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Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited
Mucosal mast cells (MMC) play an important role in the immune response against selected species of intestinal nematode. The kinetics with which different strains of inbred mice resolve infection with Trichinella spiralis correlates with their ability to mount MMC responses in the intestinal mucosa....
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Published in: | Journal of helminthology 2003-06, Vol.77 (2), p.155-161 |
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description | Mucosal mast cells (MMC) play an important role in the immune response against selected species of intestinal nematode. The kinetics with which different strains of inbred mice resolve infection with Trichinella spiralis correlates with their ability to mount MMC responses in the intestinal mucosa. Homologues of MMC that express and constitutively secrete abundant amounts of the granule chymase, mouse mast cell protease-1 (mMCP-1), can be generated in vitro from bone marrow cultures supplemented with interleukins-3 and -9, stem cell factor and transforming growth factor-β1. Using the enhanced growth characteristics of these MMC homologues, a novel limiting dilution assay for mast cell precursor (MCp) frequency has been developed. The assay is highly specific, in that cultures containing mast cells are identified with mMCP-1 specific antibody, and almost three-fold more sensitive than previously published systems. MCp frequencies were compared in BALB/c and C57/BL10 strains of mice that, respectively, respond rapidly and slowly to infection with T. spiralis. MCp frequency (1/378 bone marrow cells) was significantly greater (P |
doi_str_mv | 10.1079/JOH2002160 |
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The kinetics with which different strains of inbred mice resolve infection with Trichinella spiralis correlates with their ability to mount MMC responses in the intestinal mucosa. Homologues of MMC that express and constitutively secrete abundant amounts of the granule chymase, mouse mast cell protease-1 (mMCP-1), can be generated in vitro from bone marrow cultures supplemented with interleukins-3 and -9, stem cell factor and transforming growth factor-β1. Using the enhanced growth characteristics of these MMC homologues, a novel limiting dilution assay for mast cell precursor (MCp) frequency has been developed. The assay is highly specific, in that cultures containing mast cells are identified with mMCP-1 specific antibody, and almost three-fold more sensitive than previously published systems. MCp frequencies were compared in BALB/c and C57/BL10 strains of mice that, respectively, respond rapidly and slowly to infection with T. spiralis. MCp frequency (1/378 bone marrow cells) was significantly greater (P<0.05) in BALB/c than C57/BL10 mice (frequency: 1/751). Similarly the rate of growth of MMC homologues and the production of mMCP-1 was significantly (P<0.05) greater in BALB/c than in C57/BL10 bone marrow cultures.</description><identifier>ISSN: 0022-149X</identifier><identifier>EISSN: 1475-2697</identifier><identifier>DOI: 10.1079/JOH2002160</identifier><identifier>PMID: 12756069</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Animals ; Antibodies - analysis ; Bone Marrow Cells ; Cell Differentiation ; Cells, Cultured ; Chymases ; Culture Media ; Fluorescent Antibody Technique ; Interleukin-3 ; Interleukin-9 ; Intestinal Diseases, Parasitic - immunology ; Intestinal Mucosa - immunology ; Male ; Mast Cells - immunology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Serine Endopeptidases - immunology ; Species Specificity ; Stem Cell Factor ; Transforming Growth Factor beta ; Trichinella spiralis ; Trichinellosis - immunology</subject><ispartof>Journal of helminthology, 2003-06, Vol.77 (2), p.155-161</ispartof><rights>Cambridge University Press 2003</rights><rights>Cambridge University Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683</citedby><cites>FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0022149X03000258/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,72960</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12756069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brown, J.K.</creatorcontrib><creatorcontrib>Wright, S.H.</creatorcontrib><creatorcontrib>Miller, H.R.P.</creatorcontrib><title>Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited</title><title>Journal of helminthology</title><addtitle>J. Helminthol</addtitle><description>Mucosal mast cells (MMC) play an important role in the immune response against selected species of intestinal nematode. The kinetics with which different strains of inbred mice resolve infection with Trichinella spiralis correlates with their ability to mount MMC responses in the intestinal mucosa. Homologues of MMC that express and constitutively secrete abundant amounts of the granule chymase, mouse mast cell protease-1 (mMCP-1), can be generated in vitro from bone marrow cultures supplemented with interleukins-3 and -9, stem cell factor and transforming growth factor-β1. Using the enhanced growth characteristics of these MMC homologues, a novel limiting dilution assay for mast cell precursor (MCp) frequency has been developed. The assay is highly specific, in that cultures containing mast cells are identified with mMCP-1 specific antibody, and almost three-fold more sensitive than previously published systems. MCp frequencies were compared in BALB/c and C57/BL10 strains of mice that, respectively, respond rapidly and slowly to infection with T. spiralis. MCp frequency (1/378 bone marrow cells) was significantly greater (P<0.05) in BALB/c than C57/BL10 mice (frequency: 1/751). Similarly the rate of growth of MMC homologues and the production of mMCP-1 was significantly (P<0.05) greater in BALB/c than in C57/BL10 bone marrow cultures.</description><subject>Animals</subject><subject>Antibodies - analysis</subject><subject>Bone Marrow Cells</subject><subject>Cell Differentiation</subject><subject>Cells, Cultured</subject><subject>Chymases</subject><subject>Culture Media</subject><subject>Fluorescent Antibody Technique</subject><subject>Interleukin-3</subject><subject>Interleukin-9</subject><subject>Intestinal Diseases, Parasitic - immunology</subject><subject>Intestinal Mucosa - immunology</subject><subject>Male</subject><subject>Mast Cells - immunology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Serine Endopeptidases - immunology</subject><subject>Species Specificity</subject><subject>Stem Cell Factor</subject><subject>Transforming Growth Factor beta</subject><subject>Trichinella spiralis</subject><subject>Trichinellosis - immunology</subject><issn>0022-149X</issn><issn>1475-2697</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpt0V1rFDEUBuAgFru23vgDJHjhhTiak8-md1rsVt1aBAXxJmQyJ5K6M7NNZsT--6bs4oJ4FUge3vOSQ8hTYK-BGfvm49UFZ4yDZg_IAqRRDdfWPCSLeskbkPb7IXlcyjVjTABXj8ghcKM003ZBbi7nMBa_pr0vEw24Xhfqh44O2Ptp7JCmIWKY0jic0jJln4ambDCkmALtUoyYcQhYKtsn0E3GMOcyZhoz3sxV3NKMv1NJE3bH5CD6dcEnu_OIfDt___XsolldLT-cvV01QSqYGhFbr7HVCJbFTlkrIChxEiDqVhqpZRtMDCoIqQUIrWVUXAUFnQLopD4RR-TFNneTx9qhTK5P5b6eH3CcizOCWw3GVPj8H3g9znmo3RwHIa2RSlf0cotCHkvJGN0mp97nWwfM3W_B7bdQ8bNd4tz22O3p7tsraLYglQn__H33-ZfTRhjl9PKLs-erH8t3nz85Uf2r3XTftzl1P3Hf8T_z7wBpTp-m</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Brown, J.K.</creator><creator>Wright, S.H.</creator><creator>Miller, H.R.P.</creator><general>Cambridge University Press</general><scope>BSCLL</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>3V.</scope><scope>7QG</scope><scope>7SN</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H95</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L.G</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200306</creationdate><title>Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited</title><author>Brown, J.K. ; Wright, S.H. ; Miller, H.R.P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antibodies - analysis</topic><topic>Bone Marrow Cells</topic><topic>Cell Differentiation</topic><topic>Cells, Cultured</topic><topic>Chymases</topic><topic>Culture Media</topic><topic>Fluorescent Antibody Technique</topic><topic>Interleukin-3</topic><topic>Interleukin-9</topic><topic>Intestinal Diseases, Parasitic - immunology</topic><topic>Intestinal Mucosa - immunology</topic><topic>Male</topic><topic>Mast Cells - immunology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Serine Endopeptidases - immunology</topic><topic>Species Specificity</topic><topic>Stem Cell Factor</topic><topic>Transforming Growth Factor beta</topic><topic>Trichinella spiralis</topic><topic>Trichinellosis - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brown, J.K.</creatorcontrib><creatorcontrib>Wright, S.H.</creatorcontrib><creatorcontrib>Miller, H.R.P.</creatorcontrib><collection>Istex</collection><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>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Public Health Database</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)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><jtitle>Journal of helminthology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brown, J.K.</au><au>Wright, S.H.</au><au>Miller, H.R.P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited</atitle><jtitle>Journal of helminthology</jtitle><addtitle>J. Helminthol</addtitle><date>2003-06</date><risdate>2003</risdate><volume>77</volume><issue>2</issue><spage>155</spage><epage>161</epage><pages>155-161</pages><issn>0022-149X</issn><eissn>1475-2697</eissn><abstract>Mucosal mast cells (MMC) play an important role in the immune response against selected species of intestinal nematode. The kinetics with which different strains of inbred mice resolve infection with Trichinella spiralis correlates with their ability to mount MMC responses in the intestinal mucosa. Homologues of MMC that express and constitutively secrete abundant amounts of the granule chymase, mouse mast cell protease-1 (mMCP-1), can be generated in vitro from bone marrow cultures supplemented with interleukins-3 and -9, stem cell factor and transforming growth factor-β1. Using the enhanced growth characteristics of these MMC homologues, a novel limiting dilution assay for mast cell precursor (MCp) frequency has been developed. The assay is highly specific, in that cultures containing mast cells are identified with mMCP-1 specific antibody, and almost three-fold more sensitive than previously published systems. MCp frequencies were compared in BALB/c and C57/BL10 strains of mice that, respectively, respond rapidly and slowly to infection with T. spiralis. MCp frequency (1/378 bone marrow cells) was significantly greater (P<0.05) in BALB/c than C57/BL10 mice (frequency: 1/751). Similarly the rate of growth of MMC homologues and the production of mMCP-1 was significantly (P<0.05) greater in BALB/c than in C57/BL10 bone marrow cultures.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>12756069</pmid><doi>10.1079/JOH2002160</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Antibodies - analysis Bone Marrow Cells Cell Differentiation Cells, Cultured Chymases Culture Media Fluorescent Antibody Technique Interleukin-3 Interleukin-9 Intestinal Diseases, Parasitic - immunology Intestinal Mucosa - immunology Male Mast Cells - immunology Mice Mice, Inbred BALB C Mice, Inbred C57BL Serine Endopeptidases - immunology Species Specificity Stem Cell Factor Transforming Growth Factor beta Trichinella spiralis Trichinellosis - immunology |
title | Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited |
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