogawa, Masahiro, Nakajima, Noriko, Amaki, Shunichi, Tanaka, Naohide, Moriyama, Mitsuhiko
Formato: Texto
Lenguaje:English
Publicado: the Society for Free Radical Research Japan 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735624/
https://www.ncbi.nlm.nih.gov/pubmed/19794920
http://dx.doi.org/10.3164/jcbn.08-247
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author Matsuoka, Shunichi
Matsumura, Hiroshi
Arakawa, Yasuo
Nakamura, Hitomi
Nirei, Kazushige
Yamagami, Hiroaki
Ogawa, Masahiro
Nakajima, Noriko
Amaki, Shunichi
Tanaka, Naohide
Moriyama, Mitsuhiko
author_facet Matsuoka, Shunichi
Matsumura, Hiroshi
Arakawa, Yasuo
Nakamura, Hitomi
Nirei, Kazushige
Yamagami, Hiroaki
Ogawa, Masahiro
Nakajima, Noriko
Amaki, Shunichi
Tanaka, Naohide
Moriyama, Mitsuhiko
author_sort Matsuoka, Shunichi
collection PubMed
description It has been reported that levels of soluble intercellular adhesion molecule-1 (ICAM-1) in the blood are elevated in hepatocellular carcinoma patients. In the present study, serial observations of the localization of ICAM-1 in the liver were made by light and electron microscopy in rats with carcinogen-induced cancer. Male Fisher rats were given diethylnitrosamine (DEN) orally in their drinking water. Rats were sacrificed at 6, 8, 12, or 14 weeks after the start of DEN administration and the liver tissue was collected. ICAM-1 expression in liver was assessed using indirect immunoperoxidase staining with anti-rat ICAM-1 antibody. Although ICAM-1 expression by endothelial cells in livers of DEN-treated rats was lower than in the control group at 8 weeks, it was higher in the membrane and cytoplasm of hepatocytes. The expression of ICAM-1 in mesenchymal cells was decreased, paralleling development of cellular atypia, whereas in hepatocyte membranes and cytoplasm it was increased in these atypia. ICAM-1 was localized to the cytoplasm of cancer cells, but to the membrane of hepatocytes in the treated livers at 14 weeks. Furthermore, the levels of ICAM-1 in mesenchymal cells tended to be lower in the cancerous area than in the atypical hyperplastic nodule, and were reduced as the density of cell atypia increased, in comparison to cells in areas without cancerous nodules. We concluded that ICAM-1 may be influenced the development of cancer induced in the rat liver by a chemical carcinogen.
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spelling pubmed-27356242009-09-30 Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine Matsuoka, Shunichi Matsumura, Hiroshi Arakawa, Yasuo Nakamura, Hitomi Nirei, Kazushige Yamagami, Hiroaki Ogawa, Masahiro Nakajima, Noriko Amaki, Shunichi Tanaka, Naohide Moriyama, Mitsuhiko J Clin Biochem Nutr Original Article It has been reported that levels of soluble intercellular adhesion molecule-1 (ICAM-1) in the blood are elevated in hepatocellular carcinoma patients. In the present study, serial observations of the localization of ICAM-1 in the liver were made by light and electron microscopy in rats with carcinogen-induced cancer. Male Fisher rats were given diethylnitrosamine (DEN) orally in their drinking water. Rats were sacrificed at 6, 8, 12, or 14 weeks after the start of DEN administration and the liver tissue was collected. ICAM-1 expression in liver was assessed using indirect immunoperoxidase staining with anti-rat ICAM-1 antibody. Although ICAM-1 expression by endothelial cells in livers of DEN-treated rats was lower than in the control group at 8 weeks, it was higher in the membrane and cytoplasm of hepatocytes. The expression of ICAM-1 in mesenchymal cells was decreased, paralleling development of cellular atypia, whereas in hepatocyte membranes and cytoplasm it was increased in these atypia. ICAM-1 was localized to the cytoplasm of cancer cells, but to the membrane of hepatocytes in the treated livers at 14 weeks. Furthermore, the levels of ICAM-1 in mesenchymal cells tended to be lower in the cancerous area than in the atypical hyperplastic nodule, and were reduced as the density of cell atypia increased, in comparison to cells in areas without cancerous nodules. We concluded that ICAM-1 may be influenced the development of cancer induced in the rat liver by a chemical carcinogen. the Society for Free Radical Research Japan 2009-09 2009-08-28 /pmc/articles/PMC2735624/ /pubmed/19794920 http://dx.doi.org/10.3164/jcbn.08-247 Text en Copyright © 2009 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Matsuoka, Shunichi
Matsumura, Hiroshi
Arakawa, Yasuo
Nakamura, Hitomi
Nirei, Kazushige
Yamagami, Hiroaki
Ogawa, Masahiro
Nakajima, Noriko
Amaki, Shunichi
Tanaka, Naohide
Moriyama, Mitsuhiko
Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title_full Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title_fullStr Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title_full_unstemmed Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title_short Expression of Intercellular Adhesion Molecule-1 in the Livers of Rats Treated with Diethylnitrosamine
title_sort expression of intercellular adhesion molecule-1 in the livers of rats treated with diethylnitrosamine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735624/
https://www.ncbi.nlm.nih.gov/pubmed/19794920
http://dx.doi.org/10.3164/jcbn.08-247
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