Loading…

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....

Full description

Saved in:
Bibliographic Details
Published in:Journal of helminthology 2003-06, Vol.77 (2), p.155-161
Main Authors: Brown, J.K., Wright, S.H., Miller, H.R.P.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683
cites cdi_FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683
container_end_page 161
container_issue 2
container_start_page 155
container_title Journal of helminthology
container_volume 77
creator Brown, J.K.
Wright, S.H.
Miller, H.R.P.
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_73296177</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cupid>10_1079_JOH2002160</cupid><sourcerecordid>73296177</sourcerecordid><originalsourceid>FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683</originalsourceid><addsrcrecordid>eNpt0V1rFDEUBuAgFru23vgDJHjhhTiak8-md1rsVt1aBAXxJmQyJ5K6M7NNZsT--6bs4oJ4FUge3vOSQ8hTYK-BGfvm49UFZ4yDZg_IAqRRDdfWPCSLeskbkPb7IXlcyjVjTABXj8ghcKM003ZBbi7nMBa_pr0vEw24Xhfqh44O2Ptp7JCmIWKY0jic0jJln4ambDCkmALtUoyYcQhYKtsn0E3GMOcyZhoz3sxV3NKMv1NJE3bH5CD6dcEnu_OIfDt___XsolldLT-cvV01QSqYGhFbr7HVCJbFTlkrIChxEiDqVhqpZRtMDCoIqQUIrWVUXAUFnQLopD4RR-TFNneTx9qhTK5P5b6eH3CcizOCWw3GVPj8H3g9znmo3RwHIa2RSlf0cotCHkvJGN0mp97nWwfM3W_B7bdQ8bNd4tz22O3p7tsraLYglQn__H33-ZfTRhjl9PKLs-erH8t3nz85Uf2r3XTftzl1P3Hf8T_z7wBpTp-m</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213497456</pqid></control><display><type>article</type><title>Mucosal mast cells and nematode infection: strain-specific differences in mast cell precursor frequency revisited</title><source>Cambridge University Press</source><creator>Brown, J.K. ; Wright, S.H. ; Miller, H.R.P.</creator><creatorcontrib>Brown, J.K. ; Wright, S.H. ; Miller, H.R.P.</creatorcontrib><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&lt;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&lt;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&lt;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&lt;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 &amp; 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 &amp; 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 &amp; Fisheries Abstracts (ASFA) 1: Biological Sciences &amp; Living Resources</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Aquatic Science &amp; Fisheries Abstracts (ASFA) Professional</collection><collection>Agriculture Science Database</collection><collection>Health &amp; 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&lt;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&lt;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>
fulltext fulltext
identifier ISSN: 0022-149X
ispartof Journal of helminthology, 2003-06, Vol.77 (2), p.155-161
issn 0022-149X
1475-2697
language eng
recordid cdi_proquest_miscellaneous_73296177
source Cambridge University Press
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T12%3A03%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mucosal%20mast%20cells%20and%20nematode%20infection:%20strain-specific%20differences%20in%20mast%20cell%20precursor%20frequency%20revisited&rft.jtitle=Journal%20of%20helminthology&rft.au=Brown,%20J.K.&rft.date=2003-06&rft.volume=77&rft.issue=2&rft.spage=155&rft.epage=161&rft.pages=155-161&rft.issn=0022-149X&rft.eissn=1475-2697&rft_id=info:doi/10.1079/JOH2002160&rft_dat=%3Cproquest_cross%3E73296177%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c451t-3fba6eb6e190fd59931c538c1f6b47464bc7fc5c346313664f525c51d511d4683%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=213497456&rft_id=info:pmid/12756069&rft_cupid=10_1079_JOH2002160&rfr_iscdi=true