Defensins: natural peptide antibiotics of human neutrophils
We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-...
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Veröffentlicht in: | The Journal of clinical investigation 1985-10, Vol.76 (4), p.1427-1435 |
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description | We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-3, and which will be referred to as "defensins." HNP 1-3, a mixture of the three defensins, killed Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli effectively in vitro when tested in 10 mM phosphate buffer containing certain nutrients, but it had little or no bactericidal activity in nutrient-free buffer. In contrast, the nutrient-free buffer supported a high degree of activity by HNP 1-3 against Cryptococcus neoformans. In addition to its antibacterial and antifungal properties, HNP 1-3 directly inactivated herpes simplex virus, Type 1. Two of the individual purified defensins, HNP-1 and HNP-2, were as microbicidal as the mixture HNP 1-3. HNP-3 was less active than the other defensins against most but not all of the microbes tested. Immunoperoxidase stains revealed HNP 1-3 to have a granular localization in the neutrophil's cytoplasm by light microscopy. Frozen thin section immunogold transmission electron microscopy showed HNP 1-3 to be localized in azurophil granules. These studies define a broad-spectrum antimicrobial system in human neutrophils. The defensin system may operate in conjunction with or independently from oxygen-dependent microbicidal processes to enable human neutrophils to inactivate and destroy potential pathogens. |
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E ; SZKLAREK, D ; HARWIG, S. S. L ; DAHER, K ; BAINTON, D. F ; LEHRER, R. I</creator><creatorcontrib>GANZ, T ; SEISTED, M. E ; SZKLAREK, D ; HARWIG, S. S. L ; DAHER, K ; BAINTON, D. F ; LEHRER, R. I</creatorcontrib><description>We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-3, and which will be referred to as "defensins." HNP 1-3, a mixture of the three defensins, killed Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli effectively in vitro when tested in 10 mM phosphate buffer containing certain nutrients, but it had little or no bactericidal activity in nutrient-free buffer. In contrast, the nutrient-free buffer supported a high degree of activity by HNP 1-3 against Cryptococcus neoformans. In addition to its antibacterial and antifungal properties, HNP 1-3 directly inactivated herpes simplex virus, Type 1. Two of the individual purified defensins, HNP-1 and HNP-2, were as microbicidal as the mixture HNP 1-3. HNP-3 was less active than the other defensins against most but not all of the microbes tested. Immunoperoxidase stains revealed HNP 1-3 to have a granular localization in the neutrophil's cytoplasm by light microscopy. Frozen thin section immunogold transmission electron microscopy showed HNP 1-3 to be localized in azurophil granules. These studies define a broad-spectrum antimicrobial system in human neutrophils. The defensin system may operate in conjunction with or independently from oxygen-dependent microbicidal processes to enable human neutrophils to inactivate and destroy potential pathogens.</description><identifier>ISSN: 0021-9738</identifier><identifier>EISSN: 1558-8238</identifier><identifier>DOI: 10.1172/JCI112120</identifier><identifier>PMID: 2997278</identifier><identifier>CODEN: JCINAO</identifier><language>eng</language><publisher>Ann Arbor, MI: American Society for Clinical Investigation</publisher><subject>alpha-Defensins ; Amino Acids - analysis ; Bacteria - drug effects ; Bacteriology ; Biological and medical sciences ; Blood Proteins - isolation & purification ; Blood Proteins - pharmacology ; Blood Proteins - physiology ; Chromatography ; Cryptococcus neoformans - drug effects ; Cytoplasmic Granules - analysis ; Electrophoresis, Polyacrylamide Gel ; Fundamental and applied biological sciences. Psychology ; Humans ; Microbial Sensitivity Tests ; Microbiology ; Neutrophils - analysis ; Neutrophils - physiology ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Simplexvirus - drug effects</subject><ispartof>The Journal of clinical investigation, 1985-10, Vol.76 (4), p.1427-1435</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c509t-5e83340dd616df0b506b7ec634cec2b3352d718e0d5155e25ec5aed6c5ab86703</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/PMC424093/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC424093/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8492004$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2997278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>GANZ, T</creatorcontrib><creatorcontrib>SEISTED, M. E</creatorcontrib><creatorcontrib>SZKLAREK, D</creatorcontrib><creatorcontrib>HARWIG, S. S. L</creatorcontrib><creatorcontrib>DAHER, K</creatorcontrib><creatorcontrib>BAINTON, D. F</creatorcontrib><creatorcontrib>LEHRER, R. I</creatorcontrib><title>Defensins: natural peptide antibiotics of human neutrophils</title><title>The Journal of clinical investigation</title><addtitle>J Clin Invest</addtitle><description>We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-3, and which will be referred to as "defensins." HNP 1-3, a mixture of the three defensins, killed Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli effectively in vitro when tested in 10 mM phosphate buffer containing certain nutrients, but it had little or no bactericidal activity in nutrient-free buffer. In contrast, the nutrient-free buffer supported a high degree of activity by HNP 1-3 against Cryptococcus neoformans. In addition to its antibacterial and antifungal properties, HNP 1-3 directly inactivated herpes simplex virus, Type 1. Two of the individual purified defensins, HNP-1 and HNP-2, were as microbicidal as the mixture HNP 1-3. HNP-3 was less active than the other defensins against most but not all of the microbes tested. Immunoperoxidase stains revealed HNP 1-3 to have a granular localization in the neutrophil's cytoplasm by light microscopy. Frozen thin section immunogold transmission electron microscopy showed HNP 1-3 to be localized in azurophil granules. These studies define a broad-spectrum antimicrobial system in human neutrophils. The defensin system may operate in conjunction with or independently from oxygen-dependent microbicidal processes to enable human neutrophils to inactivate and destroy potential pathogens.</description><subject>alpha-Defensins</subject><subject>Amino Acids - analysis</subject><subject>Bacteria - drug effects</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Blood Proteins - isolation & purification</subject><subject>Blood Proteins - pharmacology</subject><subject>Blood Proteins - physiology</subject><subject>Chromatography</subject><subject>Cryptococcus neoformans - drug effects</subject><subject>Cytoplasmic Granules - analysis</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology</subject><subject>Neutrophils - analysis</subject><subject>Neutrophils - physiology</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Simplexvirus - drug effects</subject><issn>0021-9738</issn><issn>1558-8238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctKxDAUhoMo43hZ-ABCFyK4qObapIoLGW8jA250HdL01Im0aW1awbe3MqXoys05i_87hw9-hI4IPidE0ounxZIQSijeQnMihIoVZWobzTGmJE4lU7toL4R3jAnngs_QjKappFLN0dUtFOCD8-Ey8qbrW1NGDTSdyyEyvnOZqztnQ1QX0bqvjI889F1bN2tXhgO0U5gywOG499Hr_d3L4jFePT8sFzer2AqcdrEAxRjHeZ6QJC9wJnCSSbAJ4xYszRgTNJdEAc7F4A5UgBUG8mSYmUokZvvoevO36bMKcgu-GzR107rKtF-6Nk7_Tbxb67f6U3PKccqG-9Pxvq0_egidrlywUJbGQ90HLZMBTLn4FyRcJkwqPoBnG9C2dQgtFJMMwfqnET01MrDHv-0ncqxgyE_G3ARryqI13rowYYqnFGPOvgEnCJN4</recordid><startdate>19851001</startdate><enddate>19851001</enddate><creator>GANZ, T</creator><creator>SEISTED, M. E</creator><creator>SZKLAREK, D</creator><creator>HARWIG, S. S. L</creator><creator>DAHER, K</creator><creator>BAINTON, D. F</creator><creator>LEHRER, R. I</creator><general>American Society for Clinical Investigation</general><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>19851001</creationdate><title>Defensins: natural peptide antibiotics of human neutrophils</title><author>GANZ, T ; SEISTED, M. E ; SZKLAREK, D ; HARWIG, S. S. L ; DAHER, K ; BAINTON, D. F ; LEHRER, R. I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c509t-5e83340dd616df0b506b7ec634cec2b3352d718e0d5155e25ec5aed6c5ab86703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>alpha-Defensins</topic><topic>Amino Acids - analysis</topic><topic>Bacteria - drug effects</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Blood Proteins - isolation & purification</topic><topic>Blood Proteins - pharmacology</topic><topic>Blood Proteins - physiology</topic><topic>Chromatography</topic><topic>Cryptococcus neoformans - drug effects</topic><topic>Cytoplasmic Granules - analysis</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbiology</topic><topic>Neutrophils - analysis</topic><topic>Neutrophils - physiology</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Simplexvirus - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>GANZ, T</creatorcontrib><creatorcontrib>SEISTED, M. E</creatorcontrib><creatorcontrib>SZKLAREK, D</creatorcontrib><creatorcontrib>HARWIG, S. S. L</creatorcontrib><creatorcontrib>DAHER, K</creatorcontrib><creatorcontrib>BAINTON, D. F</creatorcontrib><creatorcontrib>LEHRER, R. 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I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defensins: natural peptide antibiotics of human neutrophils</atitle><jtitle>The Journal of clinical investigation</jtitle><addtitle>J Clin Invest</addtitle><date>1985-10-01</date><risdate>1985</risdate><volume>76</volume><issue>4</issue><spage>1427</spage><epage>1435</epage><pages>1427-1435</pages><issn>0021-9738</issn><eissn>1558-8238</eissn><coden>JCINAO</coden><abstract>We extracted a granule-rich sediment from normal human neutrophils and subjected it to chromatographic, electrophoretic, and functional analysis. The extract contained three small (molecular weight less than 3,500) antibiotic peptides that were named human neutrophil peptide (HNP)-1, HNP-2, and HNP-3, and which will be referred to as "defensins." HNP 1-3, a mixture of the three defensins, killed Staphylococcus aureus, Pseudomonas aeruginosa, and Escherichia coli effectively in vitro when tested in 10 mM phosphate buffer containing certain nutrients, but it had little or no bactericidal activity in nutrient-free buffer. In contrast, the nutrient-free buffer supported a high degree of activity by HNP 1-3 against Cryptococcus neoformans. In addition to its antibacterial and antifungal properties, HNP 1-3 directly inactivated herpes simplex virus, Type 1. Two of the individual purified defensins, HNP-1 and HNP-2, were as microbicidal as the mixture HNP 1-3. HNP-3 was less active than the other defensins against most but not all of the microbes tested. Immunoperoxidase stains revealed HNP 1-3 to have a granular localization in the neutrophil's cytoplasm by light microscopy. Frozen thin section immunogold transmission electron microscopy showed HNP 1-3 to be localized in azurophil granules. These studies define a broad-spectrum antimicrobial system in human neutrophils. The defensin system may operate in conjunction with or independently from oxygen-dependent microbicidal processes to enable human neutrophils to inactivate and destroy potential pathogens.</abstract><cop>Ann Arbor, MI</cop><pub>American Society for Clinical Investigation</pub><pmid>2997278</pmid><doi>10.1172/JCI112120</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alpha-Defensins Amino Acids - analysis Bacteria - drug effects Bacteriology Biological and medical sciences Blood Proteins - isolation & purification Blood Proteins - pharmacology Blood Proteins - physiology Chromatography Cryptococcus neoformans - drug effects Cytoplasmic Granules - analysis Electrophoresis, Polyacrylamide Gel Fundamental and applied biological sciences. Psychology Humans Microbial Sensitivity Tests Microbiology Neutrophils - analysis Neutrophils - physiology Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Simplexvirus - drug effects |
title | Defensins: natural peptide antibiotics of human neutrophils |
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