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PS integrins and laminins: key regulators of cell migration during Drosophila embryogenesis
During embryonic development, there are numerous cases where organ or tissue formation depends upon the migration of primordial cells. In the Drosophila embryo, the visceral mesoderm (vm) acts as a substrate for the migration of several cell populations of epithelial origin, including the endoderm,...
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Published in: | PloS one 2011-09, Vol.6 (9), p.e23893-e23893 |
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description | During embryonic development, there are numerous cases where organ or tissue formation depends upon the migration of primordial cells. In the Drosophila embryo, the visceral mesoderm (vm) acts as a substrate for the migration of several cell populations of epithelial origin, including the endoderm, the trachea and the salivary glands. These migratory processes require both integrins and laminins. The current model is that αPS1βPS (PS1) and/or αPS3βPS (PS3) integrins are required in migrating cells, whereas αPS2βPS (PS2) integrin is required in the vm, where it performs an as yet unidentified function. Here, we show that PS1 integrins are also required for the migration over the vm of cells of mesodermal origin, the caudal visceral mesoderm (CVM). These results support a model in which PS1 might have evolved to acquire the migratory function of integrins, irrespective of the origin of the tissue. This integrin function is highly specific and its specificity resides mainly in the extracellular domain. In addition, we have identified the Laminin α1,2 trimer, as the key extracellular matrix (ECM) component regulating CVM migration. Furthermore, we show that, as it is the case in vertebrates, integrins, and specifically PS2, contributes to CVM movement by participating in the correct assembly of the ECM that serves as tracks for migration. |
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In the Drosophila embryo, the visceral mesoderm (vm) acts as a substrate for the migration of several cell populations of epithelial origin, including the endoderm, the trachea and the salivary glands. These migratory processes require both integrins and laminins. The current model is that αPS1βPS (PS1) and/or αPS3βPS (PS3) integrins are required in migrating cells, whereas αPS2βPS (PS2) integrin is required in the vm, where it performs an as yet unidentified function. Here, we show that PS1 integrins are also required for the migration over the vm of cells of mesodermal origin, the caudal visceral mesoderm (CVM). These results support a model in which PS1 might have evolved to acquire the migratory function of integrins, irrespective of the origin of the tissue. This integrin function is highly specific and its specificity resides mainly in the extracellular domain. In addition, we have identified the Laminin α1,2 trimer, as the key extracellular matrix (ECM) component regulating CVM migration. Furthermore, we show that, as it is the case in vertebrates, integrins, and specifically PS2, contributes to CVM movement by participating in the correct assembly of the ECM that serves as tracks for migration.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0023893</identifier><identifier>PMID: 21949686</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Animals, Genetically Modified ; Biology ; Cell adhesion & migration ; Cell migration ; Cell Movement ; Drosophila ; Drosophila - embryology ; Drosophila - genetics ; Drosophila - metabolism ; Drosophila melanogaster ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Embryo, Nonmammalian - cytology ; Embryo, Nonmammalian - embryology ; Embryo, Nonmammalian - metabolism ; Embryogenesis ; Embryonic development ; Embryonic growth stage ; Embryos ; Endoderm ; Extracellular matrix ; Gene expression ; Glands ; Green Fluorescent Proteins - genetics ; Green Fluorescent Proteins - metabolism ; In Situ Hybridization ; Insects ; Integrins ; Integrins - genetics ; Integrins - metabolism ; Kinases ; Laminin ; Laminin - genetics ; Laminin - metabolism ; Mammals ; Mesoderm ; Mesoderm - cytology ; Mesoderm - embryology ; Mesoderm - metabolism ; Microscopy, Confocal ; Morphogenesis ; Mutation ; Presenilin 1 ; Presenilin 2 ; Regulators ; Salivary glands ; Time-Lapse Imaging ; Trachea ; Vertebrates</subject><ispartof>PloS one, 2011-09, Vol.6 (9), p.e23893-e23893</ispartof><rights>COPYRIGHT 2011 Public Library of Science</rights><rights>2011 Urbano et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Urbano et al. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c691t-98b2f3fcf9d18aa527f86621fd1a82aa23902db30d46da4c5db0901eceb503fe3</citedby><cites>FETCH-LOGICAL-c691t-98b2f3fcf9d18aa527f86621fd1a82aa23902db30d46da4c5db0901eceb503fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1308735257/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1308735257?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21949686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gonzalez, Cayetano</contributor><creatorcontrib>Urbano, Jose M</creatorcontrib><creatorcontrib>Domínguez-Giménez, Paloma</creatorcontrib><creatorcontrib>Estrada, Beatriz</creatorcontrib><creatorcontrib>Martín-Bermudo, María D</creatorcontrib><title>PS integrins and laminins: key regulators of cell migration during Drosophila embryogenesis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>During embryonic development, there are numerous cases where organ or tissue formation depends upon the migration of primordial cells. In the Drosophila embryo, the visceral mesoderm (vm) acts as a substrate for the migration of several cell populations of epithelial origin, including the endoderm, the trachea and the salivary glands. These migratory processes require both integrins and laminins. The current model is that αPS1βPS (PS1) and/or αPS3βPS (PS3) integrins are required in migrating cells, whereas αPS2βPS (PS2) integrin is required in the vm, where it performs an as yet unidentified function. Here, we show that PS1 integrins are also required for the migration over the vm of cells of mesodermal origin, the caudal visceral mesoderm (CVM). These results support a model in which PS1 might have evolved to acquire the migratory function of integrins, irrespective of the origin of the tissue. This integrin function is highly specific and its specificity resides mainly in the extracellular domain. 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In the Drosophila embryo, the visceral mesoderm (vm) acts as a substrate for the migration of several cell populations of epithelial origin, including the endoderm, the trachea and the salivary glands. These migratory processes require both integrins and laminins. The current model is that αPS1βPS (PS1) and/or αPS3βPS (PS3) integrins are required in migrating cells, whereas αPS2βPS (PS2) integrin is required in the vm, where it performs an as yet unidentified function. Here, we show that PS1 integrins are also required for the migration over the vm of cells of mesodermal origin, the caudal visceral mesoderm (CVM). These results support a model in which PS1 might have evolved to acquire the migratory function of integrins, irrespective of the origin of the tissue. This integrin function is highly specific and its specificity resides mainly in the extracellular domain. In addition, we have identified the Laminin α1,2 trimer, as the key extracellular matrix (ECM) component regulating CVM migration. Furthermore, we show that, as it is the case in vertebrates, integrins, and specifically PS2, contributes to CVM movement by participating in the correct assembly of the ECM that serves as tracks for migration.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>21949686</pmid><doi>10.1371/journal.pone.0023893</doi><tpages>e23893</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Animals, Genetically Modified Biology Cell adhesion & migration Cell migration Cell Movement Drosophila Drosophila - embryology Drosophila - genetics Drosophila - metabolism Drosophila melanogaster Drosophila Proteins - genetics Drosophila Proteins - metabolism Embryo, Nonmammalian - cytology Embryo, Nonmammalian - embryology Embryo, Nonmammalian - metabolism Embryogenesis Embryonic development Embryonic growth stage Embryos Endoderm Extracellular matrix Gene expression Glands Green Fluorescent Proteins - genetics Green Fluorescent Proteins - metabolism In Situ Hybridization Insects Integrins Integrins - genetics Integrins - metabolism Kinases Laminin Laminin - genetics Laminin - metabolism Mammals Mesoderm Mesoderm - cytology Mesoderm - embryology Mesoderm - metabolism Microscopy, Confocal Morphogenesis Mutation Presenilin 1 Presenilin 2 Regulators Salivary glands Time-Lapse Imaging Trachea Vertebrates |
title | PS integrins and laminins: key regulators of cell migration during Drosophila embryogenesis |
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