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...
Saved in:
Published in: | International immunopharmacology 2018-12, Vol.65, p.44-49 |
---|---|
Main Authors: | , , , , , , , , , |
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 & 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 & 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 & 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 |