Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models

The polarized distribution of membrane proteins into apical and basolateral domains provides the basis for specialized functions of epithelial tissues. The EGF receptor (EGFR) plays important roles in embryonic development, adult-epithelial tissue homeostasis, and growth and survival of many carcino...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular biology of the cell 2023-11, Vol.34 (12), p.ar116-ar116
Hauptverfasser: Carlin, Cathleen R, Ngalula, Syntyche
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page ar116
container_issue 12
container_start_page ar116
container_title Molecular biology of the cell
container_volume 34
creator Carlin, Cathleen R
Ngalula, Syntyche
description The polarized distribution of membrane proteins into apical and basolateral domains provides the basis for specialized functions of epithelial tissues. The EGF receptor (EGFR) plays important roles in embryonic development, adult-epithelial tissue homeostasis, and growth and survival of many carcinomas. Typically targeted to basolateral domains, there is also considerable evidence of EGFR sorting plasticity but very limited knowledge regarding domain-specific EGFR substrates. Here we have investigated effects of selective EGFR mistargeting because of inactive-basolateral sorting signals on epithelial-cell homeostatic responses to growth-induced stress in MDCK cell models. Aberrant EGFR localization was associated with multilayer formation, anchorage-independent growth, and upregulated expression of the intermediate filament-protein vimentin characteristically seen in cells undergoing epithelial-to-mesenchymal transition. EGFRs were selectively retained following their internalization from apical membranes, and a signaling pathway involving the signaling adaptor Gab1 protein and extracellular signal-regulated kinase ERK5 had an essential role integrating multiple responses to growth-induced stress. Our studies highlight the potential importance of cellular machinery specifying EGFR polarity in epithelial pathologies associated with homeostatic imbalance.
doi_str_mv 10.1091/mbc.E23-04-0133
format Article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10846618</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A780289000</galeid><sourcerecordid>A780289000</sourcerecordid><originalsourceid>FETCH-LOGICAL-c420t-30c310620dabab25d3d892f1784c538359ba2d3f5034931438b7666b96945ec23</originalsourceid><addsrcrecordid>eNptkc9rFDEYhgdRbK2evUnAi5fZfvk5yUlK2VZhwYs9hyTzTTeSmYyTWaH_fbNsLRYkh4TkeV_y8TTNRwobCoZejj5stoy3IFqgnL9qzqnhphVSq9f1DNK0VDJx1rwr5RcAFUJ1b5sz3inRUSHPm7tdLoXkgWxvb8iCAec1L2TOyS1xfSA4OZ-wkH0eMZfVrTGQOHqX3BSQxIngHNc9puhSGzAlMuYeU3nfvBlcKvjhab9o7m62P6-_tbsft9-vr3ZtEAzWlkPgFBSD3nnnmex5rw0baKdFkFxzabxjPR8kcGE4FVz7TinljTJCYmD8ovl66p0PfsQ-4LQuLtl5iaNbHmx20b58meLe3uc_loIWSlFdG748NSz59wHLasdYjpO4CfOhWKalUcBN11X08wm9dwltnIZcK8MRt1edBqYNAFRq8x-qrh7HGPKEQ6z3LwKXp0BYqooFh-fvU7BHybZKtlWyBWGPkmvi079TP_N_rfJHAZmhmQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2859603977</pqid></control><display><type>article</type><title>Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models</title><source>MEDLINE</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Carlin, Cathleen R ; Ngalula, Syntyche</creator><contributor>Sorkin, Alexander</contributor><creatorcontrib>Carlin, Cathleen R ; Ngalula, Syntyche ; Sorkin, Alexander</creatorcontrib><description>The polarized distribution of membrane proteins into apical and basolateral domains provides the basis for specialized functions of epithelial tissues. The EGF receptor (EGFR) plays important roles in embryonic development, adult-epithelial tissue homeostasis, and growth and survival of many carcinomas. Typically targeted to basolateral domains, there is also considerable evidence of EGFR sorting plasticity but very limited knowledge regarding domain-specific EGFR substrates. Here we have investigated effects of selective EGFR mistargeting because of inactive-basolateral sorting signals on epithelial-cell homeostatic responses to growth-induced stress in MDCK cell models. Aberrant EGFR localization was associated with multilayer formation, anchorage-independent growth, and upregulated expression of the intermediate filament-protein vimentin characteristically seen in cells undergoing epithelial-to-mesenchymal transition. EGFRs were selectively retained following their internalization from apical membranes, and a signaling pathway involving the signaling adaptor Gab1 protein and extracellular signal-regulated kinase ERK5 had an essential role integrating multiple responses to growth-induced stress. Our studies highlight the potential importance of cellular machinery specifying EGFR polarity in epithelial pathologies associated with homeostatic imbalance.</description><identifier>ISSN: 1059-1524</identifier><identifier>EISSN: 1939-4586</identifier><identifier>DOI: 10.1091/mbc.E23-04-0133</identifier><identifier>PMID: 37647145</identifier><language>eng</language><publisher>United States: American Society for Cell Biology</publisher><subject>Animals ; Cell Membrane - metabolism ; Cell Polarity - physiology ; Dogs ; Epithelial cells ; Epithelial Cells - metabolism ; ErbB Receptors - metabolism ; Health aspects ; Homeostasis ; Madin Darby Canine Kidney Cells ; Membrane Proteins - metabolism ; Polarity (Biology)</subject><ispartof>Molecular biology of the cell, 2023-11, Vol.34 (12), p.ar116-ar116</ispartof><rights>COPYRIGHT 2023 American Society for Cell Biology</rights><rights>2023 Carlin and Ngalula. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-30c310620dabab25d3d892f1784c538359ba2d3f5034931438b7666b96945ec23</citedby><cites>FETCH-LOGICAL-c420t-30c310620dabab25d3d892f1784c538359ba2d3f5034931438b7666b96945ec23</cites><orcidid>0000-0002-3569-4247</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10846618/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10846618/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37647145$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Sorkin, Alexander</contributor><creatorcontrib>Carlin, Cathleen R</creatorcontrib><creatorcontrib>Ngalula, Syntyche</creatorcontrib><title>Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models</title><title>Molecular biology of the cell</title><addtitle>Mol Biol Cell</addtitle><description>The polarized distribution of membrane proteins into apical and basolateral domains provides the basis for specialized functions of epithelial tissues. The EGF receptor (EGFR) plays important roles in embryonic development, adult-epithelial tissue homeostasis, and growth and survival of many carcinomas. Typically targeted to basolateral domains, there is also considerable evidence of EGFR sorting plasticity but very limited knowledge regarding domain-specific EGFR substrates. Here we have investigated effects of selective EGFR mistargeting because of inactive-basolateral sorting signals on epithelial-cell homeostatic responses to growth-induced stress in MDCK cell models. Aberrant EGFR localization was associated with multilayer formation, anchorage-independent growth, and upregulated expression of the intermediate filament-protein vimentin characteristically seen in cells undergoing epithelial-to-mesenchymal transition. EGFRs were selectively retained following their internalization from apical membranes, and a signaling pathway involving the signaling adaptor Gab1 protein and extracellular signal-regulated kinase ERK5 had an essential role integrating multiple responses to growth-induced stress. Our studies highlight the potential importance of cellular machinery specifying EGFR polarity in epithelial pathologies associated with homeostatic imbalance.</description><subject>Animals</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Polarity - physiology</subject><subject>Dogs</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - metabolism</subject><subject>ErbB Receptors - metabolism</subject><subject>Health aspects</subject><subject>Homeostasis</subject><subject>Madin Darby Canine Kidney Cells</subject><subject>Membrane Proteins - metabolism</subject><subject>Polarity (Biology)</subject><issn>1059-1524</issn><issn>1939-4586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkc9rFDEYhgdRbK2evUnAi5fZfvk5yUlK2VZhwYs9hyTzTTeSmYyTWaH_fbNsLRYkh4TkeV_y8TTNRwobCoZejj5stoy3IFqgnL9qzqnhphVSq9f1DNK0VDJx1rwr5RcAFUJ1b5sz3inRUSHPm7tdLoXkgWxvb8iCAec1L2TOyS1xfSA4OZ-wkH0eMZfVrTGQOHqX3BSQxIngHNc9puhSGzAlMuYeU3nfvBlcKvjhab9o7m62P6-_tbsft9-vr3ZtEAzWlkPgFBSD3nnnmex5rw0baKdFkFxzabxjPR8kcGE4FVz7TinljTJCYmD8ovl66p0PfsQ-4LQuLtl5iaNbHmx20b58meLe3uc_loIWSlFdG748NSz59wHLasdYjpO4CfOhWKalUcBN11X08wm9dwltnIZcK8MRt1edBqYNAFRq8x-qrh7HGPKEQ6z3LwKXp0BYqooFh-fvU7BHybZKtlWyBWGPkmvi079TP_N_rfJHAZmhmQ</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Carlin, Cathleen R</creator><creator>Ngalula, Syntyche</creator><general>American Society for Cell Biology</general><general>The American Society for Cell Biology</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>5PM</scope><orcidid>https://orcid.org/0000-0002-3569-4247</orcidid></search><sort><creationdate>20231101</creationdate><title>Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models</title><author>Carlin, Cathleen R ; Ngalula, Syntyche</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-30c310620dabab25d3d892f1784c538359ba2d3f5034931438b7666b96945ec23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Polarity - physiology</topic><topic>Dogs</topic><topic>Epithelial cells</topic><topic>Epithelial Cells - metabolism</topic><topic>ErbB Receptors - metabolism</topic><topic>Health aspects</topic><topic>Homeostasis</topic><topic>Madin Darby Canine Kidney Cells</topic><topic>Membrane Proteins - metabolism</topic><topic>Polarity (Biology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carlin, Cathleen R</creatorcontrib><creatorcontrib>Ngalula, Syntyche</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>PubMed Central (Full Participant titles)</collection><jtitle>Molecular biology of the cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carlin, Cathleen R</au><au>Ngalula, Syntyche</au><au>Sorkin, Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models</atitle><jtitle>Molecular biology of the cell</jtitle><addtitle>Mol Biol Cell</addtitle><date>2023-11-01</date><risdate>2023</risdate><volume>34</volume><issue>12</issue><spage>ar116</spage><epage>ar116</epage><pages>ar116-ar116</pages><issn>1059-1524</issn><eissn>1939-4586</eissn><abstract>The polarized distribution of membrane proteins into apical and basolateral domains provides the basis for specialized functions of epithelial tissues. The EGF receptor (EGFR) plays important roles in embryonic development, adult-epithelial tissue homeostasis, and growth and survival of many carcinomas. Typically targeted to basolateral domains, there is also considerable evidence of EGFR sorting plasticity but very limited knowledge regarding domain-specific EGFR substrates. Here we have investigated effects of selective EGFR mistargeting because of inactive-basolateral sorting signals on epithelial-cell homeostatic responses to growth-induced stress in MDCK cell models. Aberrant EGFR localization was associated with multilayer formation, anchorage-independent growth, and upregulated expression of the intermediate filament-protein vimentin characteristically seen in cells undergoing epithelial-to-mesenchymal transition. EGFRs were selectively retained following their internalization from apical membranes, and a signaling pathway involving the signaling adaptor Gab1 protein and extracellular signal-regulated kinase ERK5 had an essential role integrating multiple responses to growth-induced stress. Our studies highlight the potential importance of cellular machinery specifying EGFR polarity in epithelial pathologies associated with homeostatic imbalance.</abstract><cop>United States</cop><pub>American Society for Cell Biology</pub><pmid>37647145</pmid><doi>10.1091/mbc.E23-04-0133</doi><orcidid>https://orcid.org/0000-0002-3569-4247</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1059-1524
ispartof Molecular biology of the cell, 2023-11, Vol.34 (12), p.ar116-ar116
issn 1059-1524
1939-4586
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10846618
source MEDLINE; PubMed Central; Free Full-Text Journals in Chemistry
subjects Animals
Cell Membrane - metabolism
Cell Polarity - physiology
Dogs
Epithelial cells
Epithelial Cells - metabolism
ErbB Receptors - metabolism
Health aspects
Homeostasis
Madin Darby Canine Kidney Cells
Membrane Proteins - metabolism
Polarity (Biology)
title Loss of EGF receptor polarity enables homeostatic imbalance in epithelial-cell models
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T19%3A49%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Loss%20of%20EGF%20receptor%20polarity%20enables%20homeostatic%20imbalance%20in%20epithelial-cell%20models&rft.jtitle=Molecular%20biology%20of%20the%20cell&rft.au=Carlin,%20Cathleen%20R&rft.date=2023-11-01&rft.volume=34&rft.issue=12&rft.spage=ar116&rft.epage=ar116&rft.pages=ar116-ar116&rft.issn=1059-1524&rft.eissn=1939-4586&rft_id=info:doi/10.1091/mbc.E23-04-0133&rft_dat=%3Cgale_pubme%3EA780289000%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2859603977&rft_id=info:pmid/37647145&rft_galeid=A780289000&rfr_iscdi=true