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
Hauptverfasser: Nishio, Mari, Urakawa, Naoki, Shigeoka, Manabu, Takase, Nobuhisa, Ichihara, Yumi, Arai, Noriaki, Koma, Yu-ichiro, Yokozaki, Hiroshi
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container_issue 2
container_start_page 83
container_title Pathology international
container_volume 66
creator Nishio, Mari
Urakawa, Naoki
Shigeoka, Manabu
Takase, Nobuhisa
Ichihara, Yumi
Arai, Noriaki
Koma, Yu-ichiro
Yokozaki, Hiroshi
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.
doi_str_mv 10.1111/pin.12381
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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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