The Influence of Low Oxygen on Macrophage Response to Leishmania Infection
Hypoxia (low oxygen tension) is a common feature of inflamed and infected tissues. The influence of hypoxia on macrophage responses to micro‐organisms has only recently been studied. This study demonstrates that hypoxia induced macrophages to control Leishmania amazonensis, an intracellular parasite...
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creator | Degrossoli, A. Arrais‐Silva, W. W. Colhone, M. C. Gadelha, F. R. Joazeiro, P. P. Giorgio, S. |
description | Hypoxia (low oxygen tension) is a common feature of inflamed and infected tissues. The influence of hypoxia on macrophage responses to micro‐organisms has only recently been studied. This study demonstrates that hypoxia induced macrophages to control Leishmania amazonensis, an intracellular parasite that causes cutaneous and cutaneous metastatic lesions. The mechanisms that contribute to the control of macrophages against L. amazonensis infection under a hypoxic microenvironment are not known. Nitric oxide, TNF‐α, IL‐10 or IL‐12 is not responsible for the decrease in parasitism under hypoxia. Live L. amazonensis entry or exocytosis of internalized particles as well as energetic metabolism was not impaired in infected macrophages; no apoptosis‐like death was detected in intracellular parasites. Reactive oxygen species (ROS) is likely to be involved, because treatment with antioxidants N‐acetylcysteine (NAC) and ebselen inhibits the leishmanicidal effect of macrophages under hypoxia. Leishmania amazonensis infection induces macrophages to express hypoxia‐inducible factor‐1 (HIF‐1α) and ‐2 (HIF‐2α). Data indicate that hypoxia affects the microbial activities and protein expression of macrophages leading to a different phenotype from that of the normoxic counterpart and that it plays a role in modulating Leishmania infection. |
doi_str_mv | 10.1111/j.1365-3083.2011.02566.x |
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W. ; Colhone, M. C. ; Gadelha, F. R. ; Joazeiro, P. P. ; Giorgio, S.</creator><creatorcontrib>Degrossoli, A. ; Arrais‐Silva, W. W. ; Colhone, M. C. ; Gadelha, F. R. ; Joazeiro, P. P. ; Giorgio, S.</creatorcontrib><description>Hypoxia (low oxygen tension) is a common feature of inflamed and infected tissues. The influence of hypoxia on macrophage responses to micro‐organisms has only recently been studied. This study demonstrates that hypoxia induced macrophages to control Leishmania amazonensis, an intracellular parasite that causes cutaneous and cutaneous metastatic lesions. The mechanisms that contribute to the control of macrophages against L. amazonensis infection under a hypoxic microenvironment are not known. Nitric oxide, TNF‐α, IL‐10 or IL‐12 is not responsible for the decrease in parasitism under hypoxia. Live L. amazonensis entry or exocytosis of internalized particles as well as energetic metabolism was not impaired in infected macrophages; no apoptosis‐like death was detected in intracellular parasites. Reactive oxygen species (ROS) is likely to be involved, because treatment with antioxidants N‐acetylcysteine (NAC) and ebselen inhibits the leishmanicidal effect of macrophages under hypoxia. Leishmania amazonensis infection induces macrophages to express hypoxia‐inducible factor‐1 (HIF‐1α) and ‐2 (HIF‐2α). Data indicate that hypoxia affects the microbial activities and protein expression of macrophages leading to a different phenotype from that of the normoxic counterpart and that it plays a role in modulating Leishmania infection.</description><identifier>ISSN: 0300-9475</identifier><identifier>EISSN: 1365-3083</identifier><identifier>DOI: 10.1111/j.1365-3083.2011.02566.x</identifier><identifier>PMID: 21517930</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Acetylcysteine ; Acetylcysteine - pharmacology ; Animals ; Antioxidants ; Azoles - pharmacology ; Basic Helix-Loop-Helix Transcription Factors - biosynthesis ; Basic Helix-Loop-Helix Transcription Factors - immunology ; Data processing ; Exocytosis ; Female ; Free Radical Scavengers - pharmacology ; Hypoxia ; Hypoxia - immunology ; Hypoxia - metabolism ; Hypoxia-inducible factor 1 ; Hypoxia-inducible factor 1 alpha ; Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis ; Hypoxia-Inducible Factor 1, alpha Subunit - immunology ; Infection ; Inflammation ; Interleukin 10 ; Interleukin 12 ; Interleukin-10 - immunology ; Interleukin-12 - immunology ; Leishmania amazonensis ; Leishmaniasis, Cutaneous - immunology ; Leishmaniasis, Cutaneous - metabolism ; Macrophages ; Macrophages - drug effects ; Macrophages - immunology ; Macrophages - metabolism ; Macrophages - ultrastructure ; Metabolism ; Metastases ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, Knockout ; Microenvironments ; Nitric oxide ; Nitric Oxide - immunology ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - immunology ; Organoselenium Compounds - pharmacology ; Oxygen tension ; Parasitism ; Reactive oxygen species ; Reactive Oxygen Species - immunology ; Reactive Oxygen Species - metabolism ; Tumor necrosis factor- alpha ; Tumor Necrosis Factor-alpha - immunology</subject><ispartof>Scandinavian journal of immunology, 2011-08, Vol.74 (2), p.165-175</ispartof><rights>2011 The Authors. Scandinavian Journal of Immunology © 2011 Blackwell Publishing Ltd</rights><rights>2011 The Authors. 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W.</creatorcontrib><creatorcontrib>Colhone, M. C.</creatorcontrib><creatorcontrib>Gadelha, F. R.</creatorcontrib><creatorcontrib>Joazeiro, P. P.</creatorcontrib><creatorcontrib>Giorgio, S.</creatorcontrib><title>The Influence of Low Oxygen on Macrophage Response to Leishmania Infection</title><title>Scandinavian journal of immunology</title><addtitle>Scand J Immunol</addtitle><description>Hypoxia (low oxygen tension) is a common feature of inflamed and infected tissues. The influence of hypoxia on macrophage responses to micro‐organisms has only recently been studied. This study demonstrates that hypoxia induced macrophages to control Leishmania amazonensis, an intracellular parasite that causes cutaneous and cutaneous metastatic lesions. The mechanisms that contribute to the control of macrophages against L. amazonensis infection under a hypoxic microenvironment are not known. Nitric oxide, TNF‐α, IL‐10 or IL‐12 is not responsible for the decrease in parasitism under hypoxia. Live L. amazonensis entry or exocytosis of internalized particles as well as energetic metabolism was not impaired in infected macrophages; no apoptosis‐like death was detected in intracellular parasites. Reactive oxygen species (ROS) is likely to be involved, because treatment with antioxidants N‐acetylcysteine (NAC) and ebselen inhibits the leishmanicidal effect of macrophages under hypoxia. Leishmania amazonensis infection induces macrophages to express hypoxia‐inducible factor‐1 (HIF‐1α) and ‐2 (HIF‐2α). Data indicate that hypoxia affects the microbial activities and protein expression of macrophages leading to a different phenotype from that of the normoxic counterpart and that it plays a role in modulating Leishmania infection.</description><subject>Acetylcysteine</subject><subject>Acetylcysteine - pharmacology</subject><subject>Animals</subject><subject>Antioxidants</subject><subject>Azoles - pharmacology</subject><subject>Basic Helix-Loop-Helix Transcription Factors - biosynthesis</subject><subject>Basic Helix-Loop-Helix Transcription Factors - immunology</subject><subject>Data processing</subject><subject>Exocytosis</subject><subject>Female</subject><subject>Free Radical Scavengers - pharmacology</subject><subject>Hypoxia</subject><subject>Hypoxia - immunology</subject><subject>Hypoxia - metabolism</subject><subject>Hypoxia-inducible factor 1</subject><subject>Hypoxia-inducible factor 1 alpha</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis</subject><subject>Hypoxia-Inducible Factor 1, alpha Subunit - immunology</subject><subject>Infection</subject><subject>Inflammation</subject><subject>Interleukin 10</subject><subject>Interleukin 12</subject><subject>Interleukin-10 - immunology</subject><subject>Interleukin-12 - immunology</subject><subject>Leishmania amazonensis</subject><subject>Leishmaniasis, Cutaneous - immunology</subject><subject>Leishmaniasis, Cutaneous - metabolism</subject><subject>Macrophages</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - ultrastructure</subject><subject>Metabolism</subject><subject>Metastases</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Microenvironments</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - immunology</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - immunology</subject><subject>Organoselenium Compounds - pharmacology</subject><subject>Oxygen tension</subject><subject>Parasitism</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - immunology</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Tumor necrosis factor- alpha</subject><subject>Tumor Necrosis Factor-alpha - immunology</subject><issn>0300-9475</issn><issn>1365-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOwzAQRS0EgvL4BeQdq4SZ2EnsBQuEeBQVVeKxtlxnQlOlcYlb0f49CYVuwZuxNOeOPYcxjhBjdy5nMYosjQQoESeAGEOSZlm83mODXWOfDUAARFrm6RE7DmEGgCLJxSE7SjDFXAsYsMfXKfFhU9YrahxxX_KR_-Tj9eadGu4b_mRd6xdT-078mcLCN4H40vMRVWE6t01l-zC5ZeWbU3ZQ2jrQ2U89YW93t683D9FofD-8uR5FTqaQRRNlncYyyTNZpNJ2v8idloJA6QIzVaBGnYArJoAlEAp0CTpKJKpuNUASJ-xiO3fR-o8VhaWZV8FRXduG_CoYpRRCKmX2N5mnUoOSuiPVluy2DaGl0izaam7bjUEwvXIzM71Z05s1vXLzrdysu-j5zyOryZyKXfDXcQdcbYHPqqbNvwebl8dhfxNfKCaNAw</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Degrossoli, A.</creator><creator>Arrais‐Silva, W. W.</creator><creator>Colhone, M. C.</creator><creator>Gadelha, F. R.</creator><creator>Joazeiro, P. P.</creator><creator>Giorgio, S.</creator><general>Blackwell Publishing Ltd</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>7X8</scope><scope>7T5</scope><scope>H94</scope><scope>M7N</scope></search><sort><creationdate>201108</creationdate><title>The Influence of Low Oxygen on Macrophage Response to Leishmania Infection</title><author>Degrossoli, A. ; Arrais‐Silva, W. W. ; Colhone, M. C. ; Gadelha, F. R. ; Joazeiro, P. P. ; Giorgio, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4506-b8ac91f2764d54a9307c943e089d168d191920cdb01f0e131c21ce241813601e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Acetylcysteine</topic><topic>Acetylcysteine - pharmacology</topic><topic>Animals</topic><topic>Antioxidants</topic><topic>Azoles - pharmacology</topic><topic>Basic Helix-Loop-Helix Transcription Factors - biosynthesis</topic><topic>Basic Helix-Loop-Helix Transcription Factors - immunology</topic><topic>Data processing</topic><topic>Exocytosis</topic><topic>Female</topic><topic>Free Radical Scavengers - pharmacology</topic><topic>Hypoxia</topic><topic>Hypoxia - immunology</topic><topic>Hypoxia - metabolism</topic><topic>Hypoxia-inducible factor 1</topic><topic>Hypoxia-inducible factor 1 alpha</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis</topic><topic>Hypoxia-Inducible Factor 1, alpha Subunit - immunology</topic><topic>Infection</topic><topic>Inflammation</topic><topic>Interleukin 10</topic><topic>Interleukin 12</topic><topic>Interleukin-10 - immunology</topic><topic>Interleukin-12 - immunology</topic><topic>Leishmania amazonensis</topic><topic>Leishmaniasis, Cutaneous - immunology</topic><topic>Leishmaniasis, Cutaneous - metabolism</topic><topic>Macrophages</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - ultrastructure</topic><topic>Metabolism</topic><topic>Metastases</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Microenvironments</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - immunology</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Nitric Oxide Synthase Type II - immunology</topic><topic>Organoselenium Compounds - pharmacology</topic><topic>Oxygen tension</topic><topic>Parasitism</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - immunology</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Tumor necrosis factor- alpha</topic><topic>Tumor Necrosis Factor-alpha - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Degrossoli, A.</creatorcontrib><creatorcontrib>Arrais‐Silva, W. W.</creatorcontrib><creatorcontrib>Colhone, M. C.</creatorcontrib><creatorcontrib>Gadelha, F. R.</creatorcontrib><creatorcontrib>Joazeiro, P. P.</creatorcontrib><creatorcontrib>Giorgio, S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Scandinavian journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Degrossoli, A.</au><au>Arrais‐Silva, W. W.</au><au>Colhone, M. C.</au><au>Gadelha, F. R.</au><au>Joazeiro, P. P.</au><au>Giorgio, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Influence of Low Oxygen on Macrophage Response to Leishmania Infection</atitle><jtitle>Scandinavian journal of immunology</jtitle><addtitle>Scand J Immunol</addtitle><date>2011-08</date><risdate>2011</risdate><volume>74</volume><issue>2</issue><spage>165</spage><epage>175</epage><pages>165-175</pages><issn>0300-9475</issn><eissn>1365-3083</eissn><abstract>Hypoxia (low oxygen tension) is a common feature of inflamed and infected tissues. The influence of hypoxia on macrophage responses to micro‐organisms has only recently been studied. This study demonstrates that hypoxia induced macrophages to control Leishmania amazonensis, an intracellular parasite that causes cutaneous and cutaneous metastatic lesions. The mechanisms that contribute to the control of macrophages against L. amazonensis infection under a hypoxic microenvironment are not known. Nitric oxide, TNF‐α, IL‐10 or IL‐12 is not responsible for the decrease in parasitism under hypoxia. Live L. amazonensis entry or exocytosis of internalized particles as well as energetic metabolism was not impaired in infected macrophages; no apoptosis‐like death was detected in intracellular parasites. Reactive oxygen species (ROS) is likely to be involved, because treatment with antioxidants N‐acetylcysteine (NAC) and ebselen inhibits the leishmanicidal effect of macrophages under hypoxia. Leishmania amazonensis infection induces macrophages to express hypoxia‐inducible factor‐1 (HIF‐1α) and ‐2 (HIF‐2α). Data indicate that hypoxia affects the microbial activities and protein expression of macrophages leading to a different phenotype from that of the normoxic counterpart and that it plays a role in modulating Leishmania infection.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21517930</pmid><doi>10.1111/j.1365-3083.2011.02566.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetylcysteine Acetylcysteine - pharmacology Animals Antioxidants Azoles - pharmacology Basic Helix-Loop-Helix Transcription Factors - biosynthesis Basic Helix-Loop-Helix Transcription Factors - immunology Data processing Exocytosis Female Free Radical Scavengers - pharmacology Hypoxia Hypoxia - immunology Hypoxia - metabolism Hypoxia-inducible factor 1 Hypoxia-inducible factor 1 alpha Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis Hypoxia-Inducible Factor 1, alpha Subunit - immunology Infection Inflammation Interleukin 10 Interleukin 12 Interleukin-10 - immunology Interleukin-12 - immunology Leishmania amazonensis Leishmaniasis, Cutaneous - immunology Leishmaniasis, Cutaneous - metabolism Macrophages Macrophages - drug effects Macrophages - immunology Macrophages - metabolism Macrophages - ultrastructure Metabolism Metastases Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Knockout Microenvironments Nitric oxide Nitric Oxide - immunology Nitric Oxide Synthase Type II - genetics Nitric Oxide Synthase Type II - immunology Organoselenium Compounds - pharmacology Oxygen tension Parasitism Reactive oxygen species Reactive Oxygen Species - immunology Reactive Oxygen Species - metabolism Tumor necrosis factor- alpha Tumor Necrosis Factor-alpha - immunology |
title | The Influence of Low Oxygen on Macrophage Response to Leishmania Infection |
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