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Pak1 regulates the orientation of apical polarization and lumen formation by distinct pathways
The development of the basic architecture of branching tubules enclosing a central lumen that characterizes most epithelial organs crucially depends on the apico-basolateral polarization of epithelial cells. Signals from the extracellular matrix control the orientation of the apical surface, so that...
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Published in: | PloS one 2012-07, Vol.7 (7), p.e41039 |
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description | The development of the basic architecture of branching tubules enclosing a central lumen that characterizes most epithelial organs crucially depends on the apico-basolateral polarization of epithelial cells. Signals from the extracellular matrix control the orientation of the apical surface, so that it faces the lumen interior, opposite to cell-matrix adhesion sites. This orientation of the apical surface is thought to be intrinsically linked to the formation of single lumens. We previously demonstrated in three-dimensional cyst cultures of Madin-Darby canine kidney (MDCK) cells that signaling by β1 integrins regulates the orientation of the apical surface, via a mechanism that depends on the activity of the small GTPase Rac1. Here, we investigated whether the Rac1 effector Pak1 is a downstream effector in this pathway. Expression of constitutive active Pak1 phenocopies the effect of β1 integrin inhibition in that it misorients the apical surface and induces a multilumen phenotype. The misorientation of apical surfaces depends on the interaction of active Pak1 with PIX proteins and is linked to defects in basement membrane assembly. In contrast, the multilumen phenotype was independent of PIX and the basement membrane. Therefore, Pak1 likely regulates apical polarization and lumen formation by two distinct pathways. |
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Signals from the extracellular matrix control the orientation of the apical surface, so that it faces the lumen interior, opposite to cell-matrix adhesion sites. This orientation of the apical surface is thought to be intrinsically linked to the formation of single lumens. We previously demonstrated in three-dimensional cyst cultures of Madin-Darby canine kidney (MDCK) cells that signaling by β1 integrins regulates the orientation of the apical surface, via a mechanism that depends on the activity of the small GTPase Rac1. Here, we investigated whether the Rac1 effector Pak1 is a downstream effector in this pathway. Expression of constitutive active Pak1 phenocopies the effect of β1 integrin inhibition in that it misorients the apical surface and induces a multilumen phenotype. The misorientation of apical surfaces depends on the interaction of active Pak1 with PIX proteins and is linked to defects in basement membrane assembly. In contrast, the multilumen phenotype was independent of PIX and the basement membrane. Therefore, Pak1 likely regulates apical polarization and lumen formation by two distinct pathways.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0041039</identifier><identifier>PMID: 22815903</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Biology ; Biotinylation ; Cancer ; Cell adhesion & migration ; Cell Line ; Cell Polarity - physiology ; Cell-Matrix Junctions ; Cysts ; Dogs ; Drosophila ; Epithelial cells ; Extracellular matrix ; Extracellular Matrix - metabolism ; Gene Expression Regulation ; Genotype & phenotype ; GTP Phosphohydrolases - metabolism ; Guanosine triphosphatases ; Guanosinetriphosphatase ; Homeostasis ; Immunoglobulins ; Insects ; Integrin beta1 - metabolism ; Integrins ; Kinases ; Lumens ; Microscopy, Confocal - methods ; Misalignment ; Models, Biological ; Morphogenesis ; Organs ; Orientation ; p21-Activated Kinases - metabolism ; Pathways ; Phenotype ; Phosphorylation ; Polarization ; Proteins ; Rac1 protein ; RNA, Small Interfering - metabolism ; Signaling ; Surgery ; Trypsin - chemistry ; Tubules</subject><ispartof>PloS one, 2012-07, Vol.7 (7), p.e41039</ispartof><rights>COPYRIGHT 2012 Public Library of Science</rights><rights>2012 deLeon 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>deLeon et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-643ead6f1307096b9ea77144ff7cc6282248c1eb00ce246467fbfa49c2315c1a3</citedby><cites>FETCH-LOGICAL-c692t-643ead6f1307096b9ea77144ff7cc6282248c1eb00ce246467fbfa49c2315c1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1326223616/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1326223616?pq-origsite=primo$$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/22815903$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Hotchin, Neil A.</contributor><creatorcontrib>deLeon, Orlando</creatorcontrib><creatorcontrib>Puglise, Jason M</creatorcontrib><creatorcontrib>Liu, Fengming</creatorcontrib><creatorcontrib>Smits, Jos</creatorcontrib><creatorcontrib>ter Beest, Martin B</creatorcontrib><creatorcontrib>Zegers, Mirjam M</creatorcontrib><title>Pak1 regulates the orientation of apical polarization and lumen formation by distinct pathways</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The development of the basic architecture of branching tubules enclosing a central lumen that characterizes most epithelial organs crucially depends on the apico-basolateral polarization of epithelial cells. Signals from the extracellular matrix control the orientation of the apical surface, so that it faces the lumen interior, opposite to cell-matrix adhesion sites. This orientation of the apical surface is thought to be intrinsically linked to the formation of single lumens. We previously demonstrated in three-dimensional cyst cultures of Madin-Darby canine kidney (MDCK) cells that signaling by β1 integrins regulates the orientation of the apical surface, via a mechanism that depends on the activity of the small GTPase Rac1. Here, we investigated whether the Rac1 effector Pak1 is a downstream effector in this pathway. Expression of constitutive active Pak1 phenocopies the effect of β1 integrin inhibition in that it misorients the apical surface and induces a multilumen phenotype. The misorientation of apical surfaces depends on the interaction of active Pak1 with PIX proteins and is linked to defects in basement membrane assembly. In contrast, the multilumen phenotype was independent of PIX and the basement membrane. Therefore, Pak1 likely regulates apical polarization and lumen formation by two distinct pathways.</description><subject>Animals</subject><subject>Biology</subject><subject>Biotinylation</subject><subject>Cancer</subject><subject>Cell adhesion & migration</subject><subject>Cell Line</subject><subject>Cell Polarity - physiology</subject><subject>Cell-Matrix Junctions</subject><subject>Cysts</subject><subject>Dogs</subject><subject>Drosophila</subject><subject>Epithelial cells</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - metabolism</subject><subject>Gene Expression Regulation</subject><subject>Genotype & phenotype</subject><subject>GTP Phosphohydrolases - metabolism</subject><subject>Guanosine triphosphatases</subject><subject>Guanosinetriphosphatase</subject><subject>Homeostasis</subject><subject>Immunoglobulins</subject><subject>Insects</subject><subject>Integrin beta1 - metabolism</subject><subject>Integrins</subject><subject>Kinases</subject><subject>Lumens</subject><subject>Microscopy, Confocal - 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Signals from the extracellular matrix control the orientation of the apical surface, so that it faces the lumen interior, opposite to cell-matrix adhesion sites. This orientation of the apical surface is thought to be intrinsically linked to the formation of single lumens. We previously demonstrated in three-dimensional cyst cultures of Madin-Darby canine kidney (MDCK) cells that signaling by β1 integrins regulates the orientation of the apical surface, via a mechanism that depends on the activity of the small GTPase Rac1. Here, we investigated whether the Rac1 effector Pak1 is a downstream effector in this pathway. Expression of constitutive active Pak1 phenocopies the effect of β1 integrin inhibition in that it misorients the apical surface and induces a multilumen phenotype. The misorientation of apical surfaces depends on the interaction of active Pak1 with PIX proteins and is linked to defects in basement membrane assembly. In contrast, the multilumen phenotype was independent of PIX and the basement membrane. Therefore, Pak1 likely regulates apical polarization and lumen formation by two distinct pathways.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22815903</pmid><doi>10.1371/journal.pone.0041039</doi><tpages>e41039</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biology Biotinylation Cancer Cell adhesion & migration Cell Line Cell Polarity - physiology Cell-Matrix Junctions Cysts Dogs Drosophila Epithelial cells Extracellular matrix Extracellular Matrix - metabolism Gene Expression Regulation Genotype & phenotype GTP Phosphohydrolases - metabolism Guanosine triphosphatases Guanosinetriphosphatase Homeostasis Immunoglobulins Insects Integrin beta1 - metabolism Integrins Kinases Lumens Microscopy, Confocal - methods Misalignment Models, Biological Morphogenesis Organs Orientation p21-Activated Kinases - metabolism Pathways Phenotype Phosphorylation Polarization Proteins Rac1 protein RNA, Small Interfering - metabolism Signaling Surgery Trypsin - chemistry Tubules |
title | Pak1 regulates the orientation of apical polarization and lumen formation by distinct pathways |
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