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,...
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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 |
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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 & 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 & 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 & 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 & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & 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> |
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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 |
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