Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis

AIM:To examine the expression of intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1(LFA-1)expression on canals of Hering (COH)and bile ductules associated with the autoimmune process of bile duct destruction in primary biliary cirrhosis(PBC). METHODS:Ten wedged l...

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Veröffentlicht in:World journal of gastroenterology : WJG 2005-07, Vol.11 (28), p.4382-4389
Hauptverfasser: Yokomori, Hiroaki, Oda, Masaya, Ogi, Mariko, Wakabayashi, Go, Kawachi, Shigeyuki, Yoshimura, Kazunori, Nagai, Toshihiro, Kitajima, Masaki, Nomura, Masahiko, Hibi, Toshifumi
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container_end_page 4389
container_issue 28
container_start_page 4382
container_title World journal of gastroenterology : WJG
container_volume 11
creator Yokomori, Hiroaki
Oda, Masaya
Ogi, Mariko
Wakabayashi, Go
Kawachi, Shigeyuki
Yoshimura, Kazunori
Nagai, Toshihiro
Kitajima, Masaki
Nomura, Masahiko
Hibi, Toshifumi
description AIM:To examine the expression of intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1(LFA-1)expression on canals of Hering (COH)and bile ductules associated with the autoimmune process of bile duct destruction in primary biliary cirrhosis(PBC). METHODS:Ten wedged liver biopsies of PBC(five cases each of stages 2 and 3)were studied. The liver specimens were processed for transmission electron microscopy. Immunohistochemistry was performed using anti-ICAM-1 and anti-LFA-1 mouse mAbs.In situ hybridization was done to examine the messenger RNA expression of ICAM-1 in formalin-fixed.paraffin-embedded sections using peptide nucleic acid probes and the catalyzed signal amplification (CSA)technique.Immunogold-silver staining for electron microscopy was Derrormed using anti-ICAM and anti-LFA-1 mouse mAbs.The immunogold particles on epithelial cells of bileductules and cholangiocytes of CoH cells were counted and analyzed semi-quantitatively.Western blotting was performed to confirm ICAM-1 protein expression. RESULTS:In liver tissues of PBC patients.immunohi-stochemistry showed aberrant ICAM-1 expression on the plasma membrane of epithelial cells lining bile ductules,and also on mature cholangiocytes but not on hepatocytes in CoH.LFA-1-positive lymphocytes were closely associated with epithelial cells in bile ductules.ICAM-1 expression at protein level was confirmed by Western blot.In situ hybridization demonstrated ICAM-1 mRNA expression in bile ductules and LFA-1 mRNA in lymphocytes infiltrating the bileductules.By immunoelectron microscopy,ICAM-1 was demonstrated on the basal suface of epithelial cells in bile ductules and on the luminal surfaces of cholangiocytes in damaged COH.Cells with intermediate morphology resembling progenitor cells in Coil were not labeled with ICAM-1 and LFA-1. CONCLUSION:De novo expression of ICAM-1 both on mature cholangiocytes in COH and epithelial cells in bile ductules in PBC implies that lymphocyte-induced destruction through adhesion by ICAM-1 and binding of LFA-1-expressing activated lymphocytes takes place not only in bile ductules but also in the COH.
doi_str_mv 10.3748/wjg.v11.i28.4382
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METHODS:Ten wedged liver biopsies of PBC(five cases each of stages 2 and 3)were studied. The liver specimens were processed for transmission electron microscopy. Immunohistochemistry was performed using anti-ICAM-1 and anti-LFA-1 mouse mAbs.In situ hybridization was done to examine the messenger RNA expression of ICAM-1 in formalin-fixed.paraffin-embedded sections using peptide nucleic acid probes and the catalyzed signal amplification (CSA)technique.Immunogold-silver staining for electron microscopy was Derrormed using anti-ICAM and anti-LFA-1 mouse mAbs.The immunogold particles on epithelial cells of bileductules and cholangiocytes of CoH cells were counted and analyzed semi-quantitatively.Western blotting was performed to confirm ICAM-1 protein expression. RESULTS:In liver tissues of PBC patients.immunohi-stochemistry showed aberrant ICAM-1 expression on the plasma membrane of epithelial cells lining bile ductules,and also on mature cholangiocytes but not on hepatocytes in CoH.LFA-1-positive lymphocytes were closely associated with epithelial cells in bile ductules.ICAM-1 expression at protein level was confirmed by Western blot.In situ hybridization demonstrated ICAM-1 mRNA expression in bile ductules and LFA-1 mRNA in lymphocytes infiltrating the bileductules.By immunoelectron microscopy,ICAM-1 was demonstrated on the basal suface of epithelial cells in bile ductules and on the luminal surfaces of cholangiocytes in damaged COH.Cells with intermediate morphology resembling progenitor cells in Coil were not labeled with ICAM-1 and LFA-1. CONCLUSION:De novo expression of ICAM-1 both on mature cholangiocytes in COH and epithelial cells in bile ductules in PBC implies that lymphocyte-induced destruction through adhesion by ICAM-1 and binding of LFA-1-expressing activated lymphocytes takes place not only in bile ductules but also in the COH.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v11.i28.4382</identifier><identifier>PMID: 16038038</identifier><language>eng</language><publisher>United States: Department of Internal Medicine, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Organized Center of Clinical Medicine, International University of Health and Welfare, Tokyo 107-0052, Japan%Laboratory of Pathology, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Department of Surgery, School of Medicine, Keio University, Tokyo 160-00i6, Japan%Physiology, Saitama Medical School, Saitama 350-0495, Japan%Electron Microscopy Laboratory, School of Medicine, Keio University, Tokyo 160-0016, Japan%Department of Internal Medicine, School of Medicine, Keio University, Tokyo 160-0016, Japan</publisher><subject>Aged ; Bile Ducts - pathology ; Bile Ducts - physiology ; Biopsy ; Cell Adhesion - immunology ; Clinical Research ; Female ; Gene Expression ; Humans ; Intercellular Adhesion Molecule-1 - genetics ; Liver Cirrhosis, Biliary - immunology ; Liver Cirrhosis, Biliary - pathology ; Liver Cirrhosis, Biliary - physiopathology ; Lymphocyte Function-Associated Antigen-1 - genetics ; Lymphocytes - immunology ; Lymphocytes - pathology ; Middle Aged ; 基因表达 ; 成熟细胞 ; 组织切片检查 ; 胆管硬化 ; 胆管细胞</subject><ispartof>World journal of gastroenterology : WJG, 2005-07, Vol.11 (28), p.4382-4389</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><rights>The Author(s) 2005. Published by Baishideng Publishing Group Inc. All rights reserved. 2005</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-906479eb250d46d0198df136b03576e41119eef2cd7c82d0e936be98b8a5ed753</citedby><cites>FETCH-LOGICAL-c516t-906479eb250d46d0198df136b03576e41119eef2cd7c82d0e936be98b8a5ed753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434666/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4434666/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27928,27929,53795,53797</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16038038$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yokomori, Hiroaki</creatorcontrib><creatorcontrib>Oda, Masaya</creatorcontrib><creatorcontrib>Ogi, Mariko</creatorcontrib><creatorcontrib>Wakabayashi, Go</creatorcontrib><creatorcontrib>Kawachi, Shigeyuki</creatorcontrib><creatorcontrib>Yoshimura, Kazunori</creatorcontrib><creatorcontrib>Nagai, Toshihiro</creatorcontrib><creatorcontrib>Kitajima, Masaki</creatorcontrib><creatorcontrib>Nomura, Masahiko</creatorcontrib><creatorcontrib>Hibi, Toshifumi</creatorcontrib><title>Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM:To examine the expression of intercellular adhesion molecule-1 (ICAM-1) and lymphocyte function-associated antigen-1(LFA-1)expression on canals of Hering (COH)and bile ductules associated with the autoimmune process of bile duct destruction in primary biliary cirrhosis(PBC). METHODS:Ten wedged liver biopsies of PBC(five cases each of stages 2 and 3)were studied. The liver specimens were processed for transmission electron microscopy. Immunohistochemistry was performed using anti-ICAM-1 and anti-LFA-1 mouse mAbs.In situ hybridization was done to examine the messenger RNA expression of ICAM-1 in formalin-fixed.paraffin-embedded sections using peptide nucleic acid probes and the catalyzed signal amplification (CSA)technique.Immunogold-silver staining for electron microscopy was Derrormed using anti-ICAM and anti-LFA-1 mouse mAbs.The immunogold particles on epithelial cells of bileductules and cholangiocytes of CoH cells were counted and analyzed semi-quantitatively.Western blotting was performed to confirm ICAM-1 protein expression. RESULTS:In liver tissues of PBC patients.immunohi-stochemistry showed aberrant ICAM-1 expression on the plasma membrane of epithelial cells lining bile ductules,and also on mature cholangiocytes but not on hepatocytes in CoH.LFA-1-positive lymphocytes were closely associated with epithelial cells in bile ductules.ICAM-1 expression at protein level was confirmed by Western blot.In situ hybridization demonstrated ICAM-1 mRNA expression in bile ductules and LFA-1 mRNA in lymphocytes infiltrating the bileductules.By immunoelectron microscopy,ICAM-1 was demonstrated on the basal suface of epithelial cells in bile ductules and on the luminal surfaces of cholangiocytes in damaged COH.Cells with intermediate morphology resembling progenitor cells in Coil were not labeled with ICAM-1 and LFA-1. CONCLUSION:De novo expression of ICAM-1 both on mature cholangiocytes in COH and epithelial cells in bile ductules in PBC implies that lymphocyte-induced destruction through adhesion by ICAM-1 and binding of LFA-1-expressing activated lymphocytes takes place not only in bile ductules but also in the COH.</description><subject>Aged</subject><subject>Bile Ducts - pathology</subject><subject>Bile Ducts - physiology</subject><subject>Biopsy</subject><subject>Cell Adhesion - immunology</subject><subject>Clinical Research</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Humans</subject><subject>Intercellular Adhesion Molecule-1 - genetics</subject><subject>Liver Cirrhosis, Biliary - immunology</subject><subject>Liver Cirrhosis, Biliary - pathology</subject><subject>Liver Cirrhosis, Biliary - physiopathology</subject><subject>Lymphocyte Function-Associated Antigen-1 - genetics</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - pathology</subject><subject>Middle Aged</subject><subject>基因表达</subject><subject>成熟细胞</subject><subject>组织切片检查</subject><subject>胆管硬化</subject><subject>胆管细胞</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtv1DAUhSMEokNhzwpZCLHL4FccZ4NUVaWtVIkNrC3Hvkk8JPHUTjrM7-AP48xEPCRLtnPPObm-X5a9JXjLSi4_HXbt9omQraNyy5mkz7INpaTKqeT4ebYhGJd5xWh5kb2KcYcxZaygL7MLIjCTaW2yXzc_9wFidH5EvkHadnA6D74HM_cQ0XLR0xwAmc73emydN8cpFdyIjB51v_juILixRXq0qHY9IDub6eROogPYFtJnv49HFPWwP6U2aB_coMNxMbhlNy6EzkcXX2cvGt1HeLPul9n3Lzffru_yh6-399dXD7kpiJjyCgteVlDTAlsuLCaVtA1hosasKAVwQkgF0FBjSyOpxVClGlSylroAWxbsMvt8zt3P9QDWwDgF3au1L-W1U_9XRtep1j8pzhkXQqSAD-eAgx6bNBm183NIE4kqgaEYF1Rissg-rv8J_nGGOKnBRQN9Gib4OSohsSg4wUmIz0ITfIwBmj-9EKwW4EuuSsBVAq4W4Mny7t83_DWshJPg_ZrZ-bF9TJRUrc2PJlFSJLVHWXrNb_fotyI</recordid><startdate>20050728</startdate><enddate>20050728</enddate><creator>Yokomori, Hiroaki</creator><creator>Oda, Masaya</creator><creator>Ogi, Mariko</creator><creator>Wakabayashi, Go</creator><creator>Kawachi, Shigeyuki</creator><creator>Yoshimura, Kazunori</creator><creator>Nagai, Toshihiro</creator><creator>Kitajima, Masaki</creator><creator>Nomura, Masahiko</creator><creator>Hibi, Toshifumi</creator><general>Department of Internal Medicine, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Organized Center of Clinical Medicine, International University of Health and Welfare, Tokyo 107-0052, Japan%Laboratory of Pathology, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Department of Surgery, School of Medicine, Keio University, Tokyo 160-00i6, Japan%Physiology, Saitama Medical School, Saitama 350-0495, Japan%Electron Microscopy Laboratory, School of Medicine, Keio University, Tokyo 160-0016, Japan%Department of Internal Medicine, School of Medicine, Keio University, Tokyo 160-0016, Japan</general><general>Baishideng Publishing Group Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope><scope>5PM</scope></search><sort><creationdate>20050728</creationdate><title>Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis</title><author>Yokomori, Hiroaki ; 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METHODS:Ten wedged liver biopsies of PBC(five cases each of stages 2 and 3)were studied. The liver specimens were processed for transmission electron microscopy. Immunohistochemistry was performed using anti-ICAM-1 and anti-LFA-1 mouse mAbs.In situ hybridization was done to examine the messenger RNA expression of ICAM-1 in formalin-fixed.paraffin-embedded sections using peptide nucleic acid probes and the catalyzed signal amplification (CSA)technique.Immunogold-silver staining for electron microscopy was Derrormed using anti-ICAM and anti-LFA-1 mouse mAbs.The immunogold particles on epithelial cells of bileductules and cholangiocytes of CoH cells were counted and analyzed semi-quantitatively.Western blotting was performed to confirm ICAM-1 protein expression. RESULTS:In liver tissues of PBC patients.immunohi-stochemistry showed aberrant ICAM-1 expression on the plasma membrane of epithelial cells lining bile ductules,and also on mature cholangiocytes but not on hepatocytes in CoH.LFA-1-positive lymphocytes were closely associated with epithelial cells in bile ductules.ICAM-1 expression at protein level was confirmed by Western blot.In situ hybridization demonstrated ICAM-1 mRNA expression in bile ductules and LFA-1 mRNA in lymphocytes infiltrating the bileductules.By immunoelectron microscopy,ICAM-1 was demonstrated on the basal suface of epithelial cells in bile ductules and on the luminal surfaces of cholangiocytes in damaged COH.Cells with intermediate morphology resembling progenitor cells in Coil were not labeled with ICAM-1 and LFA-1. CONCLUSION:De novo expression of ICAM-1 both on mature cholangiocytes in COH and epithelial cells in bile ductules in PBC implies that lymphocyte-induced destruction through adhesion by ICAM-1 and binding of LFA-1-expressing activated lymphocytes takes place not only in bile ductules but also in the COH.</abstract><cop>United States</cop><pub>Department of Internal Medicine, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Organized Center of Clinical Medicine, International University of Health and Welfare, Tokyo 107-0052, Japan%Laboratory of Pathology, Kitasato Institute Medical Center Hospital, Saitama 364-8501, Japan%Department of Surgery, School of Medicine, Keio University, Tokyo 160-00i6, Japan%Physiology, Saitama Medical School, Saitama 350-0495, Japan%Electron Microscopy Laboratory, School of Medicine, Keio University, Tokyo 160-0016, Japan%Department of Internal Medicine, School of Medicine, Keio University, Tokyo 160-0016, Japan</pub><pmid>16038038</pmid><doi>10.3748/wjg.v11.i28.4382</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Bile Ducts - pathology
Bile Ducts - physiology
Biopsy
Cell Adhesion - immunology
Clinical Research
Female
Gene Expression
Humans
Intercellular Adhesion Molecule-1 - genetics
Liver Cirrhosis, Biliary - immunology
Liver Cirrhosis, Biliary - pathology
Liver Cirrhosis, Biliary - physiopathology
Lymphocyte Function-Associated Antigen-1 - genetics
Lymphocytes - immunology
Lymphocytes - pathology
Middle Aged
基因表达
成熟细胞
组织切片检查
胆管硬化
胆管细胞
title Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis
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