In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus
Many helminth parasites have evolved strategies to evade the immune response of their hosts, which includes immunomodulation. Prostaglandin E2 (PGE2) is one of the best-described immunomodulators in mammalian helminth parasite infections. We hypothesized that also in teleost fish anti-helminthic imm...
Gespeichert in:
Veröffentlicht in: | Fish & shellfish immunology 2014-12, Vol.41 (2), p.473-481 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 481 |
---|---|
container_issue | 2 |
container_start_page | 473 |
container_title | Fish & shellfish immunology |
container_volume | 41 |
creator | Kutyrev, Ivan A. Franke, Frederik Büscher, Janine Kurtz, Joachim Scharsack, Jörn P. |
description | Many helminth parasites have evolved strategies to evade the immune response of their hosts, which includes immunomodulation. Prostaglandin E2 (PGE2) is one of the best-described immunomodulators in mammalian helminth parasite infections. We hypothesized that also in teleost fish anti-helminthic immune responses are regulated via PGE2. We used a model system consisting of the tapeworm Schistocephalus solidus and its host, the three-spined stickleback (Gasterosteus aculeatus), to investigate in vitro effects of PGE2 on head kidney leucocytes (HKL) derived from sticklebacks that were experimentally infected with S. solidus. PGE2 was tested alone or in combination with either S. solidus antigens or bacterial lipopolysaccharides (LPS). After in vitro culture, cell viability and changes in leucocyte subpopulations (granulocytes to lymphocytes ratios) were monitored by flow cytometry and HKL were tested for their capacity to produce reactive oxygen species (ROS) with a chemiluminescence assay. In short term (2 h) HKL cultures PGE2 did not change the total numbers of live HKL, but the production of ROS decreased significantly with high (0.1 μmol L−1) PGE2 concentrations. In long-term (96 h) cultures high PGE2 concentrations induced a sharp decrease of leucocytes viability, while low (0.1 pmol L−1) and intermediate (0.1 nmol L−1) concentrations of PGE2 caused elevated leucocyte viability compared to controls. This coincided with reduced ROS production in cultures with high PGE2 and elevated ROS production in cultures with low PGE2. Granulocyte to lymphocyte ratios increased with high PGE2 concentrations alone and in combination with S. solidus antigens and LPS, most prominently with HKL from S. solidus infected sticklebacks. The present study supports the hypothesis that PGE2 might be an immunomodulator in tapeworm–fish parasite–host interactions.
[Display omitted]
•The highest concentration of PGE2 induced a sharp decrease of leucocytes viability.•Low concentrations of PGE2 caused increased leucocyte viability.•The highest concentration of PGE2 increased granulocyte to leucocyte ratios.•The highest concentration of PGE2 decreased reactive oxygen species activity.•PGE2 might be an immunomodulator in Cestode–fish parasite–host interactions. |
doi_str_mv | 10.1016/j.fsi.2014.09.031 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1647008455</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1050464814003660</els_id><sourcerecordid>1647008455</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2319-b8076915e467d4a16b69b53d1cf32daee05aec17e5c9eb3840577d448dea56543</originalsourceid><addsrcrecordid>eNqNkcFu1DAQhiMEoqXwAFyQj-WQME5sJxYnVLWlUiUOwNly7AnrbTZeMk6rvg19FZ4MR1vghjh5ZH3zyf7_onjNoeLA1bttNVCoauCiAl1Bw58Uxxy0LLUW7dN1llAKJbqj4gXRFgBUo-B5cVTLBnjL9XHxcDX9_HEb0hwZDgO6RCwObD9HSvbbaCcfJnZeszixERcX3X1CYsMcd4xScDcj9tbdEDu9tJRw3cKFmHXLiDYt9JaFaZWiZ1nFppj-XtyFtGFpg8whpeiRfXabkCeH-40ds4XiGPxCL4tngx0JXz2eJ8XXi_MvZx_L60-XV2cfrktXN1yXfQet0lyiUK0Xlqte6V42nruhqb1FBGnR8Ral09g3nQDZZlB0Hq1UUjQnxenBmz__fclvMrtADsccAsaFDFeiBeiElP-B1lpL1dZtRvkBdTkcmnEw-zns7HxvOJi1RLM1uUSzlmhAm1xi3nnzqF_6Hfo_G79by8D7A4A5j9uAsyEXcHLow5zDNT6Gf-h_AR1WsKk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1629956727</pqid></control><display><type>article</type><title>In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Kutyrev, Ivan A. ; Franke, Frederik ; Büscher, Janine ; Kurtz, Joachim ; Scharsack, Jörn P.</creator><creatorcontrib>Kutyrev, Ivan A. ; Franke, Frederik ; Büscher, Janine ; Kurtz, Joachim ; Scharsack, Jörn P.</creatorcontrib><description>Many helminth parasites have evolved strategies to evade the immune response of their hosts, which includes immunomodulation. Prostaglandin E2 (PGE2) is one of the best-described immunomodulators in mammalian helminth parasite infections. We hypothesized that also in teleost fish anti-helminthic immune responses are regulated via PGE2. We used a model system consisting of the tapeworm Schistocephalus solidus and its host, the three-spined stickleback (Gasterosteus aculeatus), to investigate in vitro effects of PGE2 on head kidney leucocytes (HKL) derived from sticklebacks that were experimentally infected with S. solidus. PGE2 was tested alone or in combination with either S. solidus antigens or bacterial lipopolysaccharides (LPS). After in vitro culture, cell viability and changes in leucocyte subpopulations (granulocytes to lymphocytes ratios) were monitored by flow cytometry and HKL were tested for their capacity to produce reactive oxygen species (ROS) with a chemiluminescence assay. In short term (2 h) HKL cultures PGE2 did not change the total numbers of live HKL, but the production of ROS decreased significantly with high (0.1 μmol L−1) PGE2 concentrations. In long-term (96 h) cultures high PGE2 concentrations induced a sharp decrease of leucocytes viability, while low (0.1 pmol L−1) and intermediate (0.1 nmol L−1) concentrations of PGE2 caused elevated leucocyte viability compared to controls. This coincided with reduced ROS production in cultures with high PGE2 and elevated ROS production in cultures with low PGE2. Granulocyte to lymphocyte ratios increased with high PGE2 concentrations alone and in combination with S. solidus antigens and LPS, most prominently with HKL from S. solidus infected sticklebacks. The present study supports the hypothesis that PGE2 might be an immunomodulator in tapeworm–fish parasite–host interactions.
[Display omitted]
•The highest concentration of PGE2 induced a sharp decrease of leucocytes viability.•Low concentrations of PGE2 caused increased leucocyte viability.•The highest concentration of PGE2 increased granulocyte to leucocyte ratios.•The highest concentration of PGE2 decreased reactive oxygen species activity.•PGE2 might be an immunomodulator in Cestode–fish parasite–host interactions.</description><identifier>ISSN: 1050-4648</identifier><identifier>EISSN: 1095-9947</identifier><identifier>DOI: 10.1016/j.fsi.2014.09.031</identifier><identifier>PMID: 25301719</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Analysis of Variance ; Animals ; Cell Survival - drug effects ; Cestoda ; Cestoda - immunology ; Dinoprostone - immunology ; Dinoprostone - pharmacology ; Flow Cytometry ; Gasterosteus aculeatus ; Head Kidney - cytology ; In Vitro Techniques ; In vitro leucocyte responses ; Leukocytes - drug effects ; Leukocytes - immunology ; Lipopolysaccharides ; Parasite immunomodulation ; Prostaglandin E2 ; Reactive Oxygen Species - metabolism ; Schistocephalus solidus ; Smegmamorpha - immunology ; Smegmamorpha - parasitology ; Teleostei</subject><ispartof>Fish & shellfish immunology, 2014-12, Vol.41 (2), p.473-481</ispartof><rights>2014 Elsevier Ltd</rights><rights>Copyright © 2014 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2319-b8076915e467d4a16b69b53d1cf32daee05aec17e5c9eb3840577d448dea56543</citedby><cites>FETCH-LOGICAL-c2319-b8076915e467d4a16b69b53d1cf32daee05aec17e5c9eb3840577d448dea56543</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1050464814003660$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25301719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kutyrev, Ivan A.</creatorcontrib><creatorcontrib>Franke, Frederik</creatorcontrib><creatorcontrib>Büscher, Janine</creatorcontrib><creatorcontrib>Kurtz, Joachim</creatorcontrib><creatorcontrib>Scharsack, Jörn P.</creatorcontrib><title>In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus</title><title>Fish & shellfish immunology</title><addtitle>Fish Shellfish Immunol</addtitle><description>Many helminth parasites have evolved strategies to evade the immune response of their hosts, which includes immunomodulation. Prostaglandin E2 (PGE2) is one of the best-described immunomodulators in mammalian helminth parasite infections. We hypothesized that also in teleost fish anti-helminthic immune responses are regulated via PGE2. We used a model system consisting of the tapeworm Schistocephalus solidus and its host, the three-spined stickleback (Gasterosteus aculeatus), to investigate in vitro effects of PGE2 on head kidney leucocytes (HKL) derived from sticklebacks that were experimentally infected with S. solidus. PGE2 was tested alone or in combination with either S. solidus antigens or bacterial lipopolysaccharides (LPS). After in vitro culture, cell viability and changes in leucocyte subpopulations (granulocytes to lymphocytes ratios) were monitored by flow cytometry and HKL were tested for their capacity to produce reactive oxygen species (ROS) with a chemiluminescence assay. In short term (2 h) HKL cultures PGE2 did not change the total numbers of live HKL, but the production of ROS decreased significantly with high (0.1 μmol L−1) PGE2 concentrations. In long-term (96 h) cultures high PGE2 concentrations induced a sharp decrease of leucocytes viability, while low (0.1 pmol L−1) and intermediate (0.1 nmol L−1) concentrations of PGE2 caused elevated leucocyte viability compared to controls. This coincided with reduced ROS production in cultures with high PGE2 and elevated ROS production in cultures with low PGE2. Granulocyte to lymphocyte ratios increased with high PGE2 concentrations alone and in combination with S. solidus antigens and LPS, most prominently with HKL from S. solidus infected sticklebacks. The present study supports the hypothesis that PGE2 might be an immunomodulator in tapeworm–fish parasite–host interactions.
[Display omitted]
•The highest concentration of PGE2 induced a sharp decrease of leucocytes viability.•Low concentrations of PGE2 caused increased leucocyte viability.•The highest concentration of PGE2 increased granulocyte to leucocyte ratios.•The highest concentration of PGE2 decreased reactive oxygen species activity.•PGE2 might be an immunomodulator in Cestode–fish parasite–host interactions.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Cell Survival - drug effects</subject><subject>Cestoda</subject><subject>Cestoda - immunology</subject><subject>Dinoprostone - immunology</subject><subject>Dinoprostone - pharmacology</subject><subject>Flow Cytometry</subject><subject>Gasterosteus aculeatus</subject><subject>Head Kidney - cytology</subject><subject>In Vitro Techniques</subject><subject>In vitro leucocyte responses</subject><subject>Leukocytes - drug effects</subject><subject>Leukocytes - immunology</subject><subject>Lipopolysaccharides</subject><subject>Parasite immunomodulation</subject><subject>Prostaglandin E2</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Schistocephalus solidus</subject><subject>Smegmamorpha - immunology</subject><subject>Smegmamorpha - parasitology</subject><subject>Teleostei</subject><issn>1050-4648</issn><issn>1095-9947</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkcFu1DAQhiMEoqXwAFyQj-WQME5sJxYnVLWlUiUOwNly7AnrbTZeMk6rvg19FZ4MR1vghjh5ZH3zyf7_onjNoeLA1bttNVCoauCiAl1Bw58Uxxy0LLUW7dN1llAKJbqj4gXRFgBUo-B5cVTLBnjL9XHxcDX9_HEb0hwZDgO6RCwObD9HSvbbaCcfJnZeszixERcX3X1CYsMcd4xScDcj9tbdEDu9tJRw3cKFmHXLiDYt9JaFaZWiZ1nFppj-XtyFtGFpg8whpeiRfXabkCeH-40ds4XiGPxCL4tngx0JXz2eJ8XXi_MvZx_L60-XV2cfrktXN1yXfQet0lyiUK0Xlqte6V42nruhqb1FBGnR8Ral09g3nQDZZlB0Hq1UUjQnxenBmz__fclvMrtADsccAsaFDFeiBeiElP-B1lpL1dZtRvkBdTkcmnEw-zns7HxvOJi1RLM1uUSzlmhAm1xi3nnzqF_6Hfo_G79by8D7A4A5j9uAsyEXcHLow5zDNT6Gf-h_AR1WsKk</recordid><startdate>201412</startdate><enddate>201412</enddate><creator>Kutyrev, Ivan A.</creator><creator>Franke, Frederik</creator><creator>Büscher, Janine</creator><creator>Kurtz, Joachim</creator><creator>Scharsack, Jörn P.</creator><general>Elsevier Ltd</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>7X8</scope><scope>7T5</scope><scope>F1W</scope><scope>H94</scope><scope>H95</scope><scope>H98</scope><scope>L.G</scope></search><sort><creationdate>201412</creationdate><title>In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus</title><author>Kutyrev, Ivan A. ; Franke, Frederik ; Büscher, Janine ; Kurtz, Joachim ; Scharsack, Jörn P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2319-b8076915e467d4a16b69b53d1cf32daee05aec17e5c9eb3840577d448dea56543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Cell Survival - drug effects</topic><topic>Cestoda</topic><topic>Cestoda - immunology</topic><topic>Dinoprostone - immunology</topic><topic>Dinoprostone - pharmacology</topic><topic>Flow Cytometry</topic><topic>Gasterosteus aculeatus</topic><topic>Head Kidney - cytology</topic><topic>In Vitro Techniques</topic><topic>In vitro leucocyte responses</topic><topic>Leukocytes - drug effects</topic><topic>Leukocytes - immunology</topic><topic>Lipopolysaccharides</topic><topic>Parasite immunomodulation</topic><topic>Prostaglandin E2</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Schistocephalus solidus</topic><topic>Smegmamorpha - immunology</topic><topic>Smegmamorpha - parasitology</topic><topic>Teleostei</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kutyrev, Ivan A.</creatorcontrib><creatorcontrib>Franke, Frederik</creatorcontrib><creatorcontrib>Büscher, Janine</creatorcontrib><creatorcontrib>Kurtz, Joachim</creatorcontrib><creatorcontrib>Scharsack, Jörn P.</creatorcontrib><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><collection>Immunology Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Fish & shellfish immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kutyrev, Ivan A.</au><au>Franke, Frederik</au><au>Büscher, Janine</au><au>Kurtz, Joachim</au><au>Scharsack, Jörn P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus</atitle><jtitle>Fish & shellfish immunology</jtitle><addtitle>Fish Shellfish Immunol</addtitle><date>2014-12</date><risdate>2014</risdate><volume>41</volume><issue>2</issue><spage>473</spage><epage>481</epage><pages>473-481</pages><issn>1050-4648</issn><eissn>1095-9947</eissn><abstract>Many helminth parasites have evolved strategies to evade the immune response of their hosts, which includes immunomodulation. Prostaglandin E2 (PGE2) is one of the best-described immunomodulators in mammalian helminth parasite infections. We hypothesized that also in teleost fish anti-helminthic immune responses are regulated via PGE2. We used a model system consisting of the tapeworm Schistocephalus solidus and its host, the three-spined stickleback (Gasterosteus aculeatus), to investigate in vitro effects of PGE2 on head kidney leucocytes (HKL) derived from sticklebacks that were experimentally infected with S. solidus. PGE2 was tested alone or in combination with either S. solidus antigens or bacterial lipopolysaccharides (LPS). After in vitro culture, cell viability and changes in leucocyte subpopulations (granulocytes to lymphocytes ratios) were monitored by flow cytometry and HKL were tested for their capacity to produce reactive oxygen species (ROS) with a chemiluminescence assay. In short term (2 h) HKL cultures PGE2 did not change the total numbers of live HKL, but the production of ROS decreased significantly with high (0.1 μmol L−1) PGE2 concentrations. In long-term (96 h) cultures high PGE2 concentrations induced a sharp decrease of leucocytes viability, while low (0.1 pmol L−1) and intermediate (0.1 nmol L−1) concentrations of PGE2 caused elevated leucocyte viability compared to controls. This coincided with reduced ROS production in cultures with high PGE2 and elevated ROS production in cultures with low PGE2. Granulocyte to lymphocyte ratios increased with high PGE2 concentrations alone and in combination with S. solidus antigens and LPS, most prominently with HKL from S. solidus infected sticklebacks. The present study supports the hypothesis that PGE2 might be an immunomodulator in tapeworm–fish parasite–host interactions.
[Display omitted]
•The highest concentration of PGE2 induced a sharp decrease of leucocytes viability.•Low concentrations of PGE2 caused increased leucocyte viability.•The highest concentration of PGE2 increased granulocyte to leucocyte ratios.•The highest concentration of PGE2 decreased reactive oxygen species activity.•PGE2 might be an immunomodulator in Cestode–fish parasite–host interactions.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>25301719</pmid><doi>10.1016/j.fsi.2014.09.031</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1050-4648 |
ispartof | Fish & shellfish immunology, 2014-12, Vol.41 (2), p.473-481 |
issn | 1050-4648 1095-9947 |
language | eng |
recordid | cdi_proquest_miscellaneous_1647008455 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Analysis of Variance Animals Cell Survival - drug effects Cestoda Cestoda - immunology Dinoprostone - immunology Dinoprostone - pharmacology Flow Cytometry Gasterosteus aculeatus Head Kidney - cytology In Vitro Techniques In vitro leucocyte responses Leukocytes - drug effects Leukocytes - immunology Lipopolysaccharides Parasite immunomodulation Prostaglandin E2 Reactive Oxygen Species - metabolism Schistocephalus solidus Smegmamorpha - immunology Smegmamorpha - parasitology Teleostei |
title | In vitro effects of prostaglandin E2 on leucocytes from sticklebacks (Gasterosteus aculeatus) infected and not infected with the cestode Schistocephalus solidus |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T04%3A19%3A26IST&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=In%C2%A0vitro%20effects%20of%20prostaglandin%20E2%20on%20leucocytes%20from%20sticklebacks%20(Gasterosteus%20aculeatus)%20infected%20and%20not%20infected%20with%20the%20cestode%20Schistocephalus%20solidus&rft.jtitle=Fish%20&%20shellfish%20immunology&rft.au=Kutyrev,%20Ivan%20A.&rft.date=2014-12&rft.volume=41&rft.issue=2&rft.spage=473&rft.epage=481&rft.pages=473-481&rft.issn=1050-4648&rft.eissn=1095-9947&rft_id=info:doi/10.1016/j.fsi.2014.09.031&rft_dat=%3Cproquest_cross%3E1647008455%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1629956727&rft_id=info:pmid/25301719&rft_els_id=S1050464814003660&rfr_iscdi=true |