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...
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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 |
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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 < 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&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 < 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 < 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> |
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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 |
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