Loading…

Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation

Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9, on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and s...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of immunology (1950) 2008-07, Vol.181 (2), p.1307-1314
Main Authors: Glant, Tibor T, Szanto, Sandor, Vegvari, Aniko, Szabo, Zoltan, Kis-Toth, Katalin, Mikecz, Katalin, Adarichev, Vyacheslav A
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-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3
cites cdi_FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3
container_end_page 1314
container_issue 2
container_start_page 1307
container_title The Journal of immunology (1950)
container_volume 181
creator Glant, Tibor T
Szanto, Sandor
Vegvari, Aniko
Szabo, Zoltan
Kis-Toth, Katalin
Mikecz, Katalin
Adarichev, Vyacheslav A
description Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9, on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and separately each of the two loci of DBA/2 arthritis-resistant origin in susceptible BALB/c background confirmed locations of two loci on chr15: the major Pgia9 and lesser Pgia8 locus. Distal part of chr15 (Pgia9) showed a major suppressive effect on PGIA susceptibility in females (40%, p < 0.001), whereas the effect of this locus in congenic males was still significant but weaker. Proximal part of chr15 (Pgia8) demonstrated mild and transient effect upon arthritis; this effect was PGIA-promoting in males and suppressive in females. Pgia8 and Pgia9 loci demonstrated an additive mode of inheritance, since when they were both incorporated in consomic chr15 strain, the total effect was a sum of the two loci. Using F(2) population of the intercross of wild-type and chr15 consomic strain, we confirmed and refined quantitative trait locus positions and identified a strong correlation between disease susceptibility and lymphocyte-producing cytokines of TNF-alpha and IL-6. Both Pgia8 and Pgia9 loci on chr15 appear to control IL-6 production in spleen cultures of arthritic mice, providing an important link to the mechanism of autoimmune inflammation.
doi_str_mv 10.4049/jimmunol.181.2.1307
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69303490</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20930548</sourcerecordid><originalsourceid>FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3</originalsourceid><addsrcrecordid>eNqFkd2K1DAYhoMo7rh6BYLkSI865q9perjMrjpQUGQ9Dmn7dZolacakpc41eNNmnRE98-iFj-d9A3kQek3JVhBRv3-w3i9TcFuq6JZtKSfVE7ShZUkKKYl8ijaEMFbQSlZX6EVKD4QQSZh4jq6oyoBU5Qb9vF8DbkJncZjwbozBhxQ8YFriXZjmGBy--3GEaD1Ms3HuhPdTv3TQ45s4j9HONuGcYTmMOQHf2mGAmFlrHP4Kh8WZ2ebpMOB9U0hsph43J38cQ3eaAX_JD9hc-A29RM8G4xK8uuQ1-vbh7n73qWg-f9zvbpqiE5TORW9MXxFeSqOAyVqINh94bSilhNOSlQOtWNsaOrRcdaVSreyFqioBhoBhHb9Gb8-7xxi-L5Bm7W3qwDkzQViSljUnXNTkvyAjmSyFyiA_g10MKUUY9DH_mIknTYl-lKX_yNJZlmb6UVZuvbnML62H_m_nYicD787AaA_jaiPo5LODjFO9rus_U78AHf6h3Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20930548</pqid></control><display><type>article</type><title>Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation</title><source>EZB Free E-Journals</source><creator>Glant, Tibor T ; Szanto, Sandor ; Vegvari, Aniko ; Szabo, Zoltan ; Kis-Toth, Katalin ; Mikecz, Katalin ; Adarichev, Vyacheslav A</creator><creatorcontrib>Glant, Tibor T ; Szanto, Sandor ; Vegvari, Aniko ; Szabo, Zoltan ; Kis-Toth, Katalin ; Mikecz, Katalin ; Adarichev, Vyacheslav A</creatorcontrib><description>Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9, on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and separately each of the two loci of DBA/2 arthritis-resistant origin in susceptible BALB/c background confirmed locations of two loci on chr15: the major Pgia9 and lesser Pgia8 locus. Distal part of chr15 (Pgia9) showed a major suppressive effect on PGIA susceptibility in females (40%, p &lt; 0.001), whereas the effect of this locus in congenic males was still significant but weaker. Proximal part of chr15 (Pgia8) demonstrated mild and transient effect upon arthritis; this effect was PGIA-promoting in males and suppressive in females. Pgia8 and Pgia9 loci demonstrated an additive mode of inheritance, since when they were both incorporated in consomic chr15 strain, the total effect was a sum of the two loci. Using F(2) population of the intercross of wild-type and chr15 consomic strain, we confirmed and refined quantitative trait locus positions and identified a strong correlation between disease susceptibility and lymphocyte-producing cytokines of TNF-alpha and IL-6. Both Pgia8 and Pgia9 loci on chr15 appear to control IL-6 production in spleen cultures of arthritic mice, providing an important link to the mechanism of autoimmune inflammation.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.181.2.1307</identifier><identifier>PMID: 18606685</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Animals ; Arthritis, Experimental - genetics ; Arthritis, Experimental - immunology ; Cell Proliferation ; Chromosomes, Mammalian - genetics ; Female ; Genetic Predisposition to Disease ; Humans ; Interleukin-6 - immunology ; Interleukin-6 - metabolism ; Lymphocyte Activation ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Inbred DBA ; Proteoglycans - immunology ; Quantitative Trait Loci ; Tumor Necrosis Factor-alpha - immunology ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>The Journal of immunology (1950), 2008-07, Vol.181 (2), p.1307-1314</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3</citedby><cites>FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18606685$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Glant, Tibor T</creatorcontrib><creatorcontrib>Szanto, Sandor</creatorcontrib><creatorcontrib>Vegvari, Aniko</creatorcontrib><creatorcontrib>Szabo, Zoltan</creatorcontrib><creatorcontrib>Kis-Toth, Katalin</creatorcontrib><creatorcontrib>Mikecz, Katalin</creatorcontrib><creatorcontrib>Adarichev, Vyacheslav A</creatorcontrib><title>Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9, on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and separately each of the two loci of DBA/2 arthritis-resistant origin in susceptible BALB/c background confirmed locations of two loci on chr15: the major Pgia9 and lesser Pgia8 locus. Distal part of chr15 (Pgia9) showed a major suppressive effect on PGIA susceptibility in females (40%, p &lt; 0.001), whereas the effect of this locus in congenic males was still significant but weaker. Proximal part of chr15 (Pgia8) demonstrated mild and transient effect upon arthritis; this effect was PGIA-promoting in males and suppressive in females. Pgia8 and Pgia9 loci demonstrated an additive mode of inheritance, since when they were both incorporated in consomic chr15 strain, the total effect was a sum of the two loci. Using F(2) population of the intercross of wild-type and chr15 consomic strain, we confirmed and refined quantitative trait locus positions and identified a strong correlation between disease susceptibility and lymphocyte-producing cytokines of TNF-alpha and IL-6. Both Pgia8 and Pgia9 loci on chr15 appear to control IL-6 production in spleen cultures of arthritic mice, providing an important link to the mechanism of autoimmune inflammation.</description><subject>Animals</subject><subject>Arthritis, Experimental - genetics</subject><subject>Arthritis, Experimental - immunology</subject><subject>Cell Proliferation</subject><subject>Chromosomes, Mammalian - genetics</subject><subject>Female</subject><subject>Genetic Predisposition to Disease</subject><subject>Humans</subject><subject>Interleukin-6 - immunology</subject><subject>Interleukin-6 - metabolism</subject><subject>Lymphocyte Activation</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred DBA</subject><subject>Proteoglycans - immunology</subject><subject>Quantitative Trait Loci</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkd2K1DAYhoMo7rh6BYLkSI865q9perjMrjpQUGQ9Dmn7dZolacakpc41eNNmnRE98-iFj-d9A3kQek3JVhBRv3-w3i9TcFuq6JZtKSfVE7ShZUkKKYl8ijaEMFbQSlZX6EVKD4QQSZh4jq6oyoBU5Qb9vF8DbkJncZjwbozBhxQ8YFriXZjmGBy--3GEaD1Ms3HuhPdTv3TQ45s4j9HONuGcYTmMOQHf2mGAmFlrHP4Kh8WZ2ebpMOB9U0hsph43J38cQ3eaAX_JD9hc-A29RM8G4xK8uuQ1-vbh7n73qWg-f9zvbpqiE5TORW9MXxFeSqOAyVqINh94bSilhNOSlQOtWNsaOrRcdaVSreyFqioBhoBhHb9Gb8-7xxi-L5Bm7W3qwDkzQViSljUnXNTkvyAjmSyFyiA_g10MKUUY9DH_mIknTYl-lKX_yNJZlmb6UVZuvbnML62H_m_nYicD787AaA_jaiPo5LODjFO9rus_U78AHf6h3Q</recordid><startdate>20080715</startdate><enddate>20080715</enddate><creator>Glant, Tibor T</creator><creator>Szanto, Sandor</creator><creator>Vegvari, Aniko</creator><creator>Szabo, Zoltan</creator><creator>Kis-Toth, Katalin</creator><creator>Mikecz, Katalin</creator><creator>Adarichev, Vyacheslav A</creator><general>Am Assoc Immnol</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>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20080715</creationdate><title>Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation</title><author>Glant, Tibor T ; Szanto, Sandor ; Vegvari, Aniko ; Szabo, Zoltan ; Kis-Toth, Katalin ; Mikecz, Katalin ; Adarichev, Vyacheslav A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Arthritis, Experimental - genetics</topic><topic>Arthritis, Experimental - immunology</topic><topic>Cell Proliferation</topic><topic>Chromosomes, Mammalian - genetics</topic><topic>Female</topic><topic>Genetic Predisposition to Disease</topic><topic>Humans</topic><topic>Interleukin-6 - immunology</topic><topic>Interleukin-6 - metabolism</topic><topic>Lymphocyte Activation</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred DBA</topic><topic>Proteoglycans - immunology</topic><topic>Quantitative Trait Loci</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glant, Tibor T</creatorcontrib><creatorcontrib>Szanto, Sandor</creatorcontrib><creatorcontrib>Vegvari, Aniko</creatorcontrib><creatorcontrib>Szabo, Zoltan</creatorcontrib><creatorcontrib>Kis-Toth, Katalin</creatorcontrib><creatorcontrib>Mikecz, Katalin</creatorcontrib><creatorcontrib>Adarichev, Vyacheslav A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Glant, Tibor T</au><au>Szanto, Sandor</au><au>Vegvari, Aniko</au><au>Szabo, Zoltan</au><au>Kis-Toth, Katalin</au><au>Mikecz, Katalin</au><au>Adarichev, Vyacheslav A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2008-07-15</date><risdate>2008</risdate><volume>181</volume><issue>2</issue><spage>1307</spage><epage>1314</epage><pages>1307-1314</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Using genetic linkage analysis of proteoglycan-induced arthritis (PGIA), a murine model for rheumatoid arthritis, we identified two loci, Pgia8 and Pgia9, on chromosome 15 (chr15) that appear to be implicated in disease susceptibility. Immunization of congenic strains carrying the entire chr15 and separately each of the two loci of DBA/2 arthritis-resistant origin in susceptible BALB/c background confirmed locations of two loci on chr15: the major Pgia9 and lesser Pgia8 locus. Distal part of chr15 (Pgia9) showed a major suppressive effect on PGIA susceptibility in females (40%, p &lt; 0.001), whereas the effect of this locus in congenic males was still significant but weaker. Proximal part of chr15 (Pgia8) demonstrated mild and transient effect upon arthritis; this effect was PGIA-promoting in males and suppressive in females. Pgia8 and Pgia9 loci demonstrated an additive mode of inheritance, since when they were both incorporated in consomic chr15 strain, the total effect was a sum of the two loci. Using F(2) population of the intercross of wild-type and chr15 consomic strain, we confirmed and refined quantitative trait locus positions and identified a strong correlation between disease susceptibility and lymphocyte-producing cytokines of TNF-alpha and IL-6. Both Pgia8 and Pgia9 loci on chr15 appear to control IL-6 production in spleen cultures of arthritic mice, providing an important link to the mechanism of autoimmune inflammation.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>18606685</pmid><doi>10.4049/jimmunol.181.2.1307</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-1767
ispartof The Journal of immunology (1950), 2008-07, Vol.181 (2), p.1307-1314
issn 0022-1767
1550-6606
language eng
recordid cdi_proquest_miscellaneous_69303490
source EZB Free E-Journals
subjects Animals
Arthritis, Experimental - genetics
Arthritis, Experimental - immunology
Cell Proliferation
Chromosomes, Mammalian - genetics
Female
Genetic Predisposition to Disease
Humans
Interleukin-6 - immunology
Interleukin-6 - metabolism
Lymphocyte Activation
Male
Mice
Mice, Inbred BALB C
Mice, Inbred DBA
Proteoglycans - immunology
Quantitative Trait Loci
Tumor Necrosis Factor-alpha - immunology
Tumor Necrosis Factor-alpha - metabolism
title Two Loci on Chromosome 15 Control Experimentally Induced Arthritis through the Differential Regulation of IL-6 and Lymphocyte Proliferation
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A01%3A06IST&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=Two%20Loci%20on%20Chromosome%2015%20Control%20Experimentally%20Induced%20Arthritis%20through%20the%20Differential%20Regulation%20of%20IL-6%20and%20Lymphocyte%20Proliferation&rft.jtitle=The%20Journal%20of%20immunology%20(1950)&rft.au=Glant,%20Tibor%20T&rft.date=2008-07-15&rft.volume=181&rft.issue=2&rft.spage=1307&rft.epage=1314&rft.pages=1307-1314&rft.issn=0022-1767&rft.eissn=1550-6606&rft_id=info:doi/10.4049/jimmunol.181.2.1307&rft_dat=%3Cproquest_cross%3E20930548%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c411t-daad70356a8e26944baad39a111031525f172bba1fb38c588b6d48774ea0ea2c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=20930548&rft_id=info:pmid/18606685&rfr_iscdi=true