Loading…

Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment

Exposure to an enriched environment (EE) affects not only brain functions but also immune responses upon viral or bacterial infections. In this study, we examined changes in the phagocytic response and chemokine production of resident peritoneal macrophages after mice had been housed under EE condit...

Full description

Saved in:
Bibliographic Details
Published in:International immunopharmacology 2018-12, Vol.65, p.44-49
Main Authors: Otaki, Momoko, Hirano, Tetsuya, Yamaguchi, Yohko, Kaida, Kohei, Koshika, Seiji, Nagata, Kisaburo, Nishimura, Mayumi, Kakinuma, Shizuko, Shimada, Yoshiya, Kobayashi, Yoshiro
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173
cites cdi_FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173
container_end_page 49
container_issue
container_start_page 44
container_title International immunopharmacology
container_volume 65
creator Otaki, Momoko
Hirano, Tetsuya
Yamaguchi, Yohko
Kaida, Kohei
Koshika, Seiji
Nagata, Kisaburo
Nishimura, Mayumi
Kakinuma, Shizuko
Shimada, Yoshiya
Kobayashi, Yoshiro
description Exposure to an enriched environment (EE) affects not only brain functions but also immune responses upon viral or bacterial infections. In this study, we examined changes in the phagocytic response and chemokine production of resident peritoneal macrophages after mice had been housed under EE conditions for 6 or 8 weeks, and then explored the possibility that EE could cause a change in the macrophage phenotype by means of flow cytometry as well as quantitative RT-PCR. The percentages of EE macrophages phagocytosing S. aureus and apoptotic neutrophils were significantly larger than those of standard environment (SE) macrophages. After coculturing with S. aureus, EE macrophages tended to produce greater amounts of chemokines such as MIP-2, KC and MCP-1 than SE ones, although the increases for MIP-2 and KC were not statistically significant. As compared with SE macrophages, EE macrophages included more CD40-positive cells (M1 marker), and expressed more mRNAs of IL-6 (M1 marker) and IRF4 (M2 marker), and less mRNA of CD38 (M1 marker), suggesting either the possibility that EE macrophages are a mixed population of M1 and M2 macrophages or the possibility that they are a unique population with a mixed M1 and M2 macrophage phenotype. •An enriched environment (EE) increased phagocytosis of S. aureus by macrophages.•EE increased phagocytosis of apoptotic neutrophils by macrophages.•EE tended to increase S. aureus-induced chemokine production by macrophages.•EE macrophages showed a mixed M1 and M2 macrophage phenotype.
doi_str_mv 10.1016/j.intimp.2018.09.037
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2115754203</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1567576918307380</els_id><sourcerecordid>2115754203</sourcerecordid><originalsourceid>FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173</originalsourceid><addsrcrecordid>eNp9kU2L1TAUhosozof-A5GAGzetSZvPjSAXHYUBN7oOaXI6zeU26STpwPz7SbmjCxeucgjP-56Pt2neEdwRTPinY-dD8cva9ZjIDqsOD-JFc0mkkC0RmL2sNeOiZYKri-Yq5yPG9Z-S183FgHsxKMIvm_vDbMIdZOQDKjOgaQu2-BiQCQ6tM4RYHldAcUIJsncQCloh-RIDmBNajE1xnc1uYKYCCc1xyz7c7XYmIAjJ2xlcLR58imGp-jfNq8mcMrx9fq-b39--_jp8b29_3vw4fLltLcO4tGZgFI9KEAXCgGVu5KORklGuXC9ZP9KJSgABfKTMKWmk4Axc7xRYKogYrpuPZ981xfsNctGLzxZOJxOgDql7QphgtMdDRT_8gx7jlkKdrlKcY8UHsVP0TNWdc04w6TX5xaRHTbDeI9FHfY5E75ForHSNpMreP5tv4wLur-hPBhX4fAagXuPBQ9LZeggWnE9gi3bR_7_DE0fvoEQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2166096373</pqid></control><display><type>article</type><title>Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment</title><source>ScienceDirect Freedom Collection</source><creator>Otaki, Momoko ; Hirano, Tetsuya ; Yamaguchi, Yohko ; Kaida, Kohei ; Koshika, Seiji ; Nagata, Kisaburo ; Nishimura, Mayumi ; Kakinuma, Shizuko ; Shimada, Yoshiya ; Kobayashi, Yoshiro</creator><creatorcontrib>Otaki, Momoko ; Hirano, Tetsuya ; Yamaguchi, Yohko ; Kaida, Kohei ; Koshika, Seiji ; Nagata, Kisaburo ; Nishimura, Mayumi ; Kakinuma, Shizuko ; Shimada, Yoshiya ; Kobayashi, Yoshiro</creatorcontrib><description>Exposure to an enriched environment (EE) affects not only brain functions but also immune responses upon viral or bacterial infections. In this study, we examined changes in the phagocytic response and chemokine production of resident peritoneal macrophages after mice had been housed under EE conditions for 6 or 8 weeks, and then explored the possibility that EE could cause a change in the macrophage phenotype by means of flow cytometry as well as quantitative RT-PCR. The percentages of EE macrophages phagocytosing S. aureus and apoptotic neutrophils were significantly larger than those of standard environment (SE) macrophages. After coculturing with S. aureus, EE macrophages tended to produce greater amounts of chemokines such as MIP-2, KC and MCP-1 than SE ones, although the increases for MIP-2 and KC were not statistically significant. As compared with SE macrophages, EE macrophages included more CD40-positive cells (M1 marker), and expressed more mRNAs of IL-6 (M1 marker) and IRF4 (M2 marker), and less mRNA of CD38 (M1 marker), suggesting either the possibility that EE macrophages are a mixed population of M1 and M2 macrophages or the possibility that they are a unique population with a mixed M1 and M2 macrophage phenotype. •An enriched environment (EE) increased phagocytosis of S. aureus by macrophages.•EE increased phagocytosis of apoptotic neutrophils by macrophages.•EE tended to increase S. aureus-induced chemokine production by macrophages.•EE macrophages showed a mixed M1 and M2 macrophage phenotype.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2018.09.037</identifier><identifier>PMID: 30273916</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Apoptosis ; Bacterial infections ; Biomarkers ; Brain ; CD38 antigen ; CD40 antigen ; Chemokines ; Chemokines - genetics ; Chemokines - metabolism ; Coculture Techniques ; Enriched environment ; Enrichment ; Flow cytometry ; Gene Expression Regulation ; Genotype &amp; phenotype ; Housing ; Housing, Animal ; Immune response ; Interferon regulatory factor 4 ; Interleukin 6 ; Leukocytes (neutrophilic) ; Macrophage inflammatory protein ; Macrophages ; Macrophages, Peritoneal - classification ; Macrophages, Peritoneal - physiology ; Male ; Mice ; Mice, Inbred C57BL ; Monocyte chemoattractant protein 1 ; mRNA ; Neutrophils ; Peritoneum ; Phagocytes ; Phagocytosis ; Phenotype ; Phenotypes ; Polymerase chain reaction ; Resident peritoneal macrophages ; Staphylococcus aureus ; Statistical analysis</subject><ispartof>International immunopharmacology, 2018-12, Vol.65, p.44-49</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Dec 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173</citedby><cites>FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30273916$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Otaki, Momoko</creatorcontrib><creatorcontrib>Hirano, Tetsuya</creatorcontrib><creatorcontrib>Yamaguchi, Yohko</creatorcontrib><creatorcontrib>Kaida, Kohei</creatorcontrib><creatorcontrib>Koshika, Seiji</creatorcontrib><creatorcontrib>Nagata, Kisaburo</creatorcontrib><creatorcontrib>Nishimura, Mayumi</creatorcontrib><creatorcontrib>Kakinuma, Shizuko</creatorcontrib><creatorcontrib>Shimada, Yoshiya</creatorcontrib><creatorcontrib>Kobayashi, Yoshiro</creatorcontrib><title>Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Exposure to an enriched environment (EE) affects not only brain functions but also immune responses upon viral or bacterial infections. In this study, we examined changes in the phagocytic response and chemokine production of resident peritoneal macrophages after mice had been housed under EE conditions for 6 or 8 weeks, and then explored the possibility that EE could cause a change in the macrophage phenotype by means of flow cytometry as well as quantitative RT-PCR. The percentages of EE macrophages phagocytosing S. aureus and apoptotic neutrophils were significantly larger than those of standard environment (SE) macrophages. After coculturing with S. aureus, EE macrophages tended to produce greater amounts of chemokines such as MIP-2, KC and MCP-1 than SE ones, although the increases for MIP-2 and KC were not statistically significant. As compared with SE macrophages, EE macrophages included more CD40-positive cells (M1 marker), and expressed more mRNAs of IL-6 (M1 marker) and IRF4 (M2 marker), and less mRNA of CD38 (M1 marker), suggesting either the possibility that EE macrophages are a mixed population of M1 and M2 macrophages or the possibility that they are a unique population with a mixed M1 and M2 macrophage phenotype. •An enriched environment (EE) increased phagocytosis of S. aureus by macrophages.•EE increased phagocytosis of apoptotic neutrophils by macrophages.•EE tended to increase S. aureus-induced chemokine production by macrophages.•EE macrophages showed a mixed M1 and M2 macrophage phenotype.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Bacterial infections</subject><subject>Biomarkers</subject><subject>Brain</subject><subject>CD38 antigen</subject><subject>CD40 antigen</subject><subject>Chemokines</subject><subject>Chemokines - genetics</subject><subject>Chemokines - metabolism</subject><subject>Coculture Techniques</subject><subject>Enriched environment</subject><subject>Enrichment</subject><subject>Flow cytometry</subject><subject>Gene Expression Regulation</subject><subject>Genotype &amp; phenotype</subject><subject>Housing</subject><subject>Housing, Animal</subject><subject>Immune response</subject><subject>Interferon regulatory factor 4</subject><subject>Interleukin 6</subject><subject>Leukocytes (neutrophilic)</subject><subject>Macrophage inflammatory protein</subject><subject>Macrophages</subject><subject>Macrophages, Peritoneal - classification</subject><subject>Macrophages, Peritoneal - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Monocyte chemoattractant protein 1</subject><subject>mRNA</subject><subject>Neutrophils</subject><subject>Peritoneum</subject><subject>Phagocytes</subject><subject>Phagocytosis</subject><subject>Phenotype</subject><subject>Phenotypes</subject><subject>Polymerase chain reaction</subject><subject>Resident peritoneal macrophages</subject><subject>Staphylococcus aureus</subject><subject>Statistical analysis</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kU2L1TAUhosozof-A5GAGzetSZvPjSAXHYUBN7oOaXI6zeU26STpwPz7SbmjCxeucgjP-56Pt2neEdwRTPinY-dD8cva9ZjIDqsOD-JFc0mkkC0RmL2sNeOiZYKri-Yq5yPG9Z-S183FgHsxKMIvm_vDbMIdZOQDKjOgaQu2-BiQCQ6tM4RYHldAcUIJsncQCloh-RIDmBNajE1xnc1uYKYCCc1xyz7c7XYmIAjJ2xlcLR58imGp-jfNq8mcMrx9fq-b39--_jp8b29_3vw4fLltLcO4tGZgFI9KEAXCgGVu5KORklGuXC9ZP9KJSgABfKTMKWmk4Axc7xRYKogYrpuPZ981xfsNctGLzxZOJxOgDql7QphgtMdDRT_8gx7jlkKdrlKcY8UHsVP0TNWdc04w6TX5xaRHTbDeI9FHfY5E75ForHSNpMreP5tv4wLur-hPBhX4fAagXuPBQ9LZeggWnE9gi3bR_7_DE0fvoEQ</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Otaki, Momoko</creator><creator>Hirano, Tetsuya</creator><creator>Yamaguchi, Yohko</creator><creator>Kaida, Kohei</creator><creator>Koshika, Seiji</creator><creator>Nagata, Kisaburo</creator><creator>Nishimura, Mayumi</creator><creator>Kakinuma, Shizuko</creator><creator>Shimada, Yoshiya</creator><creator>Kobayashi, Yoshiro</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7QO</scope><scope>7T5</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20181201</creationdate><title>Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment</title><author>Otaki, Momoko ; Hirano, Tetsuya ; Yamaguchi, Yohko ; Kaida, Kohei ; Koshika, Seiji ; Nagata, Kisaburo ; Nishimura, Mayumi ; Kakinuma, Shizuko ; Shimada, Yoshiya ; Kobayashi, Yoshiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Bacterial infections</topic><topic>Biomarkers</topic><topic>Brain</topic><topic>CD38 antigen</topic><topic>CD40 antigen</topic><topic>Chemokines</topic><topic>Chemokines - genetics</topic><topic>Chemokines - metabolism</topic><topic>Coculture Techniques</topic><topic>Enriched environment</topic><topic>Enrichment</topic><topic>Flow cytometry</topic><topic>Gene Expression Regulation</topic><topic>Genotype &amp; phenotype</topic><topic>Housing</topic><topic>Housing, Animal</topic><topic>Immune response</topic><topic>Interferon regulatory factor 4</topic><topic>Interleukin 6</topic><topic>Leukocytes (neutrophilic)</topic><topic>Macrophage inflammatory protein</topic><topic>Macrophages</topic><topic>Macrophages, Peritoneal - classification</topic><topic>Macrophages, Peritoneal - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Monocyte chemoattractant protein 1</topic><topic>mRNA</topic><topic>Neutrophils</topic><topic>Peritoneum</topic><topic>Phagocytes</topic><topic>Phagocytosis</topic><topic>Phenotype</topic><topic>Phenotypes</topic><topic>Polymerase chain reaction</topic><topic>Resident peritoneal macrophages</topic><topic>Staphylococcus aureus</topic><topic>Statistical analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Otaki, Momoko</creatorcontrib><creatorcontrib>Hirano, Tetsuya</creatorcontrib><creatorcontrib>Yamaguchi, Yohko</creatorcontrib><creatorcontrib>Kaida, Kohei</creatorcontrib><creatorcontrib>Koshika, Seiji</creatorcontrib><creatorcontrib>Nagata, Kisaburo</creatorcontrib><creatorcontrib>Nishimura, Mayumi</creatorcontrib><creatorcontrib>Kakinuma, Shizuko</creatorcontrib><creatorcontrib>Shimada, Yoshiya</creatorcontrib><creatorcontrib>Kobayashi, Yoshiro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Otaki, Momoko</au><au>Hirano, Tetsuya</au><au>Yamaguchi, Yohko</au><au>Kaida, Kohei</au><au>Koshika, Seiji</au><au>Nagata, Kisaburo</au><au>Nishimura, Mayumi</au><au>Kakinuma, Shizuko</au><au>Shimada, Yoshiya</au><au>Kobayashi, Yoshiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>65</volume><spage>44</spage><epage>49</epage><pages>44-49</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>Exposure to an enriched environment (EE) affects not only brain functions but also immune responses upon viral or bacterial infections. In this study, we examined changes in the phagocytic response and chemokine production of resident peritoneal macrophages after mice had been housed under EE conditions for 6 or 8 weeks, and then explored the possibility that EE could cause a change in the macrophage phenotype by means of flow cytometry as well as quantitative RT-PCR. The percentages of EE macrophages phagocytosing S. aureus and apoptotic neutrophils were significantly larger than those of standard environment (SE) macrophages. After coculturing with S. aureus, EE macrophages tended to produce greater amounts of chemokines such as MIP-2, KC and MCP-1 than SE ones, although the increases for MIP-2 and KC were not statistically significant. As compared with SE macrophages, EE macrophages included more CD40-positive cells (M1 marker), and expressed more mRNAs of IL-6 (M1 marker) and IRF4 (M2 marker), and less mRNA of CD38 (M1 marker), suggesting either the possibility that EE macrophages are a mixed population of M1 and M2 macrophages or the possibility that they are a unique population with a mixed M1 and M2 macrophage phenotype. •An enriched environment (EE) increased phagocytosis of S. aureus by macrophages.•EE increased phagocytosis of apoptotic neutrophils by macrophages.•EE tended to increase S. aureus-induced chemokine production by macrophages.•EE macrophages showed a mixed M1 and M2 macrophage phenotype.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30273916</pmid><doi>10.1016/j.intimp.2018.09.037</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1567-5769
ispartof International immunopharmacology, 2018-12, Vol.65, p.44-49
issn 1567-5769
1878-1705
language eng
recordid cdi_proquest_miscellaneous_2115754203
source ScienceDirect Freedom Collection
subjects Animals
Apoptosis
Bacterial infections
Biomarkers
Brain
CD38 antigen
CD40 antigen
Chemokines
Chemokines - genetics
Chemokines - metabolism
Coculture Techniques
Enriched environment
Enrichment
Flow cytometry
Gene Expression Regulation
Genotype & phenotype
Housing
Housing, Animal
Immune response
Interferon regulatory factor 4
Interleukin 6
Leukocytes (neutrophilic)
Macrophage inflammatory protein
Macrophages
Macrophages, Peritoneal - classification
Macrophages, Peritoneal - physiology
Male
Mice
Mice, Inbred C57BL
Monocyte chemoattractant protein 1
mRNA
Neutrophils
Peritoneum
Phagocytes
Phagocytosis
Phenotype
Phenotypes
Polymerase chain reaction
Resident peritoneal macrophages
Staphylococcus aureus
Statistical analysis
title Changes in the function and phenotype of resident peritoneal macrophages after housing in an enriched environment
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T09%3A42%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Changes%20in%20the%20function%20and%20phenotype%20of%20resident%20peritoneal%20macrophages%20after%20housing%20in%20an%20enriched%20environment&rft.jtitle=International%20immunopharmacology&rft.au=Otaki,%20Momoko&rft.date=2018-12-01&rft.volume=65&rft.spage=44&rft.epage=49&rft.pages=44-49&rft.issn=1567-5769&rft.eissn=1878-1705&rft_id=info:doi/10.1016/j.intimp.2018.09.037&rft_dat=%3Cproquest_cross%3E2115754203%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c500t-a3540b9719e7aec5db6ba885469d2852b4f48ee7e6b45d98a8765ed2d9ec47173%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2166096373&rft_id=info:pmid/30273916&rfr_iscdi=true