Mast cells in the rat liver are phenotypically heterogeneous and exhibit features of immaturity
Gastrointestinal hypersensitivity to food allergens is a significant but relatively poorly understood allergic disease. Recent evidence from a rat model of IgE‐mediated gastrointestinal hypersensitivity has suggested that hepatic mast cells (HMC) may play an important role in such reactions. The pre...
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description | Gastrointestinal hypersensitivity to food allergens is a significant but relatively poorly understood allergic disease. Recent evidence from a rat model of IgE‐mediated gastrointestinal hypersensitivity has suggested that hepatic mast cells (HMC) may play an important role in such reactions. The present study was undertaken to better define their phenotype. Livers from Australian albino Wistar (AaW), Brown Norway (BN) and PVG/c rats were examined using traditional histological techniques and reverse transcription–polymerase chain reaction (RT‐PCR). Hepatic mast cells were overwhelmingly Alcian blue positive, sensitive to formalin fixation and predominantly rat mast cell protease (RMCP) 1+/2– (AaW 57%; BN 53%). Such a phenotype has previously been associated with an immature mast cell phenotype. A significant number of HMC also stained RMCP 1–/2+ (AaW 15%; BN 19%) or were RMCP 1+/2+ (AaW 24%; BN 26%). In contrast to previous reports, RT‐PCR showed that the liver expressed mRNA of other mast cell proteases, including the chymase RMCP 5 as well as two tryptases, RMCP 6 and RMCP 7. These results suggest that HMC are a heterogeneous population of mast cells with some characteristics previously associated with immature cells. |
doi_str_mv | 10.1046/j.1440-1711.2001.00974.x |
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Recent evidence from a rat model of IgE‐mediated gastrointestinal hypersensitivity has suggested that hepatic mast cells (HMC) may play an important role in such reactions. The present study was undertaken to better define their phenotype. Livers from Australian albino Wistar (AaW), Brown Norway (BN) and PVG/c rats were examined using traditional histological techniques and reverse transcription–polymerase chain reaction (RT‐PCR). Hepatic mast cells were overwhelmingly Alcian blue positive, sensitive to formalin fixation and predominantly rat mast cell protease (RMCP) 1+/2– (AaW 57%; BN 53%). Such a phenotype has previously been associated with an immature mast cell phenotype. A significant number of HMC also stained RMCP 1–/2+ (AaW 15%; BN 19%) or were RMCP 1+/2+ (AaW 24%; BN 26%). In contrast to previous reports, RT‐PCR showed that the liver expressed mRNA of other mast cell proteases, including the chymase RMCP 5 as well as two tryptases, RMCP 6 and RMCP 7. These results suggest that HMC are a heterogeneous population of mast cells with some characteristics previously associated with immature cells.</description><identifier>ISSN: 0818-9641</identifier><identifier>EISSN: 1440-1711</identifier><identifier>DOI: 10.1046/j.1440-1711.2001.00974.x</identifier><identifier>PMID: 11168621</identifier><language>eng</language><publisher>United States: Nature Publishing Group</publisher><subject>Animals ; Chymases ; Female ; Glycosaminoglycans - analysis ; Humans ; Immunohistochemistry ; Liver - cytology ; Male ; Mast Cells - chemistry ; Mast Cells - cytology ; Mast Cells - enzymology ; Mast Cells - immunology ; Phenotype ; Rats ; Rats, Inbred Strains ; Rats, Wistar ; Reverse Transcriptase Polymerase Chain Reaction ; Serine Endopeptidases - analysis ; Serine Endopeptidases - genetics</subject><ispartof>Immunology and cell biology, 2001-02, Vol.79 (1), p.35-40</ispartof><rights>2001 Australasian Society for Immunology Inc.</rights><rights>Copyright Nature Publishing Group Feb 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5156-5ccbff22c411fcdb68ed57be8d3e9568a0f67a21869f3add67ccd6cdc7f2100e3</citedby><cites>FETCH-LOGICAL-c5156-5ccbff22c411fcdb68ed57be8d3e9568a0f67a21869f3add67ccd6cdc7f2100e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1440-1711.2001.00974.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1440-1711.2001.00974.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11168621$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chan, Antonio</creatorcontrib><creatorcontrib>Cooley, Margaret A</creatorcontrib><creatorcontrib>Collins, Andrew M</creatorcontrib><title>Mast cells in the rat liver are phenotypically heterogeneous and exhibit features of immaturity</title><title>Immunology and cell biology</title><addtitle>Immunol Cell Biol</addtitle><description>Gastrointestinal hypersensitivity to food allergens is a significant but relatively poorly understood allergic disease. Recent evidence from a rat model of IgE‐mediated gastrointestinal hypersensitivity has suggested that hepatic mast cells (HMC) may play an important role in such reactions. The present study was undertaken to better define their phenotype. Livers from Australian albino Wistar (AaW), Brown Norway (BN) and PVG/c rats were examined using traditional histological techniques and reverse transcription–polymerase chain reaction (RT‐PCR). Hepatic mast cells were overwhelmingly Alcian blue positive, sensitive to formalin fixation and predominantly rat mast cell protease (RMCP) 1+/2– (AaW 57%; BN 53%). Such a phenotype has previously been associated with an immature mast cell phenotype. A significant number of HMC also stained RMCP 1–/2+ (AaW 15%; BN 19%) or were RMCP 1+/2+ (AaW 24%; BN 26%). In contrast to previous reports, RT‐PCR showed that the liver expressed mRNA of other mast cell proteases, including the chymase RMCP 5 as well as two tryptases, RMCP 6 and RMCP 7. These results suggest that HMC are a heterogeneous population of mast cells with some characteristics previously associated with immature cells.</description><subject>Animals</subject><subject>Chymases</subject><subject>Female</subject><subject>Glycosaminoglycans - analysis</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Liver - cytology</subject><subject>Male</subject><subject>Mast Cells - chemistry</subject><subject>Mast Cells - cytology</subject><subject>Mast Cells - enzymology</subject><subject>Mast Cells - immunology</subject><subject>Phenotype</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Rats, Wistar</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Serine Endopeptidases - analysis</subject><subject>Serine Endopeptidases - genetics</subject><issn>0818-9641</issn><issn>1440-1711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkU2LFDEQhoMo7rj6FyQgeOs21R9J-iQ6-LGwixc9h3RScTL0x5ik1-l_b_fMsAte9BSSPPVWFQ8hFFgOrOLv9jlUFctAAOQFY5Az1ogqPz4hm4ePp2TDJMis4RVckRcx7hljopDlc3IFAFzyAjZE3emYqMGui9QPNO2QBp1o5-8xUB2QHnY4jGk-eKO7bqY7TBjGnzjgOEWqB0vxuPOtT9ShTlPASEdHfd-vF5_ml-SZ013EV5fzmvz4_On79mt2--3LzfbDbWZqqHlWG9M6VxSmAnDGtlyirUWL0pbY1Fxq5rjQBUjeuFJby4UxlhtrhCuAMSyvydtz7iGMvyaMSfU-rmvp06RKMF6KWvB_giCLSjalXMA3f4H7cQrDsoQCIblkJedsoeSZMmGMMaBTh-B7HWYFTK2u1F6tStSqRK2u1MmVOi6lry8NprZH-1h4kbMA78_Ab9_h_N_B6uZu-3F94I8thpObhwhv2jPwB85Nrno</recordid><startdate>200102</startdate><enddate>200102</enddate><creator>Chan, Antonio</creator><creator>Cooley, Margaret A</creator><creator>Collins, Andrew M</creator><general>Nature Publishing Group</general><general>Blackwell Science Ltd</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200102</creationdate><title>Mast cells in the rat liver are phenotypically heterogeneous and exhibit features of immaturity</title><author>Chan, Antonio ; Cooley, Margaret A ; Collins, Andrew M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5156-5ccbff22c411fcdb68ed57be8d3e9568a0f67a21869f3add67ccd6cdc7f2100e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Chymases</topic><topic>Female</topic><topic>Glycosaminoglycans - analysis</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Liver - cytology</topic><topic>Male</topic><topic>Mast Cells - chemistry</topic><topic>Mast Cells - cytology</topic><topic>Mast Cells - enzymology</topic><topic>Mast Cells - immunology</topic><topic>Phenotype</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Rats, Wistar</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Serine Endopeptidases - analysis</topic><topic>Serine Endopeptidases - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan, Antonio</creatorcontrib><creatorcontrib>Cooley, Margaret A</creatorcontrib><creatorcontrib>Collins, Andrew M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Immunology and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan, Antonio</au><au>Cooley, Margaret A</au><au>Collins, Andrew M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mast cells in the rat liver are phenotypically heterogeneous and exhibit features of immaturity</atitle><jtitle>Immunology and cell biology</jtitle><addtitle>Immunol Cell Biol</addtitle><date>2001-02</date><risdate>2001</risdate><volume>79</volume><issue>1</issue><spage>35</spage><epage>40</epage><pages>35-40</pages><issn>0818-9641</issn><eissn>1440-1711</eissn><abstract>Gastrointestinal hypersensitivity to food allergens is a significant but relatively poorly understood allergic disease. Recent evidence from a rat model of IgE‐mediated gastrointestinal hypersensitivity has suggested that hepatic mast cells (HMC) may play an important role in such reactions. The present study was undertaken to better define their phenotype. Livers from Australian albino Wistar (AaW), Brown Norway (BN) and PVG/c rats were examined using traditional histological techniques and reverse transcription–polymerase chain reaction (RT‐PCR). Hepatic mast cells were overwhelmingly Alcian blue positive, sensitive to formalin fixation and predominantly rat mast cell protease (RMCP) 1+/2– (AaW 57%; BN 53%). Such a phenotype has previously been associated with an immature mast cell phenotype. A significant number of HMC also stained RMCP 1–/2+ (AaW 15%; BN 19%) or were RMCP 1+/2+ (AaW 24%; BN 26%). In contrast to previous reports, RT‐PCR showed that the liver expressed mRNA of other mast cell proteases, including the chymase RMCP 5 as well as two tryptases, RMCP 6 and RMCP 7. 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subjects | Animals Chymases Female Glycosaminoglycans - analysis Humans Immunohistochemistry Liver - cytology Male Mast Cells - chemistry Mast Cells - cytology Mast Cells - enzymology Mast Cells - immunology Phenotype Rats Rats, Inbred Strains Rats, Wistar Reverse Transcriptase Polymerase Chain Reaction Serine Endopeptidases - analysis Serine Endopeptidases - genetics |
title | Mast cells in the rat liver are phenotypically heterogeneous and exhibit features of immaturity |
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