New insights into Drosophila larval haemocyte functions through genome‐wide analysis
Summary Drosophila blood cells or haemocytes comprise three cell lineages, plasmatocytes, crystal cells and lamellocytes, involved in immune functions such as phagocytosis, melanisation and encapsulation. Transcriptional profiling of activities of distinct haemocyte populations and from naïve or inf...
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Veröffentlicht in: | Cellular microbiology 2005-03, Vol.7 (3), p.335-350 |
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creator | Irving, Phil Ubeda, Jean‐Michel Doucet, Daniel Troxler, Laurent Lagueux, Marie Zachary, Daniel Hoffmann, Jules A. Hetru, Charles Meister, Marie |
description | Summary
Drosophila blood cells or haemocytes comprise three cell lineages, plasmatocytes, crystal cells and lamellocytes, involved in immune functions such as phagocytosis, melanisation and encapsulation. Transcriptional profiling of activities of distinct haemocyte populations and from naïve or infected larvae, was performed to find genes contributing to haemocyte functions. Of the 13 000 genes represented on the microarray, over 2500 exhibited significantly enriched transcription in haemocytes. Among these were genes encoding integrins, peptidoglycan recognition proteins (PGRPs), scavenger receptors, lectins, cell adhesion molecules and serine proteases. One relevant outcome of this analysis was the gain of new insights into the lamellocyte encapsulation process. We showed that lamellocytes require βPS integrin for encapsulation and that they transcribe one prophenoloxidase gene enabling them to produce the enzyme necessary for melanisation of the capsule. A second compelling observation was that following infection, the gene encoding the cytokine Spätzle was uniquely upregulated in haemocytes and not the fat body. This shows that Drosophila haemocytes produce a signal molecule ready to be activated through cleavage after pathogen recognition, informing distant tissues of infection. |
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Drosophila blood cells or haemocytes comprise three cell lineages, plasmatocytes, crystal cells and lamellocytes, involved in immune functions such as phagocytosis, melanisation and encapsulation. Transcriptional profiling of activities of distinct haemocyte populations and from naïve or infected larvae, was performed to find genes contributing to haemocyte functions. Of the 13 000 genes represented on the microarray, over 2500 exhibited significantly enriched transcription in haemocytes. Among these were genes encoding integrins, peptidoglycan recognition proteins (PGRPs), scavenger receptors, lectins, cell adhesion molecules and serine proteases. One relevant outcome of this analysis was the gain of new insights into the lamellocyte encapsulation process. We showed that lamellocytes require βPS integrin for encapsulation and that they transcribe one prophenoloxidase gene enabling them to produce the enzyme necessary for melanisation of the capsule. A second compelling observation was that following infection, the gene encoding the cytokine Spätzle was uniquely upregulated in haemocytes and not the fat body. This shows that Drosophila haemocytes produce a signal molecule ready to be activated through cleavage after pathogen recognition, informing distant tissues of infection.</description><identifier>ISSN: 1462-5814</identifier><identifier>EISSN: 1462-5822</identifier><identifier>DOI: 10.1111/j.1462-5822.2004.00462.x</identifier><identifier>PMID: 15679837</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Animals ; Biochemistry, Molecular Biology ; Catechol Oxidase - genetics ; Catechol Oxidase - metabolism ; Cell Lineage ; Cellular Biology ; Drosophila - genetics ; Drosophila - immunology ; Drosophila - microbiology ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Enzyme Precursors - genetics ; Enzyme Precursors - metabolism ; Escherichia coli - pathogenicity ; Fat Body - metabolism ; Fat Body - microbiology ; Gene Expression Profiling ; Genome ; Hemocytes - immunology ; Hemocytes - metabolism ; Hemocytes - microbiology ; Integrin alpha Chains ; Integrins - genetics ; Integrins - metabolism ; Larva - genetics ; Larva - immunology ; Larva - microbiology ; Life Sciences ; Micrococcus luteus - pathogenicity ; Molecular biology</subject><ispartof>Cellular microbiology, 2005-03, Vol.7 (3), p.335-350</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4002-c6ff324218f2cd9cf7b9dd0ef3cca35154508d813cde9ab028465a05f7ece4663</citedby><cites>FETCH-LOGICAL-c4002-c6ff324218f2cd9cf7b9dd0ef3cca35154508d813cde9ab028465a05f7ece4663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1462-5822.2004.00462.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1462-5822.2004.00462.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15679837$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00093694$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Irving, Phil</creatorcontrib><creatorcontrib>Ubeda, Jean‐Michel</creatorcontrib><creatorcontrib>Doucet, Daniel</creatorcontrib><creatorcontrib>Troxler, Laurent</creatorcontrib><creatorcontrib>Lagueux, Marie</creatorcontrib><creatorcontrib>Zachary, Daniel</creatorcontrib><creatorcontrib>Hoffmann, Jules A.</creatorcontrib><creatorcontrib>Hetru, Charles</creatorcontrib><creatorcontrib>Meister, Marie</creatorcontrib><title>New insights into Drosophila larval haemocyte functions through genome‐wide analysis</title><title>Cellular microbiology</title><addtitle>Cell Microbiol</addtitle><description>Summary
Drosophila blood cells or haemocytes comprise three cell lineages, plasmatocytes, crystal cells and lamellocytes, involved in immune functions such as phagocytosis, melanisation and encapsulation. Transcriptional profiling of activities of distinct haemocyte populations and from naïve or infected larvae, was performed to find genes contributing to haemocyte functions. Of the 13 000 genes represented on the microarray, over 2500 exhibited significantly enriched transcription in haemocytes. Among these were genes encoding integrins, peptidoglycan recognition proteins (PGRPs), scavenger receptors, lectins, cell adhesion molecules and serine proteases. One relevant outcome of this analysis was the gain of new insights into the lamellocyte encapsulation process. We showed that lamellocytes require βPS integrin for encapsulation and that they transcribe one prophenoloxidase gene enabling them to produce the enzyme necessary for melanisation of the capsule. A second compelling observation was that following infection, the gene encoding the cytokine Spätzle was uniquely upregulated in haemocytes and not the fat body. This shows that Drosophila haemocytes produce a signal molecule ready to be activated through cleavage after pathogen recognition, informing distant tissues of infection.</description><subject>Animals</subject><subject>Biochemistry, Molecular Biology</subject><subject>Catechol Oxidase - genetics</subject><subject>Catechol Oxidase - metabolism</subject><subject>Cell Lineage</subject><subject>Cellular Biology</subject><subject>Drosophila - genetics</subject><subject>Drosophila - immunology</subject><subject>Drosophila - microbiology</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Enzyme Precursors - genetics</subject><subject>Enzyme Precursors - metabolism</subject><subject>Escherichia coli - pathogenicity</subject><subject>Fat Body - metabolism</subject><subject>Fat Body - microbiology</subject><subject>Gene Expression Profiling</subject><subject>Genome</subject><subject>Hemocytes - immunology</subject><subject>Hemocytes - metabolism</subject><subject>Hemocytes - microbiology</subject><subject>Integrin alpha Chains</subject><subject>Integrins - genetics</subject><subject>Integrins - metabolism</subject><subject>Larva - genetics</subject><subject>Larva - immunology</subject><subject>Larva - microbiology</subject><subject>Life Sciences</subject><subject>Micrococcus luteus - pathogenicity</subject><subject>Molecular biology</subject><issn>1462-5814</issn><issn>1462-5822</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkN1q2zAYhsXYWP92C0VHgx3E1Z9lGXpSsq0tZNvJulOhyJ9iBdnKLLtpznYJvcZeSe0lZKcTCL1Iz_cKHoQwJRkd19U6o0KyWa4YyxghIhu3ZNnTG3R6fHh7zFScoLOU1oRQWVD6Hp3QXBal4sUp-vUdtti3ya_qPo2hj_hzF1Pc1D4YHEz3aAKuDTTR7nrAbmht72ObcF93cVjVeAVtbODlz_PWV4BNa8Iu-XSB3jkTEnw4nOfo4euXn_O72eLH7f38ZjGzghA2s9I5zgSjyjFbldYVy7KqCDhureE5zUVOVKUotxWUZkmYEjI3JHcFWBBS8nP0ad9bm6A3nW9Mt9PReH13s9DTHSGk5LIUj3RkP-7ZTRd_D5B63fhkIQTTQhySlgVXJVVTqdqDdjSROnDHZkr05F-v9aRWT5r15F__9a-fxtHLwx_DsoHq3-BB-Ahc74GtD7D772I9_3Y_Bv4KdGWVSg</recordid><startdate>200503</startdate><enddate>200503</enddate><creator>Irving, Phil</creator><creator>Ubeda, Jean‐Michel</creator><creator>Doucet, Daniel</creator><creator>Troxler, Laurent</creator><creator>Lagueux, Marie</creator><creator>Zachary, Daniel</creator><creator>Hoffmann, Jules A.</creator><creator>Hetru, Charles</creator><creator>Meister, Marie</creator><general>Blackwell Science Ltd</general><general>Wiley</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>1XC</scope></search><sort><creationdate>200503</creationdate><title>New insights into Drosophila larval haemocyte functions through genome‐wide analysis</title><author>Irving, Phil ; Ubeda, Jean‐Michel ; Doucet, Daniel ; Troxler, Laurent ; Lagueux, Marie ; Zachary, Daniel ; Hoffmann, Jules A. ; Hetru, Charles ; Meister, Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4002-c6ff324218f2cd9cf7b9dd0ef3cca35154508d813cde9ab028465a05f7ece4663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Biochemistry, Molecular Biology</topic><topic>Catechol Oxidase - genetics</topic><topic>Catechol Oxidase - metabolism</topic><topic>Cell Lineage</topic><topic>Cellular Biology</topic><topic>Drosophila - genetics</topic><topic>Drosophila - immunology</topic><topic>Drosophila - microbiology</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Enzyme Precursors - genetics</topic><topic>Enzyme Precursors - metabolism</topic><topic>Escherichia coli - pathogenicity</topic><topic>Fat Body - metabolism</topic><topic>Fat Body - microbiology</topic><topic>Gene Expression Profiling</topic><topic>Genome</topic><topic>Hemocytes - immunology</topic><topic>Hemocytes - metabolism</topic><topic>Hemocytes - microbiology</topic><topic>Integrin alpha Chains</topic><topic>Integrins - genetics</topic><topic>Integrins - metabolism</topic><topic>Larva - genetics</topic><topic>Larva - immunology</topic><topic>Larva - microbiology</topic><topic>Life Sciences</topic><topic>Micrococcus luteus - pathogenicity</topic><topic>Molecular biology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Irving, Phil</creatorcontrib><creatorcontrib>Ubeda, Jean‐Michel</creatorcontrib><creatorcontrib>Doucet, Daniel</creatorcontrib><creatorcontrib>Troxler, Laurent</creatorcontrib><creatorcontrib>Lagueux, Marie</creatorcontrib><creatorcontrib>Zachary, Daniel</creatorcontrib><creatorcontrib>Hoffmann, Jules A.</creatorcontrib><creatorcontrib>Hetru, Charles</creatorcontrib><creatorcontrib>Meister, Marie</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>Hyper Article en Ligne (HAL)</collection><jtitle>Cellular microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Irving, Phil</au><au>Ubeda, Jean‐Michel</au><au>Doucet, Daniel</au><au>Troxler, Laurent</au><au>Lagueux, Marie</au><au>Zachary, Daniel</au><au>Hoffmann, Jules A.</au><au>Hetru, Charles</au><au>Meister, Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New insights into Drosophila larval haemocyte functions through genome‐wide analysis</atitle><jtitle>Cellular microbiology</jtitle><addtitle>Cell Microbiol</addtitle><date>2005-03</date><risdate>2005</risdate><volume>7</volume><issue>3</issue><spage>335</spage><epage>350</epage><pages>335-350</pages><issn>1462-5814</issn><eissn>1462-5822</eissn><abstract>Summary
Drosophila blood cells or haemocytes comprise three cell lineages, plasmatocytes, crystal cells and lamellocytes, involved in immune functions such as phagocytosis, melanisation and encapsulation. Transcriptional profiling of activities of distinct haemocyte populations and from naïve or infected larvae, was performed to find genes contributing to haemocyte functions. Of the 13 000 genes represented on the microarray, over 2500 exhibited significantly enriched transcription in haemocytes. Among these were genes encoding integrins, peptidoglycan recognition proteins (PGRPs), scavenger receptors, lectins, cell adhesion molecules and serine proteases. One relevant outcome of this analysis was the gain of new insights into the lamellocyte encapsulation process. We showed that lamellocytes require βPS integrin for encapsulation and that they transcribe one prophenoloxidase gene enabling them to produce the enzyme necessary for melanisation of the capsule. A second compelling observation was that following infection, the gene encoding the cytokine Spätzle was uniquely upregulated in haemocytes and not the fat body. This shows that Drosophila haemocytes produce a signal molecule ready to be activated through cleavage after pathogen recognition, informing distant tissues of infection.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15679837</pmid><doi>10.1111/j.1462-5822.2004.00462.x</doi><tpages>16</tpages></addata></record> |
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subjects | Animals Biochemistry, Molecular Biology Catechol Oxidase - genetics Catechol Oxidase - metabolism Cell Lineage Cellular Biology Drosophila - genetics Drosophila - immunology Drosophila - microbiology Drosophila Proteins - genetics Drosophila Proteins - metabolism Enzyme Precursors - genetics Enzyme Precursors - metabolism Escherichia coli - pathogenicity Fat Body - metabolism Fat Body - microbiology Gene Expression Profiling Genome Hemocytes - immunology Hemocytes - metabolism Hemocytes - microbiology Integrin alpha Chains Integrins - genetics Integrins - metabolism Larva - genetics Larva - immunology Larva - microbiology Life Sciences Micrococcus luteus - pathogenicity Molecular biology |
title | New insights into Drosophila larval haemocyte functions through genome‐wide analysis |
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