biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha

Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Infection and immunity 1998-09, Vol.66 (9), p.4087-4092
Hauptverfasser: Lafleur, R.L, Abrahamsen, M.S, Maheswaran, S.K
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4092
container_issue 9
container_start_page 4087
container_title Infection and immunity
container_volume 66
creator Lafleur, R.L
Abrahamsen, M.S
Maheswaran, S.K
description Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the pathological hallmarks of bovine pneumonic pasteurellosis is an influx of neutrophils into the alveolar spaces. This pronounced influx suggests the local production of a chematactic factor(s) such as interleulcin-8 (IL-8). In the context of the lung, the alveolar macrophage appears to be the major producer of IL-8, a proinflammatory cytokine with potent neutrophil chemotactic activity. By using Northern blot analysis, we have examined the kinetics of IL-8 mRNA expression in P. haemolytica LPS-stimulated bovine alveolar macrophages and found that 1 ng of LPS per ml induces maximal expression of IL-8 mRNA. The results also indicate a biphasic time course expression pattern in which IL-8 mRNA levels peak between 1 and 2 h in the first phase and between 16 and 24 h in the second phase (P < 0.01). In addition, monospecific polyclonal antibodies were used to demonstrate the role of tumor necrosis factor alpha (TN F-alpha) in the second phase of IL-8 mRNA expression. Our findings support a role for P. haemolytica LPS and TN F-alpha in the induction of IL-8 from bovine alveolar macrophages.
doi_str_mv 10.1128/iai.66.9.4087-4092.1998
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_108490</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>16506117</sourcerecordid><originalsourceid>FETCH-LOGICAL-c446t-82b11033d9ec0c4dc5992b74d4788b433f672d76d595183bd82785d50dc4f8943</originalsourceid><addsrcrecordid>eNpVkd-O1CAYxRujWcfVRzDLhfGuI1Ba4MKLycY_k2zUqHtNvgKdQWmpQCfOi_l8MpnJRq_I4fwOH3Cq6obgNSFUvHHg1l23lmuGBa8ZlnRNpBSPqhXBUtRtS-njaoUxkbVsO_60epbSjyIZY-KqupKcUN7SVfWnd_MektNo_Pppg-zvOdqUXJjQDDnbOKEwoD4c3GSRm8qGt8tPN9WiKPQFUrZLtN4D2oMdgz9mpwF5N4e5iARa7yE6Y-uU3bh4yNYg8AcbPEQ0go6hTN_ZhFxCc3Rjgf0RmcWiHFBexhDRZAuVij-AzkWDL5Hn1ZMBfLIvLut1df_-3ffbj_Xd5w_b281drRnrci1oTwhuGiOtxpoZ3UpJe84M40L0rGmGjlPDO9PKloimN4Jy0ZoWG80GIVlzXb09nzsv_WiNtlOO4NX5qkcVwKn_ncnt1S4cFMGCSVzyry_5GH4tNmU1uqRPHzbZsCRFuhZ3hPAC8jN4emyKdniYQbA6Na62m63qOiXVqXF1alydGi_Jl_9e8SF3qbj4ry4-JA1-iDBplx4wykiHuSzYzRkbICjYxYLcf6OYNJhKTIQQzV8f28R1</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16506117</pqid></control><display><type>article</type><title>biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha</title><source>American Society for Microbiology</source><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Lafleur, R.L ; Abrahamsen, M.S ; Maheswaran, S.K</creator><contributor>McGhee, J. R.</contributor><creatorcontrib>Lafleur, R.L ; Abrahamsen, M.S ; Maheswaran, S.K ; McGhee, J. R.</creatorcontrib><description>Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the pathological hallmarks of bovine pneumonic pasteurellosis is an influx of neutrophils into the alveolar spaces. This pronounced influx suggests the local production of a chematactic factor(s) such as interleulcin-8 (IL-8). In the context of the lung, the alveolar macrophage appears to be the major producer of IL-8, a proinflammatory cytokine with potent neutrophil chemotactic activity. By using Northern blot analysis, we have examined the kinetics of IL-8 mRNA expression in P. haemolytica LPS-stimulated bovine alveolar macrophages and found that 1 ng of LPS per ml induces maximal expression of IL-8 mRNA. The results also indicate a biphasic time course expression pattern in which IL-8 mRNA levels peak between 1 and 2 h in the first phase and between 16 and 24 h in the second phase (P &lt; 0.01). In addition, monospecific polyclonal antibodies were used to demonstrate the role of tumor necrosis factor alpha (TN F-alpha) in the second phase of IL-8 mRNA expression. Our findings support a role for P. haemolytica LPS and TN F-alpha in the induction of IL-8 from bovine alveolar macrophages.</description><identifier>ISSN: 0019-9567</identifier><identifier>EISSN: 1098-5522</identifier><identifier>DOI: 10.1128/iai.66.9.4087-4092.1998</identifier><identifier>PMID: 9712752</identifier><identifier>CODEN: INFIBR</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Animals ; Antibodies - metabolism ; Bacteriology ; Biological and medical sciences ; Cattle ; Cloning, Molecular ; DNA, Complementary ; Fundamental and applied biological sciences. Psychology ; gene expression ; Gene Expression Regulation - drug effects ; Host Response and Inflammation ; Humans ; Interleukin-8 - genetics ; Kinetics ; Lipopolysaccharides - immunology ; Lipopolysaccharides - pharmacology ; Macrophages, Alveolar - drug effects ; Macrophages, Alveolar - immunology ; Mannheimia haemolytica - immunology ; messenger RNA ; Microbiology ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Recombinant Proteins - pharmacology ; RNA, Messenger ; Tumor Necrosis Factor-alpha - genetics ; Tumor Necrosis Factor-alpha - immunology ; Tumor Necrosis Factor-alpha - metabolism ; Tumor Necrosis Factor-alpha - pharmacology</subject><ispartof>Infection and immunity, 1998-09, Vol.66 (9), p.4087-4092</ispartof><rights>1998 INIST-CNRS</rights><rights>Copyright © 1998, American Society for Microbiology 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-82b11033d9ec0c4dc5992b74d4788b433f672d76d595183bd82785d50dc4f8943</citedby><cites>FETCH-LOGICAL-c446t-82b11033d9ec0c4dc5992b74d4788b433f672d76d595183bd82785d50dc4f8943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC108490/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC108490/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,3189,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2416079$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9712752$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>McGhee, J. R.</contributor><creatorcontrib>Lafleur, R.L</creatorcontrib><creatorcontrib>Abrahamsen, M.S</creatorcontrib><creatorcontrib>Maheswaran, S.K</creatorcontrib><title>biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha</title><title>Infection and immunity</title><addtitle>Infect Immun</addtitle><description>Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the pathological hallmarks of bovine pneumonic pasteurellosis is an influx of neutrophils into the alveolar spaces. This pronounced influx suggests the local production of a chematactic factor(s) such as interleulcin-8 (IL-8). In the context of the lung, the alveolar macrophage appears to be the major producer of IL-8, a proinflammatory cytokine with potent neutrophil chemotactic activity. By using Northern blot analysis, we have examined the kinetics of IL-8 mRNA expression in P. haemolytica LPS-stimulated bovine alveolar macrophages and found that 1 ng of LPS per ml induces maximal expression of IL-8 mRNA. The results also indicate a biphasic time course expression pattern in which IL-8 mRNA levels peak between 1 and 2 h in the first phase and between 16 and 24 h in the second phase (P &lt; 0.01). In addition, monospecific polyclonal antibodies were used to demonstrate the role of tumor necrosis factor alpha (TN F-alpha) in the second phase of IL-8 mRNA expression. Our findings support a role for P. haemolytica LPS and TN F-alpha in the induction of IL-8 from bovine alveolar macrophages.</description><subject>Animals</subject><subject>Antibodies - metabolism</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Cattle</subject><subject>Cloning, Molecular</subject><subject>DNA, Complementary</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gene expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Host Response and Inflammation</subject><subject>Humans</subject><subject>Interleukin-8 - genetics</subject><subject>Kinetics</subject><subject>Lipopolysaccharides - immunology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages, Alveolar - drug effects</subject><subject>Macrophages, Alveolar - immunology</subject><subject>Mannheimia haemolytica - immunology</subject><subject>messenger RNA</subject><subject>Microbiology</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Recombinant Proteins - pharmacology</subject><subject>RNA, Messenger</subject><subject>Tumor Necrosis Factor-alpha - genetics</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Tumor Necrosis Factor-alpha - pharmacology</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkd-O1CAYxRujWcfVRzDLhfGuI1Ba4MKLycY_k2zUqHtNvgKdQWmpQCfOi_l8MpnJRq_I4fwOH3Cq6obgNSFUvHHg1l23lmuGBa8ZlnRNpBSPqhXBUtRtS-njaoUxkbVsO_60epbSjyIZY-KqupKcUN7SVfWnd_MektNo_Pppg-zvOdqUXJjQDDnbOKEwoD4c3GSRm8qGt8tPN9WiKPQFUrZLtN4D2oMdgz9mpwF5N4e5iARa7yE6Y-uU3bh4yNYg8AcbPEQ0go6hTN_ZhFxCc3Rjgf0RmcWiHFBexhDRZAuVij-AzkWDL5Hn1ZMBfLIvLut1df_-3ffbj_Xd5w_b281drRnrci1oTwhuGiOtxpoZ3UpJe84M40L0rGmGjlPDO9PKloimN4Jy0ZoWG80GIVlzXb09nzsv_WiNtlOO4NX5qkcVwKn_ncnt1S4cFMGCSVzyry_5GH4tNmU1uqRPHzbZsCRFuhZ3hPAC8jN4emyKdniYQbA6Na62m63qOiXVqXF1alydGi_Jl_9e8SF3qbj4ry4-JA1-iDBplx4wykiHuSzYzRkbICjYxYLcf6OYNJhKTIQQzV8f28R1</recordid><startdate>19980901</startdate><enddate>19980901</enddate><creator>Lafleur, R.L</creator><creator>Abrahamsen, M.S</creator><creator>Maheswaran, S.K</creator><general>American Society for Microbiology</general><scope>FBQ</scope><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><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>19980901</creationdate><title>biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha</title><author>Lafleur, R.L ; Abrahamsen, M.S ; Maheswaran, S.K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-82b11033d9ec0c4dc5992b74d4788b433f672d76d595183bd82785d50dc4f8943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antibodies - metabolism</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Cattle</topic><topic>Cloning, Molecular</topic><topic>DNA, Complementary</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gene expression</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Host Response and Inflammation</topic><topic>Humans</topic><topic>Interleukin-8 - genetics</topic><topic>Kinetics</topic><topic>Lipopolysaccharides - immunology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages, Alveolar - drug effects</topic><topic>Macrophages, Alveolar - immunology</topic><topic>Mannheimia haemolytica - immunology</topic><topic>messenger RNA</topic><topic>Microbiology</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Recombinant Proteins - pharmacology</topic><topic>RNA, Messenger</topic><topic>Tumor Necrosis Factor-alpha - genetics</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Tumor Necrosis Factor-alpha - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lafleur, R.L</creatorcontrib><creatorcontrib>Abrahamsen, M.S</creatorcontrib><creatorcontrib>Maheswaran, S.K</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Infection and immunity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lafleur, R.L</au><au>Abrahamsen, M.S</au><au>Maheswaran, S.K</au><au>McGhee, J. R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha</atitle><jtitle>Infection and immunity</jtitle><addtitle>Infect Immun</addtitle><date>1998-09-01</date><risdate>1998</risdate><volume>66</volume><issue>9</issue><spage>4087</spage><epage>4092</epage><pages>4087-4092</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Pasteurella haemolytica serotype 1 is the bacterial agent responsible for the pathophysiological events associated with bovine pneumonic pasteurellosis. Our previous studies support a role for the lipopolysaccharide (LPS) from P. haemolytica in the induction of proinflammatory cytokines. One of the pathological hallmarks of bovine pneumonic pasteurellosis is an influx of neutrophils into the alveolar spaces. This pronounced influx suggests the local production of a chematactic factor(s) such as interleulcin-8 (IL-8). In the context of the lung, the alveolar macrophage appears to be the major producer of IL-8, a proinflammatory cytokine with potent neutrophil chemotactic activity. By using Northern blot analysis, we have examined the kinetics of IL-8 mRNA expression in P. haemolytica LPS-stimulated bovine alveolar macrophages and found that 1 ng of LPS per ml induces maximal expression of IL-8 mRNA. The results also indicate a biphasic time course expression pattern in which IL-8 mRNA levels peak between 1 and 2 h in the first phase and between 16 and 24 h in the second phase (P &lt; 0.01). In addition, monospecific polyclonal antibodies were used to demonstrate the role of tumor necrosis factor alpha (TN F-alpha) in the second phase of IL-8 mRNA expression. Our findings support a role for P. haemolytica LPS and TN F-alpha in the induction of IL-8 from bovine alveolar macrophages.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>9712752</pmid><doi>10.1128/iai.66.9.4087-4092.1998</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0019-9567
ispartof Infection and immunity, 1998-09, Vol.66 (9), p.4087-4092
issn 0019-9567
1098-5522
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_108490
source American Society for Microbiology; MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Animals
Antibodies - metabolism
Bacteriology
Biological and medical sciences
Cattle
Cloning, Molecular
DNA, Complementary
Fundamental and applied biological sciences. Psychology
gene expression
Gene Expression Regulation - drug effects
Host Response and Inflammation
Humans
Interleukin-8 - genetics
Kinetics
Lipopolysaccharides - immunology
Lipopolysaccharides - pharmacology
Macrophages, Alveolar - drug effects
Macrophages, Alveolar - immunology
Mannheimia haemolytica - immunology
messenger RNA
Microbiology
Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains
Recombinant Proteins - pharmacology
RNA, Messenger
Tumor Necrosis Factor-alpha - genetics
Tumor Necrosis Factor-alpha - immunology
Tumor Necrosis Factor-alpha - metabolism
Tumor Necrosis Factor-alpha - pharmacology
title biphasic mRNA expression pattern of bovine interleukin-8 in Pasteurella haemolytica lipopolysaccharide-stimulated alveolar macrophages is primarily due to tumor necrosis factor alpha
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-12T09%3A34%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=biphasic%20mRNA%20expression%20pattern%20of%20bovine%20interleukin-8%20in%20Pasteurella%20haemolytica%20lipopolysaccharide-stimulated%20alveolar%20macrophages%20is%20primarily%20due%20to%20tumor%20necrosis%20factor%20alpha&rft.jtitle=Infection%20and%20immunity&rft.au=Lafleur,%20R.L&rft.date=1998-09-01&rft.volume=66&rft.issue=9&rft.spage=4087&rft.epage=4092&rft.pages=4087-4092&rft.issn=0019-9567&rft.eissn=1098-5522&rft.coden=INFIBR&rft_id=info:doi/10.1128/iai.66.9.4087-4092.1998&rft_dat=%3Cproquest_pubme%3E16506117%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16506117&rft_id=info:pmid/9712752&rfr_iscdi=true