Software-assisted morphometric and phenotype analyses of human peripheral blood monocyte-derived macrophages induced by a microenvironment model of human esophageal squamous cell carcinoma
Human macrophages play important roles in tumor promotion and are called tumor‐associated macrophages (TAMs). We previously demonstrated that human esophageal squamous cell carcinomas (ESCCs) contain TAMs and that these TAMs tend to have tumor‐supporting features. Here we exposed human macrophages t...
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Veröffentlicht in: | Pathology international 2016-02, Vol.66 (2), p.83-93 |
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description | Human macrophages play important roles in tumor promotion and are called tumor‐associated macrophages (TAMs). We previously demonstrated that human esophageal squamous cell carcinomas (ESCCs) contain TAMs and that these TAMs tend to have tumor‐supporting features. Here we exposed human macrophages to conditioned media of TE‐series human ESCC cell lines (TECMs) to generate an ESCC extracellular stimuli‐influenced TAM model. CD14+ peripheral blood monocytes (PBMos) from healthy donors were treated with M‐CSF and with additional IL‐4 or TECM exposure. Morphological changes of the cells and the induction of CD163/CD204 proteins were detected in the TECM‐exposed model TAMs by immunofluorescence. A software‐assisted immunofluorescent cell image analysis showed increased CD163/CD204 positivity in the model TAMs and a weak to moderate positive correlation between the cytoplasmic area and the sum fluorescent intensity of CD204. Morphological changes of the cells were significantly reflected by several cytomorphometric parameters. PBMos were elongated with M‐CSF treatment, then enlarged with TECM exposure. The cytoplasmic aspect ratio was decreased by M‐CSF treatment and slightly increased by TECM exposure. The nuclear‐cytoplasmic ratio decreased during the whole process of cell differentiation. This system is useful for quantitative assessments of TAM‐like morphological changes of macrophages and the induction of CD163/CD204 in a model ESCC microenvironment. |
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We previously demonstrated that human esophageal squamous cell carcinomas (ESCCs) contain TAMs and that these TAMs tend to have tumor‐supporting features. Here we exposed human macrophages to conditioned media of TE‐series human ESCC cell lines (TECMs) to generate an ESCC extracellular stimuli‐influenced TAM model. CD14+ peripheral blood monocytes (PBMos) from healthy donors were treated with M‐CSF and with additional IL‐4 or TECM exposure. Morphological changes of the cells and the induction of CD163/CD204 proteins were detected in the TECM‐exposed model TAMs by immunofluorescence. A software‐assisted immunofluorescent cell image analysis showed increased CD163/CD204 positivity in the model TAMs and a weak to moderate positive correlation between the cytoplasmic area and the sum fluorescent intensity of CD204. Morphological changes of the cells were significantly reflected by several cytomorphometric parameters. PBMos were elongated with M‐CSF treatment, then enlarged with TECM exposure. The cytoplasmic aspect ratio was decreased by M‐CSF treatment and slightly increased by TECM exposure. The nuclear‐cytoplasmic ratio decreased during the whole process of cell differentiation. This system is useful for quantitative assessments of TAM‐like morphological changes of macrophages and the induction of CD163/CD204 in a model ESCC microenvironment.</description><identifier>ISSN: 1320-5463</identifier><identifier>EISSN: 1440-1827</identifier><identifier>DOI: 10.1111/pin.12381</identifier><identifier>PMID: 26778807</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Antigens, CD - metabolism ; Antigens, Differentiation, Myelomonocytic - metabolism ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - pathology ; Cell Differentiation ; Cell Line, Tumor ; Culture Media, Conditioned ; esophageal cancer ; Esophageal Neoplasms - metabolism ; Esophageal Neoplasms - pathology ; Esophageal Squamous Cell Carcinoma ; Humans ; image analysis ; Image Processing, Computer-Assisted ; Interleukin-4 - pharmacology ; macrophages ; Macrophages - metabolism ; Macrophages - pathology ; Monocytes - metabolism ; Monocytes - pathology ; Phenotype ; Receptors, Cell Surface - metabolism ; Scavenger Receptors, Class A - metabolism ; Software ; Tumor Microenvironment</subject><ispartof>Pathology international, 2016-02, Vol.66 (2), p.83-93</ispartof><rights>2016 The Authors Pathology International published by Japanese Society of Pathology and John Wiley & Sons Australia, Ltd.</rights><rights>2016 Japanese Society of Pathology and John Wiley & Sons Australia, Ltd .</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4221-5280c6e07f02cb85be031f6e2117a506c53956bd6ea7ce1ba0190963270bdb993</citedby><cites>FETCH-LOGICAL-c4221-5280c6e07f02cb85be031f6e2117a506c53956bd6ea7ce1ba0190963270bdb993</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fpin.12381$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fpin.12381$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26778807$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nishio, Mari</creatorcontrib><creatorcontrib>Urakawa, Naoki</creatorcontrib><creatorcontrib>Shigeoka, Manabu</creatorcontrib><creatorcontrib>Takase, Nobuhisa</creatorcontrib><creatorcontrib>Ichihara, Yumi</creatorcontrib><creatorcontrib>Arai, Noriaki</creatorcontrib><creatorcontrib>Koma, Yu-ichiro</creatorcontrib><creatorcontrib>Yokozaki, Hiroshi</creatorcontrib><title>Software-assisted morphometric and phenotype analyses of human peripheral blood monocyte-derived macrophages induced by a microenvironment model of human esophageal squamous cell carcinoma</title><title>Pathology international</title><addtitle>Pathol Int</addtitle><description>Human macrophages play important roles in tumor promotion and are called tumor‐associated macrophages (TAMs). We previously demonstrated that human esophageal squamous cell carcinomas (ESCCs) contain TAMs and that these TAMs tend to have tumor‐supporting features. Here we exposed human macrophages to conditioned media of TE‐series human ESCC cell lines (TECMs) to generate an ESCC extracellular stimuli‐influenced TAM model. CD14+ peripheral blood monocytes (PBMos) from healthy donors were treated with M‐CSF and with additional IL‐4 or TECM exposure. Morphological changes of the cells and the induction of CD163/CD204 proteins were detected in the TECM‐exposed model TAMs by immunofluorescence. A software‐assisted immunofluorescent cell image analysis showed increased CD163/CD204 positivity in the model TAMs and a weak to moderate positive correlation between the cytoplasmic area and the sum fluorescent intensity of CD204. Morphological changes of the cells were significantly reflected by several cytomorphometric parameters. PBMos were elongated with M‐CSF treatment, then enlarged with TECM exposure. The cytoplasmic aspect ratio was decreased by M‐CSF treatment and slightly increased by TECM exposure. The nuclear‐cytoplasmic ratio decreased during the whole process of cell differentiation. This system is useful for quantitative assessments of TAM‐like morphological changes of macrophages and the induction of CD163/CD204 in a model ESCC microenvironment.</description><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, Myelomonocytic - metabolism</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Differentiation</subject><subject>Cell Line, Tumor</subject><subject>Culture Media, Conditioned</subject><subject>esophageal cancer</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Squamous Cell Carcinoma</subject><subject>Humans</subject><subject>image analysis</subject><subject>Image Processing, Computer-Assisted</subject><subject>Interleukin-4 - pharmacology</subject><subject>macrophages</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - pathology</subject><subject>Monocytes - metabolism</subject><subject>Monocytes - pathology</subject><subject>Phenotype</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Scavenger Receptors, Class A - metabolism</subject><subject>Software</subject><subject>Tumor Microenvironment</subject><issn>1320-5463</issn><issn>1440-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1u1TAQhSMEoj-w4AWQl3SR1j-JnSzRFbSVLgXUVl1ajjPhGmI7tZO2eTceDoe0ZYU39njO-TT2ybJ3BB-TtE4G444JZRV5ke2TosA5qah4mc6M4rwsONvLDmL8iTERjOPX2R7lQlQVFvvZ70vfjfcqQK5iNHGEFlkfhp23MAajkXItGnbg_DgPkCrVzxEi8h3aTVY5NEAwqR9Uj5re-8XtvJ5HyNvUuVtwSgc_7NSPZDOunXS6a2akkDWpAe7OBO8suDFZW-j_oSGutoSOt5OyfopIQ98jrYI2zlv1JnvVqT7C28f9MLv-_Olqc5Zvv56ebz5uc11QSvKSVlhzwKLDVDdV2QBmpONACRGqxFyXrC5503JQQgNpFCY1rjmjAjdtU9fsMPuwcofgbyeIo7QmLqMoB2kqSQQnOP0ow0l6tErT22IM0MkhGKvCLAmWS1gyhSX_hpW07x-xU2OhfVY-pZMEJ6vg3vQw_58kv51fPCHz1bFE-fDsUOGX5IKJUt5cnMrq-5fNll1dyoL9ASiwswA</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Nishio, Mari</creator><creator>Urakawa, Naoki</creator><creator>Shigeoka, Manabu</creator><creator>Takase, Nobuhisa</creator><creator>Ichihara, Yumi</creator><creator>Arai, Noriaki</creator><creator>Koma, Yu-ichiro</creator><creator>Yokozaki, Hiroshi</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>24P</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>7X8</scope></search><sort><creationdate>201602</creationdate><title>Software-assisted morphometric and phenotype analyses of human peripheral blood monocyte-derived macrophages induced by a microenvironment model of human esophageal squamous cell carcinoma</title><author>Nishio, Mari ; Urakawa, Naoki ; Shigeoka, Manabu ; Takase, Nobuhisa ; Ichihara, Yumi ; Arai, Noriaki ; Koma, Yu-ichiro ; Yokozaki, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4221-5280c6e07f02cb85be031f6e2117a506c53956bd6ea7ce1ba0190963270bdb993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, Myelomonocytic - metabolism</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Differentiation</topic><topic>Cell Line, Tumor</topic><topic>Culture Media, Conditioned</topic><topic>esophageal cancer</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Squamous Cell Carcinoma</topic><topic>Humans</topic><topic>image analysis</topic><topic>Image Processing, Computer-Assisted</topic><topic>Interleukin-4 - pharmacology</topic><topic>macrophages</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - pathology</topic><topic>Monocytes - metabolism</topic><topic>Monocytes - pathology</topic><topic>Phenotype</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Scavenger Receptors, Class A - metabolism</topic><topic>Software</topic><topic>Tumor Microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nishio, Mari</creatorcontrib><creatorcontrib>Urakawa, Naoki</creatorcontrib><creatorcontrib>Shigeoka, Manabu</creatorcontrib><creatorcontrib>Takase, Nobuhisa</creatorcontrib><creatorcontrib>Ichihara, Yumi</creatorcontrib><creatorcontrib>Arai, Noriaki</creatorcontrib><creatorcontrib>Koma, Yu-ichiro</creatorcontrib><creatorcontrib>Yokozaki, Hiroshi</creatorcontrib><collection>Istex</collection><collection>Wiley Online Library Open Access</collection><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><jtitle>Pathology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nishio, Mari</au><au>Urakawa, Naoki</au><au>Shigeoka, Manabu</au><au>Takase, Nobuhisa</au><au>Ichihara, Yumi</au><au>Arai, Noriaki</au><au>Koma, Yu-ichiro</au><au>Yokozaki, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Software-assisted morphometric and phenotype analyses of human peripheral blood monocyte-derived macrophages induced by a microenvironment model of human esophageal squamous cell carcinoma</atitle><jtitle>Pathology international</jtitle><addtitle>Pathol Int</addtitle><date>2016-02</date><risdate>2016</risdate><volume>66</volume><issue>2</issue><spage>83</spage><epage>93</epage><pages>83-93</pages><issn>1320-5463</issn><eissn>1440-1827</eissn><abstract>Human macrophages play important roles in tumor promotion and are called tumor‐associated macrophages (TAMs). We previously demonstrated that human esophageal squamous cell carcinomas (ESCCs) contain TAMs and that these TAMs tend to have tumor‐supporting features. Here we exposed human macrophages to conditioned media of TE‐series human ESCC cell lines (TECMs) to generate an ESCC extracellular stimuli‐influenced TAM model. CD14+ peripheral blood monocytes (PBMos) from healthy donors were treated with M‐CSF and with additional IL‐4 or TECM exposure. Morphological changes of the cells and the induction of CD163/CD204 proteins were detected in the TECM‐exposed model TAMs by immunofluorescence. A software‐assisted immunofluorescent cell image analysis showed increased CD163/CD204 positivity in the model TAMs and a weak to moderate positive correlation between the cytoplasmic area and the sum fluorescent intensity of CD204. Morphological changes of the cells were significantly reflected by several cytomorphometric parameters. PBMos were elongated with M‐CSF treatment, then enlarged with TECM exposure. The cytoplasmic aspect ratio was decreased by M‐CSF treatment and slightly increased by TECM exposure. The nuclear‐cytoplasmic ratio decreased during the whole process of cell differentiation. This system is useful for quantitative assessments of TAM‐like morphological changes of macrophages and the induction of CD163/CD204 in a model ESCC microenvironment.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>26778807</pmid><doi>10.1111/pin.12381</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - pathology Cell Differentiation Cell Line, Tumor Culture Media, Conditioned esophageal cancer Esophageal Neoplasms - metabolism Esophageal Neoplasms - pathology Esophageal Squamous Cell Carcinoma Humans image analysis Image Processing, Computer-Assisted Interleukin-4 - pharmacology macrophages Macrophages - metabolism Macrophages - pathology Monocytes - metabolism Monocytes - pathology Phenotype Receptors, Cell Surface - metabolism Scavenger Receptors, Class A - metabolism Software Tumor Microenvironment |
title | Software-assisted morphometric and phenotype analyses of human peripheral blood monocyte-derived macrophages induced by a microenvironment model of human esophageal squamous cell carcinoma |
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