Macrophages of Human First Trimester Decidua Express Markers Associated to Alternative Activation

Problem:  Depending on the type of their activation, macrophages may promote TH1‐ or TH2‐type of immune responses. To date, not much is known about the activation phenotype of decidua macrophages, which – together with NK cells – constitute the majority of bone marrow derived cells at this location....

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Veröffentlicht in:American journal of reproductive immunology (1989) 2004-02, Vol.51 (2), p.117-122
Hauptverfasser: Cupurdija, Kristijan, Azzola, Dagmar, Hainz, Ursula, Gratchev, Alexei, Heitger, Andreas, Takikawa, Osamu, Goerdt, Sergij, Wintersteiger, Reinhold, Dohr, Gottfried, Sedlmayr, Peter
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container_end_page 122
container_issue 2
container_start_page 117
container_title American journal of reproductive immunology (1989)
container_volume 51
creator Cupurdija, Kristijan
Azzola, Dagmar
Hainz, Ursula
Gratchev, Alexei
Heitger, Andreas
Takikawa, Osamu
Goerdt, Sergij
Wintersteiger, Reinhold
Dohr, Gottfried
Sedlmayr, Peter
description Problem:  Depending on the type of their activation, macrophages may promote TH1‐ or TH2‐type of immune responses. To date, not much is known about the activation phenotype of decidua macrophages, which – together with NK cells – constitute the majority of bone marrow derived cells at this location. Method of study:  The study was based on analysis of healthy first trimester decidua by immunohistochemistry and flow cytometry. We analyzed expression of markers characteristic for alternatively activated macrophages (Mφ2). Results:  The markers MS‐1 (stabilin‐1) and coagulation factor XIIIa were found expressed in the interior of decidua macrophages (DMφ). In contrast, indoleamine 2,3‐dioxygenase (IDO), an enzyme induced in macrophages by IFNγ, was not present in DMφ. Conclusions:  First trimester DMφ display phenotypic markers associated to alternatively activated macrophages. In addition, absence of IDO indicates that DMφ are not under a predominant influence of IFNγ.
doi_str_mv 10.1046/j.8755-8920.2003.00128.x
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To date, not much is known about the activation phenotype of decidua macrophages, which – together with NK cells – constitute the majority of bone marrow derived cells at this location. Method of study:  The study was based on analysis of healthy first trimester decidua by immunohistochemistry and flow cytometry. We analyzed expression of markers characteristic for alternatively activated macrophages (Mφ2). Results:  The markers MS‐1 (stabilin‐1) and coagulation factor XIIIa were found expressed in the interior of decidua macrophages (DMφ). In contrast, indoleamine 2,3‐dioxygenase (IDO), an enzyme induced in macrophages by IFNγ, was not present in DMφ. Conclusions:  First trimester DMφ display phenotypic markers associated to alternatively activated macrophages. 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To date, not much is known about the activation phenotype of decidua macrophages, which – together with NK cells – constitute the majority of bone marrow derived cells at this location. Method of study:  The study was based on analysis of healthy first trimester decidua by immunohistochemistry and flow cytometry. We analyzed expression of markers characteristic for alternatively activated macrophages (Mφ2). Results:  The markers MS‐1 (stabilin‐1) and coagulation factor XIIIa were found expressed in the interior of decidua macrophages (DMφ). In contrast, indoleamine 2,3‐dioxygenase (IDO), an enzyme induced in macrophages by IFNγ, was not present in DMφ. Conclusions:  First trimester DMφ display phenotypic markers associated to alternatively activated macrophages. 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Azzola, Dagmar ; Hainz, Ursula ; Gratchev, Alexei ; Heitger, Andreas ; Takikawa, Osamu ; Goerdt, Sergij ; Wintersteiger, Reinhold ; Dohr, Gottfried ; Sedlmayr, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5018-2e66eef967e4901ecb9eb5fe62a62611413bc6e49e056de21cc064da7e241cc53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Biomarkers</topic><topic>Cell Adhesion Molecules, Neuronal - biosynthesis</topic><topic>Cell Adhesion Molecules, Neuronal - immunology</topic><topic>Cell Culture Techniques</topic><topic>Decidua - immunology</topic><topic>Decidua - physiology</topic><topic>Dioxygenases</topic><topic>Factor VIIIa - biosynthesis</topic><topic>Factor VIIIa - immunology</topic><topic>Factor XIIIa</topic><topic>Female</topic><topic>Flow Cytometry</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunophenotyping</topic><topic>Indoleamine-Pyrrole 2,3,-Dioxygenase</topic><topic>Interferon-gamma - pharmacology</topic><topic>laser scanning microscopy</topic><topic>Macrophage Activation - drug effects</topic><topic>Macrophage Activation - immunology</topic><topic>Macrophage Activation - physiology</topic><topic>Macrophage Colony-Stimulating Factor - pharmacology</topic><topic>Macrophages - immunology</topic><topic>Macrophages - physiology</topic><topic>Mφ2</topic><topic>Oxygenases - biosynthesis</topic><topic>Oxygenases - immunology</topic><topic>placenta</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First - immunology</topic><topic>Pregnancy Trimester, First - physiology</topic><topic>Receptors, Lymphocyte Homing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cupurdija, Kristijan</creatorcontrib><creatorcontrib>Azzola, Dagmar</creatorcontrib><creatorcontrib>Hainz, Ursula</creatorcontrib><creatorcontrib>Gratchev, Alexei</creatorcontrib><creatorcontrib>Heitger, Andreas</creatorcontrib><creatorcontrib>Takikawa, Osamu</creatorcontrib><creatorcontrib>Goerdt, Sergij</creatorcontrib><creatorcontrib>Wintersteiger, Reinhold</creatorcontrib><creatorcontrib>Dohr, Gottfried</creatorcontrib><creatorcontrib>Sedlmayr, Peter</creatorcontrib><collection>Istex</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>MEDLINE - Academic</collection><jtitle>American journal of reproductive immunology (1989)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cupurdija, Kristijan</au><au>Azzola, Dagmar</au><au>Hainz, Ursula</au><au>Gratchev, Alexei</au><au>Heitger, Andreas</au><au>Takikawa, Osamu</au><au>Goerdt, Sergij</au><au>Wintersteiger, Reinhold</au><au>Dohr, Gottfried</au><au>Sedlmayr, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrophages of Human First Trimester Decidua Express Markers Associated to Alternative Activation</atitle><jtitle>American journal of reproductive immunology (1989)</jtitle><addtitle>Am J Reprod Immunol</addtitle><date>2004-02</date><risdate>2004</risdate><volume>51</volume><issue>2</issue><spage>117</spage><epage>122</epage><pages>117-122</pages><issn>1046-7408</issn><eissn>1600-0897</eissn><abstract>Problem:  Depending on the type of their activation, macrophages may promote TH1‐ or TH2‐type of immune responses. To date, not much is known about the activation phenotype of decidua macrophages, which – together with NK cells – constitute the majority of bone marrow derived cells at this location. Method of study:  The study was based on analysis of healthy first trimester decidua by immunohistochemistry and flow cytometry. We analyzed expression of markers characteristic for alternatively activated macrophages (Mφ2). Results:  The markers MS‐1 (stabilin‐1) and coagulation factor XIIIa were found expressed in the interior of decidua macrophages (DMφ). In contrast, indoleamine 2,3‐dioxygenase (IDO), an enzyme induced in macrophages by IFNγ, was not present in DMφ. Conclusions:  First trimester DMφ display phenotypic markers associated to alternatively activated macrophages. In addition, absence of IDO indicates that DMφ are not under a predominant influence of IFNγ.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing</pub><pmid>14748837</pmid><doi>10.1046/j.8755-8920.2003.00128.x</doi><tpages>6</tpages></addata></record>
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subjects Biomarkers
Cell Adhesion Molecules, Neuronal - biosynthesis
Cell Adhesion Molecules, Neuronal - immunology
Cell Culture Techniques
Decidua - immunology
Decidua - physiology
Dioxygenases
Factor VIIIa - biosynthesis
Factor VIIIa - immunology
Factor XIIIa
Female
Flow Cytometry
Humans
Immunohistochemistry
Immunophenotyping
Indoleamine-Pyrrole 2,3,-Dioxygenase
Interferon-gamma - pharmacology
laser scanning microscopy
Macrophage Activation - drug effects
Macrophage Activation - immunology
Macrophage Activation - physiology
Macrophage Colony-Stimulating Factor - pharmacology
Macrophages - immunology
Macrophages - physiology
Mφ2
Oxygenases - biosynthesis
Oxygenases - immunology
placenta
Pregnancy
Pregnancy Trimester, First - immunology
Pregnancy Trimester, First - physiology
Receptors, Lymphocyte Homing
title Macrophages of Human First Trimester Decidua Express Markers Associated to Alternative Activation
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