Gamma interferon cooperates with lipopolysaccharide to activate mouse splenic macrophages to an antihistoplasma state

Inhibition of the intracellular growth of Histoplasma capsulatum by murine resident red pulp splenic macrophages was examined. Splenic macrophages, unlike resident peritoneal macrophages, required a prolonged preincubation (18 h) with recombinant murine gamma interferon (rMuIFN-gamma) for activation...

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Veröffentlicht in:Infection and Immunity 1993-04, Vol.61 (4), p.1468-1473
Hauptverfasser: Lane, T.E, Wu-Hsieh, B.A, Howard, D.H
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Wu-Hsieh, B.A
Howard, D.H
description Inhibition of the intracellular growth of Histoplasma capsulatum by murine resident red pulp splenic macrophages was examined. Splenic macrophages, unlike resident peritoneal macrophages, required a prolonged preincubation (18 h) with recombinant murine gamma interferon (rMuIFN-gamma) for activation. To be fully activated, the splenic macrophages required incubation with rMuIFN-gamma in combination with 0.1 micrograms of lipopolysaccharide (LPS) per ml. Splenic macrophages stimulated with rMuIFN-gamma, LPS, or rMuIFN-gamma and LPS produced tumor necrosis factor alpha (TNF-alpha), but recombinant murine TNF-alpha (rMuTNF-alpha) did not activate macrophages when used alone or as a second signal with rMuIFN-gamma. Anti-TNF-alpha antibody did not block IFN-gamma-LPS activation of splenic macrophages to any significant extent. One hundred micromolar ferrous sulfate antagonized IFN-gamma-LPS activation of splenic macrophages, indicating that iron was involved in the fungistatic activity of cytokine-stimulated phagocytes. Our results indicate that (i) splenic macrophages differ significantly from peritoneal macrophages in their requirements for activation and (ii) the mechanism by which splenic macrophages exert their antifungal effects involves iron
doi_str_mv 10.1128/IAI.61.4.1468-1473.1993
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Splenic macrophages, unlike resident peritoneal macrophages, required a prolonged preincubation (18 h) with recombinant murine gamma interferon (rMuIFN-gamma) for activation. To be fully activated, the splenic macrophages required incubation with rMuIFN-gamma in combination with 0.1 micrograms of lipopolysaccharide (LPS) per ml. Splenic macrophages stimulated with rMuIFN-gamma, LPS, or rMuIFN-gamma and LPS produced tumor necrosis factor alpha (TNF-alpha), but recombinant murine TNF-alpha (rMuTNF-alpha) did not activate macrophages when used alone or as a second signal with rMuIFN-gamma. Anti-TNF-alpha antibody did not block IFN-gamma-LPS activation of splenic macrophages to any significant extent. One hundred micromolar ferrous sulfate antagonized IFN-gamma-LPS activation of splenic macrophages, indicating that iron was involved in the fungistatic activity of cytokine-stimulated phagocytes. 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Psychology ; Fundamental immunology ; HISTOPLASMA ; Histoplasma - immunology ; Histoplasmosis - immunology ; Immunobiology ; Interferon-gamma - administration &amp; dosage ; Iron - pharmacology ; Lipopolysaccharides - administration &amp; dosage ; Macrophage Activation - drug effects ; Macrophages - immunology ; Male ; Mice ; Mice, Inbred C57BL ; Monocytes, macrophages ; Myeloid cells: ontogeny, maturation, markers, receptors ; PHAGOCYTE ; RATON ; Recombinant Proteins ; SOURIS ; Spleen - cytology ; Spleen - immunology ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>Infection and Immunity, 1993-04, Vol.61 (4), p.1468-1473</ispartof><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-fd539b774222d83b5354147544d47d413053ab3ae0541682918ad24909fa8b7c3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC281387/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC281387/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4717725$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8454351$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lane, T.E</creatorcontrib><creatorcontrib>Wu-Hsieh, B.A</creatorcontrib><creatorcontrib>Howard, D.H</creatorcontrib><title>Gamma interferon cooperates with lipopolysaccharide to activate mouse splenic macrophages to an antihistoplasma state</title><title>Infection and Immunity</title><addtitle>Infect Immun</addtitle><description>Inhibition of the intracellular growth of Histoplasma capsulatum by murine resident red pulp splenic macrophages was examined. Splenic macrophages, unlike resident peritoneal macrophages, required a prolonged preincubation (18 h) with recombinant murine gamma interferon (rMuIFN-gamma) for activation. To be fully activated, the splenic macrophages required incubation with rMuIFN-gamma in combination with 0.1 micrograms of lipopolysaccharide (LPS) per ml. Splenic macrophages stimulated with rMuIFN-gamma, LPS, or rMuIFN-gamma and LPS produced tumor necrosis factor alpha (TNF-alpha), but recombinant murine TNF-alpha (rMuTNF-alpha) did not activate macrophages when used alone or as a second signal with rMuIFN-gamma. Anti-TNF-alpha antibody did not block IFN-gamma-LPS activation of splenic macrophages to any significant extent. One hundred micromolar ferrous sulfate antagonized IFN-gamma-LPS activation of splenic macrophages, indicating that iron was involved in the fungistatic activity of cytokine-stimulated phagocytes. 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Psychology</subject><subject>Fundamental immunology</subject><subject>HISTOPLASMA</subject><subject>Histoplasma - immunology</subject><subject>Histoplasmosis - immunology</subject><subject>Immunobiology</subject><subject>Interferon-gamma - administration &amp; dosage</subject><subject>Iron - pharmacology</subject><subject>Lipopolysaccharides - administration &amp; dosage</subject><subject>Macrophage Activation - drug effects</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Monocytes, macrophages</subject><subject>Myeloid cells: ontogeny, maturation, markers, receptors</subject><subject>PHAGOCYTE</subject><subject>RATON</subject><subject>Recombinant Proteins</subject><subject>SOURIS</subject><subject>Spleen - cytology</subject><subject>Spleen - immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0019-9567</issn><issn>1098-5522</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV-L1DAUxYso67j6BQSxgvjW2vxrkod9WBZdBxZ80H0Od9J0GmmbmmR22W_vLTMMLgRCcn_n3pycovhImpoQqr5ur7d1S2peE96qinDJaqI1e1FsSKNVJQSlL4tN0xBdadHK18WblP7gkXOuLooLxQVngmyKwy1ME5R-zi72Loa5tCEsLkJ2qXz0eShHv4QljE8JrB0g-s6VOZRgs39AqJzCIbkyLaObvS0nsDEsA-xRvVIzruwHn3JYRkg4KWVUvS1e9TAm9-60Xxb337_9vvlR3f283d5c31VWyCZXfSeY3knJKaWdYjvBBEergvOOy44T1ggGOwauwftWUU0UdJTrRvegdtKyy-Lq2Hc57CbXWTfnCKNZop8gPpkA3jyvzH4w-_BgqCJMSdR_Oelj-HtwKZvJJ-vGEWaHvg1pmRCSagTlEUT7KUXXn2eQxqyBGY-zWmK4WQMza2BmDQyVH_5_4ll3Sgjrn091SBbGPsJsfTpjXBIpqUDs0xEb_H549NEZ_O3nQ5F5f2R6CAb2Edvc_9KcoNGW_QMuvLVt</recordid><startdate>19930401</startdate><enddate>19930401</enddate><creator>Lane, T.E</creator><creator>Wu-Hsieh, B.A</creator><creator>Howard, D.H</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>7T5</scope><scope>H94</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>19930401</creationdate><title>Gamma interferon cooperates with lipopolysaccharide to activate mouse splenic macrophages to an antihistoplasma state</title><author>Lane, T.E ; Wu-Hsieh, B.A ; Howard, D.H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-fd539b774222d83b5354147544d47d413053ab3ae0541682918ad24909fa8b7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Drug Synergism</topic><topic>FAGOCITOS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>HISTOPLASMA</topic><topic>Histoplasma - immunology</topic><topic>Histoplasmosis - immunology</topic><topic>Immunobiology</topic><topic>Interferon-gamma - administration &amp; dosage</topic><topic>Iron - pharmacology</topic><topic>Lipopolysaccharides - administration &amp; dosage</topic><topic>Macrophage Activation - drug effects</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Monocytes, macrophages</topic><topic>Myeloid cells: ontogeny, maturation, markers, receptors</topic><topic>PHAGOCYTE</topic><topic>RATON</topic><topic>Recombinant Proteins</topic><topic>SOURIS</topic><topic>Spleen - cytology</topic><topic>Spleen - immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lane, T.E</creatorcontrib><creatorcontrib>Wu-Hsieh, B.A</creatorcontrib><creatorcontrib>Howard, D.H</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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</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>Lane, T.E</au><au>Wu-Hsieh, B.A</au><au>Howard, D.H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gamma interferon cooperates with lipopolysaccharide to activate mouse splenic macrophages to an antihistoplasma state</atitle><jtitle>Infection and Immunity</jtitle><addtitle>Infect Immun</addtitle><date>1993-04-01</date><risdate>1993</risdate><volume>61</volume><issue>4</issue><spage>1468</spage><epage>1473</epage><pages>1468-1473</pages><issn>0019-9567</issn><eissn>1098-5522</eissn><coden>INFIBR</coden><abstract>Inhibition of the intracellular growth of Histoplasma capsulatum by murine resident red pulp splenic macrophages was examined. Splenic macrophages, unlike resident peritoneal macrophages, required a prolonged preincubation (18 h) with recombinant murine gamma interferon (rMuIFN-gamma) for activation. To be fully activated, the splenic macrophages required incubation with rMuIFN-gamma in combination with 0.1 micrograms of lipopolysaccharide (LPS) per ml. Splenic macrophages stimulated with rMuIFN-gamma, LPS, or rMuIFN-gamma and LPS produced tumor necrosis factor alpha (TNF-alpha), but recombinant murine TNF-alpha (rMuTNF-alpha) did not activate macrophages when used alone or as a second signal with rMuIFN-gamma. Anti-TNF-alpha antibody did not block IFN-gamma-LPS activation of splenic macrophages to any significant extent. One hundred micromolar ferrous sulfate antagonized IFN-gamma-LPS activation of splenic macrophages, indicating that iron was involved in the fungistatic activity of cytokine-stimulated phagocytes. 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source American Society for Microbiology; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Animals
Biological and medical sciences
Drug Synergism
FAGOCITOS
Fundamental and applied biological sciences. Psychology
Fundamental immunology
HISTOPLASMA
Histoplasma - immunology
Histoplasmosis - immunology
Immunobiology
Interferon-gamma - administration & dosage
Iron - pharmacology
Lipopolysaccharides - administration & dosage
Macrophage Activation - drug effects
Macrophages - immunology
Male
Mice
Mice, Inbred C57BL
Monocytes, macrophages
Myeloid cells: ontogeny, maturation, markers, receptors
PHAGOCYTE
RATON
Recombinant Proteins
SOURIS
Spleen - cytology
Spleen - immunology
Tumor Necrosis Factor-alpha - metabolism
title Gamma interferon cooperates with lipopolysaccharide to activate mouse splenic macrophages to an antihistoplasma state
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