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...
Gespeichert in:
Veröffentlicht in: | World journal of gastroenterology : WJG 2005-07, Vol.11 (28), p.4382-4389 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>wanfang_jour_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4434666</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>18012344</cqvip_id><wanfj_id>wjg200528016</wanfj_id><sourcerecordid>wjg200528016</sourcerecordid><originalsourceid>FETCH-LOGICAL-c516t-906479eb250d46d0198df136b03576e41119eef2cd7c82d0e936be98b8a5ed753</originalsourceid><addsrcrecordid>eNpVkUtv1DAUhSMEokNhzwpZCLHL4FccZ4NUVaWtVIkNrC3Hvkk8JPHUTjrM7-AP48xEPCRLtnPPObm-X5a9JXjLSi4_HXbt9omQraNyy5mkz7INpaTKqeT4ebYhGJd5xWh5kb2KcYcxZaygL7MLIjCTaW2yXzc_9wFidH5EvkHadnA6D74HM_cQ0XLR0xwAmc73emydN8cpFdyIjB51v_juILixRXq0qHY9IDub6eROogPYFtJnv49HFPWwP6U2aB_coMNxMbhlNy6EzkcXX2cvGt1HeLPul9n3Lzffru_yh6-399dXD7kpiJjyCgteVlDTAlsuLCaVtA1hosasKAVwQkgF0FBjSyOpxVClGlSylroAWxbsMvt8zt3P9QDWwDgF3au1L-W1U_9XRtep1j8pzhkXQqSAD-eAgx6bNBm183NIE4kqgaEYF1Rissg-rv8J_nGGOKnBRQN9Gib4OSohsSg4wUmIz0ITfIwBmj-9EKwW4EuuSsBVAq4W4Mny7t83_DWshJPg_ZrZ-bF9TJRUrc2PJlFSJLVHWXrNb_fotyI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68065410</pqid></control><display><type>article</type><title>Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis</title><source>MEDLINE</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Yokomori, Hiroaki ; Oda, Masaya ; Ogi, Mariko ; Wakabayashi, Go ; Kawachi, Shigeyuki ; Yoshimura, Kazunori ; Nagai, Toshihiro ; Kitajima, Masaki ; Nomura, Masahiko ; Hibi, Toshifumi</creator><creatorcontrib>Yokomori, Hiroaki ; Oda, Masaya ; Ogi, Mariko ; Wakabayashi, Go ; Kawachi, Shigeyuki ; Yoshimura, Kazunori ; Nagai, Toshihiro ; Kitajima, Masaki ; Nomura, Masahiko ; Hibi, Toshifumi</creatorcontrib><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><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 ; Oda, Masaya ; Ogi, Mariko ; Wakabayashi, Go ; Kawachi, Shigeyuki ; Yoshimura, Kazunori ; Nagai, Toshihiro ; Kitajima, Masaki ; Nomura, Masahiko ; Hibi, Toshifumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-906479eb250d46d0198df136b03576e41119eef2cd7c82d0e936be98b8a5ed753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aged</topic><topic>Bile Ducts - pathology</topic><topic>Bile Ducts - physiology</topic><topic>Biopsy</topic><topic>Cell Adhesion - immunology</topic><topic>Clinical Research</topic><topic>Female</topic><topic>Gene Expression</topic><topic>Humans</topic><topic>Intercellular Adhesion Molecule-1 - genetics</topic><topic>Liver Cirrhosis, Biliary - immunology</topic><topic>Liver Cirrhosis, Biliary - pathology</topic><topic>Liver Cirrhosis, Biliary - physiopathology</topic><topic>Lymphocyte Function-Associated Antigen-1 - genetics</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - pathology</topic><topic>Middle Aged</topic><topic>基因表达</topic><topic>成熟细胞</topic><topic>组织切片检查</topic><topic>胆管硬化</topic><topic>胆管细胞</topic><toplevel>online_resources</toplevel><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><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yokomori, Hiroaki</au><au>Oda, Masaya</au><au>Ogi, Mariko</au><au>Wakabayashi, Go</au><au>Kawachi, Shigeyuki</au><au>Yoshimura, Kazunori</au><au>Nagai, Toshihiro</au><au>Kitajima, Masaki</au><au>Nomura, Masahiko</au><au>Hibi, Toshifumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of adhesion molecules on mature cholangiocytes in canal of Hering and bile ductules in wedge biopsy samples of primary biliary cirrhosis</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2005-07-28</date><risdate>2005</risdate><volume>11</volume><issue>28</issue><spage>4382</spage><epage>4389</epage><pages>4382-4389</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 1007-9327 |
ispartof | World journal of gastroenterology : WJG, 2005-07, Vol.11 (28), p.4382-4389 |
issn | 1007-9327 2219-2840 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4434666 |
source | MEDLINE; PubMed Central; Alma/SFX Local Collection |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-16T19%3A01%3A20IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wanfang_jour_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Expression%20of%20adhesion%20molecules%20on%20mature%20cholangiocytes%20in%20canal%20of%20Hering%20and%20bile%20ductules%20in%20wedge%20biopsy%20samples%20of%20primary%20biliary%20cirrhosis&rft.jtitle=World%20journal%20of%20gastroenterology%20:%20WJG&rft.au=Yokomori,%20Hiroaki&rft.date=2005-07-28&rft.volume=11&rft.issue=28&rft.spage=4382&rft.epage=4389&rft.pages=4382-4389&rft.issn=1007-9327&rft.eissn=2219-2840&rft_id=info:doi/10.3748/wjg.v11.i28.4382&rft_dat=%3Cwanfang_jour_pubme%3Ewjg200528016%3C/wanfang_jour_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=68065410&rft_id=info:pmid/16038038&rft_cqvip_id=18012344&rft_wanfj_id=wjg200528016&rfr_iscdi=true |