Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages
Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major, whereas less information is available for L. (L) amazonensis. Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (...
Gespeichert in:
Veröffentlicht in: | PloS one 2010-11, Vol.5 (11), p.e13815 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 11 |
container_start_page | e13815 |
container_title | PloS one |
container_volume | 5 |
creator | de Souza Carmo, Erico Vinícius Katz, Simone Barbiéri, Clara Lúcia |
description | Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major, whereas less information is available for L. (L) amazonensis. Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (L.) amazonensis (C3H/HePas). In contrast, the susceptible strain (BALB/c) displayed a predominance of macrophages harboring a high number of amastigotes and very few neutrophils. These findings led us to investigate the interaction of inflammatory neutrophils with L. (L.) amazonensis-infected macrophages in vitro.
Mouse peritoneal macrophages infected with L. (L.) amazonensis were co-cultured with inflammatory neutrophils, and after four days, the infection was quantified microscopically. Data are representative of three experiments with similar results. The main findings were 1) intracellular parasites were efficiently destroyed in the co-cultures; 2) the leishmanicidal effect was similar when cells were obtained from mouse strains resistant (C3H/HePas) or susceptible (BALB/c) to L. (L.) amazonensis; 3) parasite destruction did not require contact between infected macrophages and neutrophils; 4) tumor necrosis factor alpha (TNF-α), neutrophil elastase and platelet activating factor (PAF) were involved with the leishmanicidal activity, and 5) destruction of the parasites did not depend on generation of oxygen or nitrogen radicals, indicating that parasite clearance did not involve the classical pathway of macrophage activation by TNF-α, as reported for other Leishmania species.
The present results provide evidence that neutrophils in concert with macrophages play a previously unrecognized leishmanicidal effect on L. (L.) amazonensis. We believe these findings may help to understand the mechanisms involved in innate immunity in cutaneous infection by this Leishmania species. |
doi_str_mv | 10.1371/journal.pone.0013815 |
format | Article |
fullrecord | <record><control><sourceid>gale_plos_</sourceid><recordid>TN_cdi_plos_journals_1295200750</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A473838787</galeid><doaj_id>oai_doaj_org_article_9ed96e62b5a74ff6b80abda74c9e05f2</doaj_id><sourcerecordid>A473838787</sourcerecordid><originalsourceid>FETCH-LOGICAL-c624t-43e85bbb8dcc98a16936486645ae6f2204cebecb13c553cc01e9c0f847a7f4e43</originalsourceid><addsrcrecordid>eNptUk1v1DAQjRCIlsI_QBCJA3DYxd8fF6Sq4qPSCi5wtmxnsutVEi92ggS_HodNSxdVPng0fu_NG89U1XOM1phK_G4fpzTYbn2IA6wRwlRh_qA6x5qSlSCIPrwTn1VPct4jxKkS4nF1RjBSJU3OK_cFpjHFwy50uU7QTB7qcQf1wSabwwi1m1IDQx2GegMh73o7BFu_-Re_rW1vfxcPQw55FYYW_AhN3Vs_q9ot5KfVo9Z2GZ4t90X1_eOHb1efV5uvn66vLjcrLwgbV4yC4s451XivlcVCU8GKXcYtiJYQxDw48A5Tzzn1HmHQHrWKSStbBoxeVC-PuocuZrN8TzaYaE4QkhwVxPUR0US7N4cUept-mWiD-ZuIaWtsGoPvwGhotABBHLeSta1wClnXlNhrQLwlRev9Um1yPTQehjHZ7kT09GUIO7ONPw3Rkkgpi8DrRSDFHxPk0fQhe-g6O0CcslGCaY40UgX56j_k_c0tqK0t_ssgYinrZ01zySRVVEk1V13fgyqngT74MsY2lPwJgR0JZZ45J2hvW8TIzIt4Y8bMi2iWRSy0F3e_55Z0s3n0DyGp3Ig</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1295200750</pqid></control><display><type>article</type><title>Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Public Library of Science (PLoS)</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>de Souza Carmo, Erico Vinícius ; Katz, Simone ; Barbiéri, Clara Lúcia</creator><contributor>Matloubian, Mehrdad</contributor><creatorcontrib>de Souza Carmo, Erico Vinícius ; Katz, Simone ; Barbiéri, Clara Lúcia ; Matloubian, Mehrdad</creatorcontrib><description>Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major, whereas less information is available for L. (L) amazonensis. Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (L.) amazonensis (C3H/HePas). In contrast, the susceptible strain (BALB/c) displayed a predominance of macrophages harboring a high number of amastigotes and very few neutrophils. These findings led us to investigate the interaction of inflammatory neutrophils with L. (L.) amazonensis-infected macrophages in vitro.
Mouse peritoneal macrophages infected with L. (L.) amazonensis were co-cultured with inflammatory neutrophils, and after four days, the infection was quantified microscopically. Data are representative of three experiments with similar results. The main findings were 1) intracellular parasites were efficiently destroyed in the co-cultures; 2) the leishmanicidal effect was similar when cells were obtained from mouse strains resistant (C3H/HePas) or susceptible (BALB/c) to L. (L.) amazonensis; 3) parasite destruction did not require contact between infected macrophages and neutrophils; 4) tumor necrosis factor alpha (TNF-α), neutrophil elastase and platelet activating factor (PAF) were involved with the leishmanicidal activity, and 5) destruction of the parasites did not depend on generation of oxygen or nitrogen radicals, indicating that parasite clearance did not involve the classical pathway of macrophage activation by TNF-α, as reported for other Leishmania species.
The present results provide evidence that neutrophils in concert with macrophages play a previously unrecognized leishmanicidal effect on L. (L.) amazonensis. We believe these findings may help to understand the mechanisms involved in innate immunity in cutaneous infection by this Leishmania species.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0013815</identifier><identifier>PMID: 21082032</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Amastigotes ; Amino Acid Chloromethyl Ketones - pharmacology ; Animals ; Antibodies - immunology ; Antibodies - pharmacology ; Azepines - pharmacology ; Cell activation ; Cell Communication - immunology ; Cells, Cultured ; Classical pathway ; Coculture Techniques ; Cytokines ; Cytokines - immunology ; Cytokines - metabolism ; Cytotoxicity ; Destruction ; Elastase ; Enzymes ; Female ; Free radicals ; Granulocytes ; Health aspects ; Host-Parasite Interactions - drug effects ; Immunity ; Immunology/Immunity to Infections ; Immunology/Innate Immunity ; In vitro methods and tests ; Infection ; Infections ; Infectious Diseases/Neglected Tropical Diseases ; Infectious Diseases/Protozoal Infections ; Inflammation ; Innate immunity ; Leishmania ; Leishmania - physiology ; Leishmania amazonensis ; Leishmania major ; Leukocyte Elastase - antagonists & inhibitors ; Leukocyte Elastase - metabolism ; Leukocytes (neutrophilic) ; Macrophages ; Macrophages, Peritoneal - immunology ; Macrophages, Peritoneal - metabolism ; Macrophages, Peritoneal - parasitology ; Metabolism ; Metabolites ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C3H ; Microscopy ; Microscopy, Fluorescence ; Neutrophils ; Neutrophils - cytology ; Neutrophils - immunology ; Neutrophils - metabolism ; Nitric Oxide - metabolism ; Nitrogen radicals ; Oxygen ; Parasites ; Peritoneum ; Platelet Activating Factor - antagonists & inhibitors ; Platelet Activating Factor - metabolism ; Platelet-activating factor ; Reactive Oxygen Species - metabolism ; Rodents ; Triazoles - pharmacology ; Tumor Necrosis Factor-alpha - immunology ; Tumor Necrosis Factor-alpha - metabolism ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α</subject><ispartof>PloS one, 2010-11, Vol.5 (11), p.e13815</ispartof><rights>COPYRIGHT 2010 Public Library of Science</rights><rights>2010 Carmo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Carmo et al. 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c624t-43e85bbb8dcc98a16936486645ae6f2204cebecb13c553cc01e9c0f847a7f4e43</citedby><cites>FETCH-LOGICAL-c624t-43e85bbb8dcc98a16936486645ae6f2204cebecb13c553cc01e9c0f847a7f4e43</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/PMC2972777/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972777/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21082032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Matloubian, Mehrdad</contributor><creatorcontrib>de Souza Carmo, Erico Vinícius</creatorcontrib><creatorcontrib>Katz, Simone</creatorcontrib><creatorcontrib>Barbiéri, Clara Lúcia</creatorcontrib><title>Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major, whereas less information is available for L. (L) amazonensis. Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (L.) amazonensis (C3H/HePas). In contrast, the susceptible strain (BALB/c) displayed a predominance of macrophages harboring a high number of amastigotes and very few neutrophils. These findings led us to investigate the interaction of inflammatory neutrophils with L. (L.) amazonensis-infected macrophages in vitro.
Mouse peritoneal macrophages infected with L. (L.) amazonensis were co-cultured with inflammatory neutrophils, and after four days, the infection was quantified microscopically. Data are representative of three experiments with similar results. The main findings were 1) intracellular parasites were efficiently destroyed in the co-cultures; 2) the leishmanicidal effect was similar when cells were obtained from mouse strains resistant (C3H/HePas) or susceptible (BALB/c) to L. (L.) amazonensis; 3) parasite destruction did not require contact between infected macrophages and neutrophils; 4) tumor necrosis factor alpha (TNF-α), neutrophil elastase and platelet activating factor (PAF) were involved with the leishmanicidal activity, and 5) destruction of the parasites did not depend on generation of oxygen or nitrogen radicals, indicating that parasite clearance did not involve the classical pathway of macrophage activation by TNF-α, as reported for other Leishmania species.
The present results provide evidence that neutrophils in concert with macrophages play a previously unrecognized leishmanicidal effect on L. (L.) amazonensis. We believe these findings may help to understand the mechanisms involved in innate immunity in cutaneous infection by this Leishmania species.</description><subject>Amastigotes</subject><subject>Amino Acid Chloromethyl Ketones - pharmacology</subject><subject>Animals</subject><subject>Antibodies - immunology</subject><subject>Antibodies - pharmacology</subject><subject>Azepines - pharmacology</subject><subject>Cell activation</subject><subject>Cell Communication - immunology</subject><subject>Cells, Cultured</subject><subject>Classical pathway</subject><subject>Coculture Techniques</subject><subject>Cytokines</subject><subject>Cytokines - immunology</subject><subject>Cytokines - metabolism</subject><subject>Cytotoxicity</subject><subject>Destruction</subject><subject>Elastase</subject><subject>Enzymes</subject><subject>Female</subject><subject>Free radicals</subject><subject>Granulocytes</subject><subject>Health aspects</subject><subject>Host-Parasite Interactions - drug effects</subject><subject>Immunity</subject><subject>Immunology/Immunity to Infections</subject><subject>Immunology/Innate Immunity</subject><subject>In vitro methods and tests</subject><subject>Infection</subject><subject>Infections</subject><subject>Infectious Diseases/Neglected Tropical Diseases</subject><subject>Infectious Diseases/Protozoal Infections</subject><subject>Inflammation</subject><subject>Innate immunity</subject><subject>Leishmania</subject><subject>Leishmania - physiology</subject><subject>Leishmania amazonensis</subject><subject>Leishmania major</subject><subject>Leukocyte Elastase - antagonists & inhibitors</subject><subject>Leukocyte Elastase - metabolism</subject><subject>Leukocytes (neutrophilic)</subject><subject>Macrophages</subject><subject>Macrophages, Peritoneal - immunology</subject><subject>Macrophages, Peritoneal - metabolism</subject><subject>Macrophages, Peritoneal - parasitology</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C3H</subject><subject>Microscopy</subject><subject>Microscopy, Fluorescence</subject><subject>Neutrophils</subject><subject>Neutrophils - cytology</subject><subject>Neutrophils - immunology</subject><subject>Neutrophils - metabolism</subject><subject>Nitric Oxide - metabolism</subject><subject>Nitrogen radicals</subject><subject>Oxygen</subject><subject>Parasites</subject><subject>Peritoneum</subject><subject>Platelet Activating Factor - antagonists & inhibitors</subject><subject>Platelet Activating Factor - metabolism</subject><subject>Platelet-activating factor</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Rodents</subject><subject>Triazoles - pharmacology</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsI_QBCJA3DYxd8fF6Sq4qPSCi5wtmxnsutVEi92ggS_HodNSxdVPng0fu_NG89U1XOM1phK_G4fpzTYbn2IA6wRwlRh_qA6x5qSlSCIPrwTn1VPct4jxKkS4nF1RjBSJU3OK_cFpjHFwy50uU7QTB7qcQf1wSabwwi1m1IDQx2GegMh73o7BFu_-Re_rW1vfxcPQw55FYYW_AhN3Vs_q9ot5KfVo9Z2GZ4t90X1_eOHb1efV5uvn66vLjcrLwgbV4yC4s451XivlcVCU8GKXcYtiJYQxDw48A5Tzzn1HmHQHrWKSStbBoxeVC-PuocuZrN8TzaYaE4QkhwVxPUR0US7N4cUept-mWiD-ZuIaWtsGoPvwGhotABBHLeSta1wClnXlNhrQLwlRev9Um1yPTQehjHZ7kT09GUIO7ONPw3Rkkgpi8DrRSDFHxPk0fQhe-g6O0CcslGCaY40UgX56j_k_c0tqK0t_ssgYinrZ01zySRVVEk1V13fgyqngT74MsY2lPwJgR0JZZ45J2hvW8TIzIt4Y8bMi2iWRSy0F3e_55Z0s3n0DyGp3Ig</recordid><startdate>20101103</startdate><enddate>20101103</enddate><creator>de Souza Carmo, Erico Vinícius</creator><creator>Katz, Simone</creator><creator>Barbiéri, Clara Lúcia</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20101103</creationdate><title>Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages</title><author>de Souza Carmo, Erico Vinícius ; Katz, Simone ; Barbiéri, Clara Lúcia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c624t-43e85bbb8dcc98a16936486645ae6f2204cebecb13c553cc01e9c0f847a7f4e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Amastigotes</topic><topic>Amino Acid Chloromethyl Ketones - pharmacology</topic><topic>Animals</topic><topic>Antibodies - immunology</topic><topic>Antibodies - pharmacology</topic><topic>Azepines - pharmacology</topic><topic>Cell activation</topic><topic>Cell Communication - immunology</topic><topic>Cells, Cultured</topic><topic>Classical pathway</topic><topic>Coculture Techniques</topic><topic>Cytokines</topic><topic>Cytokines - immunology</topic><topic>Cytokines - metabolism</topic><topic>Cytotoxicity</topic><topic>Destruction</topic><topic>Elastase</topic><topic>Enzymes</topic><topic>Female</topic><topic>Free radicals</topic><topic>Granulocytes</topic><topic>Health aspects</topic><topic>Host-Parasite Interactions - drug effects</topic><topic>Immunity</topic><topic>Immunology/Immunity to Infections</topic><topic>Immunology/Innate Immunity</topic><topic>In vitro methods and tests</topic><topic>Infection</topic><topic>Infections</topic><topic>Infectious Diseases/Neglected Tropical Diseases</topic><topic>Infectious Diseases/Protozoal Infections</topic><topic>Inflammation</topic><topic>Innate immunity</topic><topic>Leishmania</topic><topic>Leishmania - physiology</topic><topic>Leishmania amazonensis</topic><topic>Leishmania major</topic><topic>Leukocyte Elastase - antagonists & inhibitors</topic><topic>Leukocyte Elastase - metabolism</topic><topic>Leukocytes (neutrophilic)</topic><topic>Macrophages</topic><topic>Macrophages, Peritoneal - immunology</topic><topic>Macrophages, Peritoneal - metabolism</topic><topic>Macrophages, Peritoneal - parasitology</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C3H</topic><topic>Microscopy</topic><topic>Microscopy, Fluorescence</topic><topic>Neutrophils</topic><topic>Neutrophils - cytology</topic><topic>Neutrophils - immunology</topic><topic>Neutrophils - metabolism</topic><topic>Nitric Oxide - metabolism</topic><topic>Nitrogen radicals</topic><topic>Oxygen</topic><topic>Parasites</topic><topic>Peritoneum</topic><topic>Platelet Activating Factor - antagonists & inhibitors</topic><topic>Platelet Activating Factor - metabolism</topic><topic>Platelet-activating factor</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Rodents</topic><topic>Triazoles - pharmacology</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Souza Carmo, Erico Vinícius</creatorcontrib><creatorcontrib>Katz, Simone</creatorcontrib><creatorcontrib>Barbiéri, Clara Lúcia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Souza Carmo, Erico Vinícius</au><au>Katz, Simone</au><au>Barbiéri, Clara Lúcia</au><au>Matloubian, Mehrdad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2010-11-03</date><risdate>2010</risdate><volume>5</volume><issue>11</issue><spage>e13815</spage><pages>e13815-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Studies on the role of neutrophils in Leishmania infection were mainly performed with L. (L) major, whereas less information is available for L. (L) amazonensis. Previous results from our laboratory showed a large infiltrate of neutrophils in the site of infection in a mouse strain resistant to L. (L.) amazonensis (C3H/HePas). In contrast, the susceptible strain (BALB/c) displayed a predominance of macrophages harboring a high number of amastigotes and very few neutrophils. These findings led us to investigate the interaction of inflammatory neutrophils with L. (L.) amazonensis-infected macrophages in vitro.
Mouse peritoneal macrophages infected with L. (L.) amazonensis were co-cultured with inflammatory neutrophils, and after four days, the infection was quantified microscopically. Data are representative of three experiments with similar results. The main findings were 1) intracellular parasites were efficiently destroyed in the co-cultures; 2) the leishmanicidal effect was similar when cells were obtained from mouse strains resistant (C3H/HePas) or susceptible (BALB/c) to L. (L.) amazonensis; 3) parasite destruction did not require contact between infected macrophages and neutrophils; 4) tumor necrosis factor alpha (TNF-α), neutrophil elastase and platelet activating factor (PAF) were involved with the leishmanicidal activity, and 5) destruction of the parasites did not depend on generation of oxygen or nitrogen radicals, indicating that parasite clearance did not involve the classical pathway of macrophage activation by TNF-α, as reported for other Leishmania species.
The present results provide evidence that neutrophils in concert with macrophages play a previously unrecognized leishmanicidal effect on L. (L.) amazonensis. We believe these findings may help to understand the mechanisms involved in innate immunity in cutaneous infection by this Leishmania species.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21082032</pmid><doi>10.1371/journal.pone.0013815</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2010-11, Vol.5 (11), p.e13815 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1295200750 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Amastigotes Amino Acid Chloromethyl Ketones - pharmacology Animals Antibodies - immunology Antibodies - pharmacology Azepines - pharmacology Cell activation Cell Communication - immunology Cells, Cultured Classical pathway Coculture Techniques Cytokines Cytokines - immunology Cytokines - metabolism Cytotoxicity Destruction Elastase Enzymes Female Free radicals Granulocytes Health aspects Host-Parasite Interactions - drug effects Immunity Immunology/Immunity to Infections Immunology/Innate Immunity In vitro methods and tests Infection Infections Infectious Diseases/Neglected Tropical Diseases Infectious Diseases/Protozoal Infections Inflammation Innate immunity Leishmania Leishmania - physiology Leishmania amazonensis Leishmania major Leukocyte Elastase - antagonists & inhibitors Leukocyte Elastase - metabolism Leukocytes (neutrophilic) Macrophages Macrophages, Peritoneal - immunology Macrophages, Peritoneal - metabolism Macrophages, Peritoneal - parasitology Metabolism Metabolites Mice Mice, Inbred BALB C Mice, Inbred C3H Microscopy Microscopy, Fluorescence Neutrophils Neutrophils - cytology Neutrophils - immunology Neutrophils - metabolism Nitric Oxide - metabolism Nitrogen radicals Oxygen Parasites Peritoneum Platelet Activating Factor - antagonists & inhibitors Platelet Activating Factor - metabolism Platelet-activating factor Reactive Oxygen Species - metabolism Rodents Triazoles - pharmacology Tumor Necrosis Factor-alpha - immunology Tumor Necrosis Factor-alpha - metabolism Tumor necrosis factor-TNF Tumor necrosis factor-α |
title | Neutrophils reduce the parasite burden in Leishmania (Leishmania) amazonensis-infected macrophages |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T16%3A33%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Neutrophils%20reduce%20the%20parasite%20burden%20in%20Leishmania%20(Leishmania)%20amazonensis-infected%20macrophages&rft.jtitle=PloS%20one&rft.au=de%20Souza%20Carmo,%20Erico%20Vin%C3%ADcius&rft.date=2010-11-03&rft.volume=5&rft.issue=11&rft.spage=e13815&rft.pages=e13815-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0013815&rft_dat=%3Cgale_plos_%3EA473838787%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1295200750&rft_id=info:pmid/21082032&rft_galeid=A473838787&rft_doaj_id=oai_doaj_org_article_9ed96e62b5a74ff6b80abda74c9e05f2&rfr_iscdi=true |