Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech

In recent years, several studies have demonstrated that the RNASET2 gene is involved in the control of tumorigenicity in ovarian cancer cells. Furthermore, a role in establishing a functional cross-talk between cancer cells and the surrounding tumor microenvironment has been unveiled for this gene,...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell and tissue research 2017-05, Vol.368 (2), p.337-351
Hauptverfasser: Baranzini, Nicolò, Pedrini, Edoardo, Girardello, Rossana, Tettamanti, Gianluca, de Eguileor, Magda, Taramelli, Roberto, Acquati, Francesco, Grimaldi, Annalisa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 351
container_issue 2
container_start_page 337
container_title Cell and tissue research
container_volume 368
creator Baranzini, Nicolò
Pedrini, Edoardo
Girardello, Rossana
Tettamanti, Gianluca
de Eguileor, Magda
Taramelli, Roberto
Acquati, Francesco
Grimaldi, Annalisa
description In recent years, several studies have demonstrated that the RNASET2 gene is involved in the control of tumorigenicity in ovarian cancer cells. Furthermore, a role in establishing a functional cross-talk between cancer cells and the surrounding tumor microenvironment has been unveiled for this gene, based on its ability to act as an inducer of the innate immune response. Although several studies have reported on the molecular features of RNASET2, the details on the mechanisms by which this evolutionarily conserved ribonuclease regulates the immune system are still poorly defined. In the effort to clarify this aspect, we report here the effect of recombinant human RNASET2 injection and its role in regulating the innate immune response after bacterial challenge in an invertebrate model, the medicinal leech. We found that recombinant RNASET2 injection induces fibroplasias, connective tissue remodeling and the recruitment of numerous infiltrating cells expressing the specific macrophage markers CD68 and Hm AIF1. The RNASET2-mediated chemotactic activity for macrophages has been further confirmed by using a consolidated experimental approach based on injection of the Matrigel biomatrice (MG) supplemented with recombinant RNASET2 in the leech body wall. One week after injection, a large number of CD68 + and Hm AIF-1 + macrophages massively infiltrated MG sponges. Finally, in leeches challenged with lipopolysaccharides (LPS) or with the environmental bacteria pathogen Micrococcus nishinomiyaensis , numerous macrophages migrating to the site of inoculation expressed high levels of endogenous RNASET2. Taken together, these results suggest that RNASET2 is likely involved in the initial phase of the inflammatory response in leeches.
doi_str_mv 10.1007/s00441-016-2557-9
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1897371399</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A550951922</galeid><sourcerecordid>A550951922</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-124feced29e392f7102ffdb33497fd1f55b6133e7a6800b0603351b8b74feb533</originalsourceid><addsrcrecordid>eNqNklFrFDEUhYModq3-AF9kQBBfpt4kk8nkcSnVCkVBK_gWMpk7uykzyTqZKfTfe9et2oqCyUMg9zsn3JvD2HMOJxxAv8kAVcVL4HUplNKlecBWvJKihEY3D9kKJIhS1_XXI_Yk5ysAXtW1ecyORAMaaqlXLJ0vo4vFhD6NbYguzsWnD-vPZ5eiDLFbPHZFiP3gxtHNabohMO9SzFi42BU-xYh-DtdYzCHnBak8pg6HEDckK-YtFiN2wZPxUAyIfvuUPerdkPHZ7XnMvrw9uzw9Ly8-vnt_ur4ovQI5l1xUPdLjwqA0otccRN93rZSV0X3He6XamkuJ2tUNQAs1SKl427SadK2S8pi9PvjupvRtwTzbMWSPw-AipiVb3hgtNZfG_AeqCDVGNYS-_AO9SstEzf0wBFqc69_Uxg1oaXxpnpzfm9q1UmAUN0IQdfIXinaHY6DJYh_o_p7g1R3BFt0wb3MaljnQh9wH-QH0U8p5wt7upjC66cZysPvg2ENwLAXH7oNj90N4cdvZ0tKX_VL8TAoB4gBkKsUNTnda_6frd_cfyvI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1890000117</pqid></control><display><type>article</type><title>Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Baranzini, Nicolò ; Pedrini, Edoardo ; Girardello, Rossana ; Tettamanti, Gianluca ; de Eguileor, Magda ; Taramelli, Roberto ; Acquati, Francesco ; Grimaldi, Annalisa</creator><creatorcontrib>Baranzini, Nicolò ; Pedrini, Edoardo ; Girardello, Rossana ; Tettamanti, Gianluca ; de Eguileor, Magda ; Taramelli, Roberto ; Acquati, Francesco ; Grimaldi, Annalisa</creatorcontrib><description>In recent years, several studies have demonstrated that the RNASET2 gene is involved in the control of tumorigenicity in ovarian cancer cells. Furthermore, a role in establishing a functional cross-talk between cancer cells and the surrounding tumor microenvironment has been unveiled for this gene, based on its ability to act as an inducer of the innate immune response. Although several studies have reported on the molecular features of RNASET2, the details on the mechanisms by which this evolutionarily conserved ribonuclease regulates the immune system are still poorly defined. In the effort to clarify this aspect, we report here the effect of recombinant human RNASET2 injection and its role in regulating the innate immune response after bacterial challenge in an invertebrate model, the medicinal leech. We found that recombinant RNASET2 injection induces fibroplasias, connective tissue remodeling and the recruitment of numerous infiltrating cells expressing the specific macrophage markers CD68 and Hm AIF1. The RNASET2-mediated chemotactic activity for macrophages has been further confirmed by using a consolidated experimental approach based on injection of the Matrigel biomatrice (MG) supplemented with recombinant RNASET2 in the leech body wall. One week after injection, a large number of CD68 + and Hm AIF-1 + macrophages massively infiltrated MG sponges. Finally, in leeches challenged with lipopolysaccharides (LPS) or with the environmental bacteria pathogen Micrococcus nishinomiyaensis , numerous macrophages migrating to the site of inoculation expressed high levels of endogenous RNASET2. Taken together, these results suggest that RNASET2 is likely involved in the initial phase of the inflammatory response in leeches.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-016-2557-9</identifier><identifier>PMID: 28070637</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Acid Phosphatase - metabolism ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Cell Proliferation - drug effects ; Collagen - metabolism ; Connective Tissue - drug effects ; Connective Tissue - pathology ; Cryoultramicrotomy ; Drug Combinations ; Enzyme Assays ; Fluorescent Antibody Technique ; Genes ; Hirudinea ; Hirudo medicinalis - anatomy &amp; histology ; Hirudo medicinalis - drug effects ; Hirudo medicinalis - physiology ; Hirudo medicinalis - ultrastructure ; Human Genetics ; Humans ; Immune response ; Immune system ; Inflammation ; Inflammation - pathology ; Laminin - metabolism ; Lipopolysaccharides - pharmacology ; Macrophages - drug effects ; Macrophages - metabolism ; Micrococcus ; Molecular Medicine ; Ovarian cancer ; Proteoglycans - metabolism ; Proteomics ; Recombinant Proteins - pharmacology ; Regular Article ; Ribonuclease ; Ribonucleases - pharmacology ; Tumor Suppressor Proteins - pharmacology ; Worms</subject><ispartof>Cell and tissue research, 2017-05, Vol.368 (2), p.337-351</ispartof><rights>Springer-Verlag Berlin Heidelberg 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Cell and Tissue Research is a copyright of Springer, 2017.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-124feced29e392f7102ffdb33497fd1f55b6133e7a6800b0603351b8b74feb533</citedby><cites>FETCH-LOGICAL-c503t-124feced29e392f7102ffdb33497fd1f55b6133e7a6800b0603351b8b74feb533</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-016-2557-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-016-2557-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28070637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baranzini, Nicolò</creatorcontrib><creatorcontrib>Pedrini, Edoardo</creatorcontrib><creatorcontrib>Girardello, Rossana</creatorcontrib><creatorcontrib>Tettamanti, Gianluca</creatorcontrib><creatorcontrib>de Eguileor, Magda</creatorcontrib><creatorcontrib>Taramelli, Roberto</creatorcontrib><creatorcontrib>Acquati, Francesco</creatorcontrib><creatorcontrib>Grimaldi, Annalisa</creatorcontrib><title>Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>In recent years, several studies have demonstrated that the RNASET2 gene is involved in the control of tumorigenicity in ovarian cancer cells. Furthermore, a role in establishing a functional cross-talk between cancer cells and the surrounding tumor microenvironment has been unveiled for this gene, based on its ability to act as an inducer of the innate immune response. Although several studies have reported on the molecular features of RNASET2, the details on the mechanisms by which this evolutionarily conserved ribonuclease regulates the immune system are still poorly defined. In the effort to clarify this aspect, we report here the effect of recombinant human RNASET2 injection and its role in regulating the innate immune response after bacterial challenge in an invertebrate model, the medicinal leech. We found that recombinant RNASET2 injection induces fibroplasias, connective tissue remodeling and the recruitment of numerous infiltrating cells expressing the specific macrophage markers CD68 and Hm AIF1. The RNASET2-mediated chemotactic activity for macrophages has been further confirmed by using a consolidated experimental approach based on injection of the Matrigel biomatrice (MG) supplemented with recombinant RNASET2 in the leech body wall. One week after injection, a large number of CD68 + and Hm AIF-1 + macrophages massively infiltrated MG sponges. Finally, in leeches challenged with lipopolysaccharides (LPS) or with the environmental bacteria pathogen Micrococcus nishinomiyaensis , numerous macrophages migrating to the site of inoculation expressed high levels of endogenous RNASET2. Taken together, these results suggest that RNASET2 is likely involved in the initial phase of the inflammatory response in leeches.</description><subject>Acid Phosphatase - metabolism</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Proliferation - drug effects</subject><subject>Collagen - metabolism</subject><subject>Connective Tissue - drug effects</subject><subject>Connective Tissue - pathology</subject><subject>Cryoultramicrotomy</subject><subject>Drug Combinations</subject><subject>Enzyme Assays</subject><subject>Fluorescent Antibody Technique</subject><subject>Genes</subject><subject>Hirudinea</subject><subject>Hirudo medicinalis - anatomy &amp; histology</subject><subject>Hirudo medicinalis - drug effects</subject><subject>Hirudo medicinalis - physiology</subject><subject>Hirudo medicinalis - ultrastructure</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>Inflammation - pathology</subject><subject>Laminin - metabolism</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Micrococcus</subject><subject>Molecular Medicine</subject><subject>Ovarian cancer</subject><subject>Proteoglycans - metabolism</subject><subject>Proteomics</subject><subject>Recombinant Proteins - pharmacology</subject><subject>Regular Article</subject><subject>Ribonuclease</subject><subject>Ribonucleases - pharmacology</subject><subject>Tumor Suppressor Proteins - pharmacology</subject><subject>Worms</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNklFrFDEUhYModq3-AF9kQBBfpt4kk8nkcSnVCkVBK_gWMpk7uykzyTqZKfTfe9et2oqCyUMg9zsn3JvD2HMOJxxAv8kAVcVL4HUplNKlecBWvJKihEY3D9kKJIhS1_XXI_Yk5ysAXtW1ecyORAMaaqlXLJ0vo4vFhD6NbYguzsWnD-vPZ5eiDLFbPHZFiP3gxtHNabohMO9SzFi42BU-xYh-DtdYzCHnBak8pg6HEDckK-YtFiN2wZPxUAyIfvuUPerdkPHZ7XnMvrw9uzw9Ly8-vnt_ur4ovQI5l1xUPdLjwqA0otccRN93rZSV0X3He6XamkuJ2tUNQAs1SKl427SadK2S8pi9PvjupvRtwTzbMWSPw-AipiVb3hgtNZfG_AeqCDVGNYS-_AO9SstEzf0wBFqc69_Uxg1oaXxpnpzfm9q1UmAUN0IQdfIXinaHY6DJYh_o_p7g1R3BFt0wb3MaljnQh9wH-QH0U8p5wt7upjC66cZysPvg2ENwLAXH7oNj90N4cdvZ0tKX_VL8TAoB4gBkKsUNTnda_6frd_cfyvI</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Baranzini, Nicolò</creator><creator>Pedrini, Edoardo</creator><creator>Girardello, Rossana</creator><creator>Tettamanti, Gianluca</creator><creator>de Eguileor, Magda</creator><creator>Taramelli, Roberto</creator><creator>Acquati, Francesco</creator><creator>Grimaldi, Annalisa</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20170501</creationdate><title>Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech</title><author>Baranzini, Nicolò ; Pedrini, Edoardo ; Girardello, Rossana ; Tettamanti, Gianluca ; de Eguileor, Magda ; Taramelli, Roberto ; Acquati, Francesco ; Grimaldi, Annalisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-124feced29e392f7102ffdb33497fd1f55b6133e7a6800b0603351b8b74feb533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Acid Phosphatase - metabolism</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Proliferation - drug effects</topic><topic>Collagen - metabolism</topic><topic>Connective Tissue - drug effects</topic><topic>Connective Tissue - pathology</topic><topic>Cryoultramicrotomy</topic><topic>Drug Combinations</topic><topic>Enzyme Assays</topic><topic>Fluorescent Antibody Technique</topic><topic>Genes</topic><topic>Hirudinea</topic><topic>Hirudo medicinalis - anatomy &amp; histology</topic><topic>Hirudo medicinalis - drug effects</topic><topic>Hirudo medicinalis - physiology</topic><topic>Hirudo medicinalis - ultrastructure</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Inflammation</topic><topic>Inflammation - pathology</topic><topic>Laminin - metabolism</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Micrococcus</topic><topic>Molecular Medicine</topic><topic>Ovarian cancer</topic><topic>Proteoglycans - metabolism</topic><topic>Proteomics</topic><topic>Recombinant Proteins - pharmacology</topic><topic>Regular Article</topic><topic>Ribonuclease</topic><topic>Ribonucleases - pharmacology</topic><topic>Tumor Suppressor Proteins - pharmacology</topic><topic>Worms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baranzini, Nicolò</creatorcontrib><creatorcontrib>Pedrini, Edoardo</creatorcontrib><creatorcontrib>Girardello, Rossana</creatorcontrib><creatorcontrib>Tettamanti, Gianluca</creatorcontrib><creatorcontrib>de Eguileor, Magda</creatorcontrib><creatorcontrib>Taramelli, Roberto</creatorcontrib><creatorcontrib>Acquati, Francesco</creatorcontrib><creatorcontrib>Grimaldi, Annalisa</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baranzini, Nicolò</au><au>Pedrini, Edoardo</au><au>Girardello, Rossana</au><au>Tettamanti, Gianluca</au><au>de Eguileor, Magda</au><au>Taramelli, Roberto</au><au>Acquati, Francesco</au><au>Grimaldi, Annalisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>368</volume><issue>2</issue><spage>337</spage><epage>351</epage><pages>337-351</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>In recent years, several studies have demonstrated that the RNASET2 gene is involved in the control of tumorigenicity in ovarian cancer cells. Furthermore, a role in establishing a functional cross-talk between cancer cells and the surrounding tumor microenvironment has been unveiled for this gene, based on its ability to act as an inducer of the innate immune response. Although several studies have reported on the molecular features of RNASET2, the details on the mechanisms by which this evolutionarily conserved ribonuclease regulates the immune system are still poorly defined. In the effort to clarify this aspect, we report here the effect of recombinant human RNASET2 injection and its role in regulating the innate immune response after bacterial challenge in an invertebrate model, the medicinal leech. We found that recombinant RNASET2 injection induces fibroplasias, connective tissue remodeling and the recruitment of numerous infiltrating cells expressing the specific macrophage markers CD68 and Hm AIF1. The RNASET2-mediated chemotactic activity for macrophages has been further confirmed by using a consolidated experimental approach based on injection of the Matrigel biomatrice (MG) supplemented with recombinant RNASET2 in the leech body wall. One week after injection, a large number of CD68 + and Hm AIF-1 + macrophages massively infiltrated MG sponges. Finally, in leeches challenged with lipopolysaccharides (LPS) or with the environmental bacteria pathogen Micrococcus nishinomiyaensis , numerous macrophages migrating to the site of inoculation expressed high levels of endogenous RNASET2. Taken together, these results suggest that RNASET2 is likely involved in the initial phase of the inflammatory response in leeches.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28070637</pmid><doi>10.1007/s00441-016-2557-9</doi><tpages>15</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0302-766X
ispartof Cell and tissue research, 2017-05, Vol.368 (2), p.337-351
issn 0302-766X
1432-0878
language eng
recordid cdi_proquest_miscellaneous_1897371399
source MEDLINE; Springer Nature - Complete Springer Journals
subjects Acid Phosphatase - metabolism
Animals
Biomedical and Life Sciences
Biomedicine
Cell Proliferation - drug effects
Collagen - metabolism
Connective Tissue - drug effects
Connective Tissue - pathology
Cryoultramicrotomy
Drug Combinations
Enzyme Assays
Fluorescent Antibody Technique
Genes
Hirudinea
Hirudo medicinalis - anatomy & histology
Hirudo medicinalis - drug effects
Hirudo medicinalis - physiology
Hirudo medicinalis - ultrastructure
Human Genetics
Humans
Immune response
Immune system
Inflammation
Inflammation - pathology
Laminin - metabolism
Lipopolysaccharides - pharmacology
Macrophages - drug effects
Macrophages - metabolism
Micrococcus
Molecular Medicine
Ovarian cancer
Proteoglycans - metabolism
Proteomics
Recombinant Proteins - pharmacology
Regular Article
Ribonuclease
Ribonucleases - pharmacology
Tumor Suppressor Proteins - pharmacology
Worms
title Human recombinant RNASET2-induced inflammatory response and connective tissue remodeling in the medicinal leech
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T22%3A01%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Human%20recombinant%20RNASET2-induced%20inflammatory%20response%20and%20connective%20tissue%20remodeling%20in%20the%20medicinal%20leech&rft.jtitle=Cell%20and%20tissue%20research&rft.au=Baranzini,%20Nicol%C3%B2&rft.date=2017-05-01&rft.volume=368&rft.issue=2&rft.spage=337&rft.epage=351&rft.pages=337-351&rft.issn=0302-766X&rft.eissn=1432-0878&rft_id=info:doi/10.1007/s00441-016-2557-9&rft_dat=%3Cgale_proqu%3EA550951922%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1890000117&rft_id=info:pmid/28070637&rft_galeid=A550951922&rfr_iscdi=true