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Immunohistochemical detection of strain-specific major histocompatibility complex class I antigens in paraffin-embedded rat osteochondral tissue
An immunohistochemical method using formalin-fixed, paraffin wax-embedded sections is described for detecting strain-specific major histocompatibility complex class I antigens in knee-joint tissue from DA and Lewis strains of rat. The fixed osteochondral tissues were additionally decalcified in form...
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Published in: | The Histochemical journal 1993-02, Vol.25 (2), p.140-143 |
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container_title | The Histochemical journal |
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creator | GURUSINGHE, C. J HICKEY, M. J HURLEY, J. V O'BRIEN, B. M |
description | An immunohistochemical method using formalin-fixed, paraffin wax-embedded sections is described for detecting strain-specific major histocompatibility complex class I antigens in knee-joint tissue from DA and Lewis strains of rat. The fixed osteochondral tissues were additionally decalcified in formic acid before processing for paraffin wax embedding. For immunohistochemistry, two monoclonal antibodies, one specific for DA class I allele RT1Aa and the other for Lewis class I allele RT1A1, were used together with the avidin-biotin immunoperoxidase procedure. It was necessary to use strain-specific normal rat serum as a diluent for the antibodies to suppress cross-strain recognition. DA-specific antibody stained positively only on DA rat sections, not on Lewis rat sections, and Lewis-specific antibody stained positively only on Lewis rat sections, and not on DA. Positive staining was localized in the bone marrow, osteochondral cells and endothelium. We propose that the use of a decalcification medium may have enhanced the immunoreactivity of the tissue. The method described can be used on sections of allografts from the two strains of rat to assess morphologically the extent of cellular replacement of the graft by the host's cells. |
doi_str_mv | 10.1007/BF00157986 |
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J ; HICKEY, M. J ; HURLEY, J. V ; O'BRIEN, B. M</creator><creatorcontrib>GURUSINGHE, C. J ; HICKEY, M. J ; HURLEY, J. V ; O'BRIEN, B. M</creatorcontrib><description>An immunohistochemical method using formalin-fixed, paraffin wax-embedded sections is described for detecting strain-specific major histocompatibility complex class I antigens in knee-joint tissue from DA and Lewis strains of rat. The fixed osteochondral tissues were additionally decalcified in formic acid before processing for paraffin wax embedding. For immunohistochemistry, two monoclonal antibodies, one specific for DA class I allele RT1Aa and the other for Lewis class I allele RT1A1, were used together with the avidin-biotin immunoperoxidase procedure. It was necessary to use strain-specific normal rat serum as a diluent for the antibodies to suppress cross-strain recognition. DA-specific antibody stained positively only on DA rat sections, not on Lewis rat sections, and Lewis-specific antibody stained positively only on Lewis rat sections, and not on DA. Positive staining was localized in the bone marrow, osteochondral cells and endothelium. We propose that the use of a decalcification medium may have enhanced the immunoreactivity of the tissue. The method described can be used on sections of allografts from the two strains of rat to assess morphologically the extent of cellular replacement of the graft by the host's cells.</description><identifier>ISSN: 0018-2214</identifier><identifier>EISSN: 1573-6865</identifier><identifier>DOI: 10.1007/BF00157986</identifier><identifier>PMID: 8468186</identifier><identifier>CODEN: HISJAE</identifier><language>eng</language><publisher>London: Kluwer</publisher><subject>Animals ; Antibodies, Monoclonal ; Antigens ; Avidin ; Biological and medical sciences ; Biotin ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Histocompatibility antigens (hla, h-2 and other systems) ; Histocompatibility Antigens Class I - analysis ; Immunoenzyme Techniques ; Immunohistochemistry ; Knee Joint - immunology ; Molecular immunology ; Paraffin Embedding ; Rats ; Rats, Inbred Strains ; Species Specificity</subject><ispartof>The Histochemical journal, 1993-02, Vol.25 (2), p.140-143</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c239t-3ec9952f4664b65100e9b9ad3753515a0e6af9e43c32ed5eb12cbc0a4aebb8843</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4665132$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8468186$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GURUSINGHE, C. J</creatorcontrib><creatorcontrib>HICKEY, M. J</creatorcontrib><creatorcontrib>HURLEY, J. V</creatorcontrib><creatorcontrib>O'BRIEN, B. M</creatorcontrib><title>Immunohistochemical detection of strain-specific major histocompatibility complex class I antigens in paraffin-embedded rat osteochondral tissue</title><title>The Histochemical journal</title><addtitle>Histochem J</addtitle><description>An immunohistochemical method using formalin-fixed, paraffin wax-embedded sections is described for detecting strain-specific major histocompatibility complex class I antigens in knee-joint tissue from DA and Lewis strains of rat. The fixed osteochondral tissues were additionally decalcified in formic acid before processing for paraffin wax embedding. For immunohistochemistry, two monoclonal antibodies, one specific for DA class I allele RT1Aa and the other for Lewis class I allele RT1A1, were used together with the avidin-biotin immunoperoxidase procedure. It was necessary to use strain-specific normal rat serum as a diluent for the antibodies to suppress cross-strain recognition. DA-specific antibody stained positively only on DA rat sections, not on Lewis rat sections, and Lewis-specific antibody stained positively only on Lewis rat sections, and not on DA. Positive staining was localized in the bone marrow, osteochondral cells and endothelium. We propose that the use of a decalcification medium may have enhanced the immunoreactivity of the tissue. The method described can be used on sections of allografts from the two strains of rat to assess morphologically the extent of cellular replacement of the graft by the host's cells.</description><subject>Animals</subject><subject>Antibodies, Monoclonal</subject><subject>Antigens</subject><subject>Avidin</subject><subject>Biological and medical sciences</subject><subject>Biotin</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Histocompatibility antigens (hla, h-2 and other systems)</subject><subject>Histocompatibility Antigens Class I - analysis</subject><subject>Immunoenzyme Techniques</subject><subject>Immunohistochemistry</subject><subject>Knee Joint - immunology</subject><subject>Molecular immunology</subject><subject>Paraffin Embedding</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Species Specificity</subject><issn>0018-2214</issn><issn>1573-6865</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LxDAQhoMoun5cvAs5eBKqSdOk7VHFjwXBi56XSTpxs7RNSbLg_gt_spFd1tN8vfPO8BByydktZ6y-e3hmjMu6bdQBmeVEFKpR8pDMcrspypJXJ-Q0xhVjrK1rdUyOm0o1vFEz8jMfhvXoly4mb5Y4OAM97TChSc6P1FsaUwA3FnFC46wzdICVD3S74IcJktOud2lD_6oev6npIUY6pzAm94VjpG6kEwSwNtvgoLHrsKMBEvUxYb7qxy7kq8nFuMZzcmShj3ixi2fk8_np4_G1eHt_mT_evxWmFG0qBJq2laWtlKq0khkDtrqFTtRSSC6BoQLbYiWMKLGTqHlptGFQAWrdNJU4IzdbXxN8jAHtYgpugLBZcLb4o7r4p5rFV1vxtNYDdnvpDmOeX-_mEDNAG2A0Lu5l-UnJRSl-AdVvgy8</recordid><startdate>19930201</startdate><enddate>19930201</enddate><creator>GURUSINGHE, C. J</creator><creator>HICKEY, M. J</creator><creator>HURLEY, J. V</creator><creator>O'BRIEN, B. M</creator><general>Kluwer</general><scope>IQODW</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></search><sort><creationdate>19930201</creationdate><title>Immunohistochemical detection of strain-specific major histocompatibility complex class I antigens in paraffin-embedded rat osteochondral tissue</title><author>GURUSINGHE, C. J ; HICKEY, M. J ; HURLEY, J. V ; O'BRIEN, B. 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Psychology</topic><topic>Fundamental immunology</topic><topic>Histocompatibility antigens (hla, h-2 and other systems)</topic><topic>Histocompatibility Antigens Class I - analysis</topic><topic>Immunoenzyme Techniques</topic><topic>Immunohistochemistry</topic><topic>Knee Joint - immunology</topic><topic>Molecular immunology</topic><topic>Paraffin Embedding</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GURUSINGHE, C. J</creatorcontrib><creatorcontrib>HICKEY, M. J</creatorcontrib><creatorcontrib>HURLEY, J. V</creatorcontrib><creatorcontrib>O'BRIEN, B. 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M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical detection of strain-specific major histocompatibility complex class I antigens in paraffin-embedded rat osteochondral tissue</atitle><jtitle>The Histochemical journal</jtitle><addtitle>Histochem J</addtitle><date>1993-02-01</date><risdate>1993</risdate><volume>25</volume><issue>2</issue><spage>140</spage><epage>143</epage><pages>140-143</pages><issn>0018-2214</issn><eissn>1573-6865</eissn><coden>HISJAE</coden><abstract>An immunohistochemical method using formalin-fixed, paraffin wax-embedded sections is described for detecting strain-specific major histocompatibility complex class I antigens in knee-joint tissue from DA and Lewis strains of rat. The fixed osteochondral tissues were additionally decalcified in formic acid before processing for paraffin wax embedding. For immunohistochemistry, two monoclonal antibodies, one specific for DA class I allele RT1Aa and the other for Lewis class I allele RT1A1, were used together with the avidin-biotin immunoperoxidase procedure. It was necessary to use strain-specific normal rat serum as a diluent for the antibodies to suppress cross-strain recognition. DA-specific antibody stained positively only on DA rat sections, not on Lewis rat sections, and Lewis-specific antibody stained positively only on Lewis rat sections, and not on DA. Positive staining was localized in the bone marrow, osteochondral cells and endothelium. We propose that the use of a decalcification medium may have enhanced the immunoreactivity of the tissue. The method described can be used on sections of allografts from the two strains of rat to assess morphologically the extent of cellular replacement of the graft by the host's cells.</abstract><cop>London</cop><pub>Kluwer</pub><pmid>8468186</pmid><doi>10.1007/BF00157986</doi><tpages>4</tpages></addata></record> |
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subjects | Animals Antibodies, Monoclonal Antigens Avidin Biological and medical sciences Biotin Fundamental and applied biological sciences. Psychology Fundamental immunology Histocompatibility antigens (hla, h-2 and other systems) Histocompatibility Antigens Class I - analysis Immunoenzyme Techniques Immunohistochemistry Knee Joint - immunology Molecular immunology Paraffin Embedding Rats Rats, Inbred Strains Species Specificity |
title | Immunohistochemical detection of strain-specific major histocompatibility complex class I antigens in paraffin-embedded rat osteochondral tissue |
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