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Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells
This study compared the effects of benzo( a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo- p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to 10 μ M BaP significantly decreased cell attachmen...
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Published in: | Biochemical and biophysical research communications 2002-05, Vol.294 (1), p.101-107 |
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creator | McGarry, Michelle A Charles, Grantley D Medrano, Theresa Bubb, Michael R Grant, Maria B Campbell-Thompson, Martha Shiverick, Kathleen T |
description | This study compared the effects of benzo(
a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to
10
μ
M BaP significantly decreased cell attachment to Matrigel, whereas 10
nM TCDD had no effect. Immunocytochemistry and Western immunoblot analysis showed that BaP, but not TCDD, produced a marked loss of plasma membrane epidermal growth factor receptor (EGF-R) localized along intercellular boundaries. BaP-treated cells exhibited significant decreases in β-catenin and cadherin protein levels, while vinculin levels remained unchanged relative to control. In contrast, TCDD treatment had no effect on the levels of β-catenin, cadherin, or vinculin. Further studies using the fluorescein labeled peptide phalloidin showed the presence of continuous subcortical actin filaments in control cells, whereas BaP-treated cells had subcortical actin aggregates. Thus, in contrast to TCDD, BaP produces a loss of cell attachment involving decreased localization of molecules important for cell–cell interactions in RL95-2 cells. |
doi_str_mv | 10.1016/S0006-291X(02)00437-0 |
format | article |
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a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to
10
μ
M BaP significantly decreased cell attachment to Matrigel, whereas 10
nM TCDD had no effect. Immunocytochemistry and Western immunoblot analysis showed that BaP, but not TCDD, produced a marked loss of plasma membrane epidermal growth factor receptor (EGF-R) localized along intercellular boundaries. BaP-treated cells exhibited significant decreases in β-catenin and cadherin protein levels, while vinculin levels remained unchanged relative to control. In contrast, TCDD treatment had no effect on the levels of β-catenin, cadherin, or vinculin. Further studies using the fluorescein labeled peptide phalloidin showed the presence of continuous subcortical actin filaments in control cells, whereas BaP-treated cells had subcortical actin aggregates. Thus, in contrast to TCDD, BaP produces a loss of cell attachment involving decreased localization of molecules important for cell–cell interactions in RL95-2 cells.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/S0006-291X(02)00437-0</identifier><identifier>PMID: 12054747</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Actins - drug effects ; Actins - metabolism ; Adhesion ; Attachment ; BaP ; Benzo(a)pyrene - pharmacology ; beta Catenin ; Blotting, Western ; Cadherin ; Cadherins - metabolism ; Cell Adhesion - drug effects ; Cell Adhesion Molecules - drug effects ; Cell Adhesion Molecules - metabolism ; Cell Line ; Cell Membrane - drug effects ; Cell Membrane - metabolism ; Cytoskeletal Proteins - metabolism ; Cytoskeleton ; Dimethyl Sulfoxide - pharmacology ; EGF-R ; Endometrium - drug effects ; Endometrium - metabolism ; Female ; Human uterine endometrium ; Humans ; Phalloidine - metabolism ; Polychlorinated Dibenzodioxins - pharmacology ; Receptor, Epidermal Growth Factor - metabolism ; Receptors, Aryl Hydrocarbon - agonists ; TCDD ; Trans-Activators ; Uterus - drug effects ; Uterus - metabolism ; Vinculin - metabolism ; β-catenin</subject><ispartof>Biochemical and biophysical research communications, 2002-05, Vol.294 (1), p.101-107</ispartof><rights>2002 Elsevier Science (USA)</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-b75d7dd29a1c6f649fe4583fdb818246977017eaeca70ae05ee04b120e86e66a3</citedby><cites>FETCH-LOGICAL-c392t-b75d7dd29a1c6f649fe4583fdb818246977017eaeca70ae05ee04b120e86e66a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12054747$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McGarry, Michelle A</creatorcontrib><creatorcontrib>Charles, Grantley D</creatorcontrib><creatorcontrib>Medrano, Theresa</creatorcontrib><creatorcontrib>Bubb, Michael R</creatorcontrib><creatorcontrib>Grant, Maria B</creatorcontrib><creatorcontrib>Campbell-Thompson, Martha</creatorcontrib><creatorcontrib>Shiverick, Kathleen T</creatorcontrib><title>Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>This study compared the effects of benzo(
a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to
10
μ
M BaP significantly decreased cell attachment to Matrigel, whereas 10
nM TCDD had no effect. Immunocytochemistry and Western immunoblot analysis showed that BaP, but not TCDD, produced a marked loss of plasma membrane epidermal growth factor receptor (EGF-R) localized along intercellular boundaries. BaP-treated cells exhibited significant decreases in β-catenin and cadherin protein levels, while vinculin levels remained unchanged relative to control. In contrast, TCDD treatment had no effect on the levels of β-catenin, cadherin, or vinculin. Further studies using the fluorescein labeled peptide phalloidin showed the presence of continuous subcortical actin filaments in control cells, whereas BaP-treated cells had subcortical actin aggregates. Thus, in contrast to TCDD, BaP produces a loss of cell attachment involving decreased localization of molecules important for cell–cell interactions in RL95-2 cells.</description><subject>Actins - drug effects</subject><subject>Actins - metabolism</subject><subject>Adhesion</subject><subject>Attachment</subject><subject>BaP</subject><subject>Benzo(a)pyrene - pharmacology</subject><subject>beta Catenin</subject><subject>Blotting, Western</subject><subject>Cadherin</subject><subject>Cadherins - metabolism</subject><subject>Cell Adhesion - drug effects</subject><subject>Cell Adhesion Molecules - drug effects</subject><subject>Cell Adhesion Molecules - metabolism</subject><subject>Cell Line</subject><subject>Cell Membrane - drug effects</subject><subject>Cell Membrane - metabolism</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>Cytoskeleton</subject><subject>Dimethyl Sulfoxide - pharmacology</subject><subject>EGF-R</subject><subject>Endometrium - drug effects</subject><subject>Endometrium - metabolism</subject><subject>Female</subject><subject>Human uterine endometrium</subject><subject>Humans</subject><subject>Phalloidine - metabolism</subject><subject>Polychlorinated Dibenzodioxins - pharmacology</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Receptors, Aryl Hydrocarbon - agonists</subject><subject>TCDD</subject><subject>Trans-Activators</subject><subject>Uterus - drug effects</subject><subject>Uterus - metabolism</subject><subject>Vinculin - metabolism</subject><subject>β-catenin</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkF1rFTEQhoNY2mPtT1ByJS1s6iT7kd0rsUVt4UChKngXssksJ7InOSZZafvru-cDe-nV3Dwz77wPIe84XHLgzcfvANAw0fFf5yAuAKpSMnhFFhw6YIJD9Zos_iEn5E1KvwE4r5rumJxwAXUlK7kgT1fon8I51Rebx4geC9pPmfqQqSjKQhYty5ijNqsxxGBdv6UZ3TDrwoPzBdVjxpiowXGk2q4wueDpJoaMzifqPF1Na-3pNFPOI71fdjUTOzy9JUeDHhOeHeYp-fn1y4_rG7a8-3Z7_XnJTNmJzHpZW2mt6DQ3zdBU3YBV3ZaD7VveirmPlMAlajRagkaoEaHq54bYNtg0ujwlH_Z357f-TJiyWru0_UB7DFNSvGtByFbMYL0HTQwpRRzUJrq1jo-Kg9pKVzvpamtUgVA76QrmvfeHgKlfo33ZOliegU97AOeafx1GlYxDb9C6iCYrG9x_Ip4B_seQvQ</recordid><startdate>20020531</startdate><enddate>20020531</enddate><creator>McGarry, Michelle A</creator><creator>Charles, Grantley D</creator><creator>Medrano, Theresa</creator><creator>Bubb, Michael R</creator><creator>Grant, Maria B</creator><creator>Campbell-Thompson, Martha</creator><creator>Shiverick, Kathleen T</creator><general>Elsevier Inc</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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20020531</creationdate><title>Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells</title><author>McGarry, Michelle A ; Charles, Grantley D ; Medrano, Theresa ; Bubb, Michael R ; Grant, Maria B ; Campbell-Thompson, Martha ; Shiverick, Kathleen T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-b75d7dd29a1c6f649fe4583fdb818246977017eaeca70ae05ee04b120e86e66a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Actins - drug effects</topic><topic>Actins - metabolism</topic><topic>Adhesion</topic><topic>Attachment</topic><topic>BaP</topic><topic>Benzo(a)pyrene - pharmacology</topic><topic>beta Catenin</topic><topic>Blotting, Western</topic><topic>Cadherin</topic><topic>Cadherins - metabolism</topic><topic>Cell Adhesion - drug effects</topic><topic>Cell Adhesion Molecules - drug effects</topic><topic>Cell Adhesion Molecules - metabolism</topic><topic>Cell Line</topic><topic>Cell Membrane - drug effects</topic><topic>Cell Membrane - metabolism</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>Cytoskeleton</topic><topic>Dimethyl Sulfoxide - pharmacology</topic><topic>EGF-R</topic><topic>Endometrium - drug effects</topic><topic>Endometrium - metabolism</topic><topic>Female</topic><topic>Human uterine endometrium</topic><topic>Humans</topic><topic>Phalloidine - metabolism</topic><topic>Polychlorinated Dibenzodioxins - pharmacology</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Receptors, Aryl Hydrocarbon - agonists</topic><topic>TCDD</topic><topic>Trans-Activators</topic><topic>Uterus - drug effects</topic><topic>Uterus - metabolism</topic><topic>Vinculin - metabolism</topic><topic>β-catenin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McGarry, Michelle A</creatorcontrib><creatorcontrib>Charles, Grantley D</creatorcontrib><creatorcontrib>Medrano, Theresa</creatorcontrib><creatorcontrib>Bubb, Michael R</creatorcontrib><creatorcontrib>Grant, Maria B</creatorcontrib><creatorcontrib>Campbell-Thompson, Martha</creatorcontrib><creatorcontrib>Shiverick, Kathleen T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McGarry, Michelle A</au><au>Charles, Grantley D</au><au>Medrano, Theresa</au><au>Bubb, Michael R</au><au>Grant, Maria B</au><au>Campbell-Thompson, Martha</au><au>Shiverick, Kathleen T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2002-05-31</date><risdate>2002</risdate><volume>294</volume><issue>1</issue><spage>101</spage><epage>107</epage><pages>101-107</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>This study compared the effects of benzo(
a)pyrene (BaP) and 2,3,7,8-tetrachlorodibenzo-
p-dioxin (TCDD), two aryl hydrocarbon receptor agonists, on cell attachment and adherens junction proteins in RL95-2 human uterine endometrial cells. Exposure to
10
μ
M BaP significantly decreased cell attachment to Matrigel, whereas 10
nM TCDD had no effect. Immunocytochemistry and Western immunoblot analysis showed that BaP, but not TCDD, produced a marked loss of plasma membrane epidermal growth factor receptor (EGF-R) localized along intercellular boundaries. BaP-treated cells exhibited significant decreases in β-catenin and cadherin protein levels, while vinculin levels remained unchanged relative to control. In contrast, TCDD treatment had no effect on the levels of β-catenin, cadherin, or vinculin. Further studies using the fluorescein labeled peptide phalloidin showed the presence of continuous subcortical actin filaments in control cells, whereas BaP-treated cells had subcortical actin aggregates. Thus, in contrast to TCDD, BaP produces a loss of cell attachment involving decreased localization of molecules important for cell–cell interactions in RL95-2 cells.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12054747</pmid><doi>10.1016/S0006-291X(02)00437-0</doi><tpages>7</tpages></addata></record> |
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subjects | Actins - drug effects Actins - metabolism Adhesion Attachment BaP Benzo(a)pyrene - pharmacology beta Catenin Blotting, Western Cadherin Cadherins - metabolism Cell Adhesion - drug effects Cell Adhesion Molecules - drug effects Cell Adhesion Molecules - metabolism Cell Line Cell Membrane - drug effects Cell Membrane - metabolism Cytoskeletal Proteins - metabolism Cytoskeleton Dimethyl Sulfoxide - pharmacology EGF-R Endometrium - drug effects Endometrium - metabolism Female Human uterine endometrium Humans Phalloidine - metabolism Polychlorinated Dibenzodioxins - pharmacology Receptor, Epidermal Growth Factor - metabolism Receptors, Aryl Hydrocarbon - agonists TCDD Trans-Activators Uterus - drug effects Uterus - metabolism Vinculin - metabolism β-catenin |
title | Benzo( a)pyrene, but not 2,3,7,8-tetrachlorodibenzo- p-dioxin, alters cell adhesion proteins in human uterine RL95-2 cells |
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