Iodide transporters expression in early human invasive trophoblast

Abstract Context The placenta plays an essential role in the fetomaternal exchanges of iodine and thyroid hormones. Propylthiouracil (PTU) is presently considered to be the treatment of choice for hyperthyroidism during the first trimester of pregnancy. Little is known on the expression of iodide tr...

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Veröffentlicht in:Placenta (Eastbourne) 2013-01, Vol.34 (1), p.29-34
Hauptverfasser: Degrelle, S.A, Guibourdenche, J, Galland, F, Bidart, J.M, Fournier, T, Evain-Brion, D
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container_end_page 34
container_issue 1
container_start_page 29
container_title Placenta (Eastbourne)
container_volume 34
creator Degrelle, S.A
Guibourdenche, J
Galland, F
Bidart, J.M
Fournier, T
Evain-Brion, D
description Abstract Context The placenta plays an essential role in the fetomaternal exchanges of iodine and thyroid hormones. Propylthiouracil (PTU) is presently considered to be the treatment of choice for hyperthyroidism during the first trimester of pregnancy. Little is known on the expression of iodide transporters in invasive human trophoblast and the possible effect of PTU on this early phase of human placental development. Objective To analyze during early pregnancy expression of sodium/iodide symporter (NIS) and pendrin at the feto–maternal interface in situ in first trimester placentas, in vitro during human trophoblastic cell differentiation in presence or not of PTU. Design NIS and pendrin immunodetection were performed on 8–10 WG placental tissue sections and in primary cultures of first trimester placenta trophoblastic cells, which differentiate in vitro into syncytiotrophoblast or invasive extravillous cytotrophoblasts (EVCT). The effect of PTU (1 mM) was tested in EVCT on iodide transporters expression, cell invasion, and hCG secretion. Results NIS and pendrin were present in early human trophoblast at the maternofetal interface. Their expression was modulated with in vitro trophoblast differentiation. Early invasive EVCT were characterized by higher expression of NIS than pendrin. In vitro PTU did modify significantly neither EVCT iodide transporters expression nor EVCT biological functions: i.e. invasive properties and hCG secretion. Conclusion This study reveals that NIS is highly expressed in early human trophoblast at the feto–maternal interface. PTU has no effect on early human trophoblast invasion.
doi_str_mv 10.1016/j.placenta.2012.11.002
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Propylthiouracil (PTU) is presently considered to be the treatment of choice for hyperthyroidism during the first trimester of pregnancy. Little is known on the expression of iodide transporters in invasive human trophoblast and the possible effect of PTU on this early phase of human placental development. Objective To analyze during early pregnancy expression of sodium/iodide symporter (NIS) and pendrin at the feto–maternal interface in situ in first trimester placentas, in vitro during human trophoblastic cell differentiation in presence or not of PTU. Design NIS and pendrin immunodetection were performed on 8–10 WG placental tissue sections and in primary cultures of first trimester placenta trophoblastic cells, which differentiate in vitro into syncytiotrophoblast or invasive extravillous cytotrophoblasts (EVCT). The effect of PTU (1 mM) was tested in EVCT on iodide transporters expression, cell invasion, and hCG secretion. Results NIS and pendrin were present in early human trophoblast at the maternofetal interface. Their expression was modulated with in vitro trophoblast differentiation. Early invasive EVCT were characterized by higher expression of NIS than pendrin. In vitro PTU did modify significantly neither EVCT iodide transporters expression nor EVCT biological functions: i.e. invasive properties and hCG secretion. Conclusion This study reveals that NIS is highly expressed in early human trophoblast at the feto–maternal interface. PTU has no effect on early human trophoblast invasion.</description><identifier>ISSN: 0143-4004</identifier><identifier>EISSN: 1532-3102</identifier><identifier>DOI: 10.1016/j.placenta.2012.11.002</identifier><identifier>PMID: 23174149</identifier><identifier>CODEN: PLACDF</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Antithyroid Agents - pharmacology ; Biological and medical sciences ; Cell Adhesion - drug effects ; Cell Adhesion - genetics ; Cell Differentiation - drug effects ; Cell Differentiation - genetics ; Cells, Cultured ; Drug Evaluation, Preclinical ; Embryology: invertebrates and vertebrates. Teratology ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Internal Medicine ; Iodine - metabolism ; Membrane Transport Proteins - genetics ; Membrane Transport Proteins - metabolism ; Models, Biological ; Obstetrics and Gynecology ; Pendrin ; Placenta ; Pregnancy ; Pregnancy Trimester, First - genetics ; Pregnancy Trimester, First - metabolism ; Primary Cell Culture ; Propylthiouracil ; Propylthiouracil - pharmacology ; Sodium/iodide symporter ; Symporters - genetics ; Symporters - metabolism ; Trophoblasts - drug effects ; Trophoblasts - metabolism ; Trophoblasts - physiology ; Villous and extravillous trophoblasts</subject><ispartof>Placenta (Eastbourne), 2013-01, Vol.34 (1), p.29-34</ispartof><rights>Elsevier Ltd</rights><rights>2012 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Ltd. 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Propylthiouracil (PTU) is presently considered to be the treatment of choice for hyperthyroidism during the first trimester of pregnancy. Little is known on the expression of iodide transporters in invasive human trophoblast and the possible effect of PTU on this early phase of human placental development. Objective To analyze during early pregnancy expression of sodium/iodide symporter (NIS) and pendrin at the feto–maternal interface in situ in first trimester placentas, in vitro during human trophoblastic cell differentiation in presence or not of PTU. Design NIS and pendrin immunodetection were performed on 8–10 WG placental tissue sections and in primary cultures of first trimester placenta trophoblastic cells, which differentiate in vitro into syncytiotrophoblast or invasive extravillous cytotrophoblasts (EVCT). The effect of PTU (1 mM) was tested in EVCT on iodide transporters expression, cell invasion, and hCG secretion. Results NIS and pendrin were present in early human trophoblast at the maternofetal interface. Their expression was modulated with in vitro trophoblast differentiation. Early invasive EVCT were characterized by higher expression of NIS than pendrin. In vitro PTU did modify significantly neither EVCT iodide transporters expression nor EVCT biological functions: i.e. invasive properties and hCG secretion. Conclusion This study reveals that NIS is highly expressed in early human trophoblast at the feto–maternal interface. PTU has no effect on early human trophoblast invasion.</description><subject>Antithyroid Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cell Adhesion - drug effects</subject><subject>Cell Adhesion - genetics</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Differentiation - genetics</subject><subject>Cells, Cultured</subject><subject>Drug Evaluation, Preclinical</subject><subject>Embryology: invertebrates and vertebrates. Teratology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Iodine - metabolism</subject><subject>Membrane Transport Proteins - genetics</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Models, Biological</subject><subject>Obstetrics and Gynecology</subject><subject>Pendrin</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, First - genetics</subject><subject>Pregnancy Trimester, First - metabolism</subject><subject>Primary Cell Culture</subject><subject>Propylthiouracil</subject><subject>Propylthiouracil - pharmacology</subject><subject>Sodium/iodide symporter</subject><subject>Symporters - genetics</subject><subject>Symporters - metabolism</subject><subject>Trophoblasts - drug effects</subject><subject>Trophoblasts - metabolism</subject><subject>Trophoblasts - physiology</subject><subject>Villous and extravillous trophoblasts</subject><issn>0143-4004</issn><issn>1532-3102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAQgC0EokvhL1S5IHFJ8NhOHF8QtOJRqRKHlrPlOBPVSzYOnmTF_nsSdgtSL73MaKRvHvqGsQvgBXCo3m-LsXceh8kVgoMoAArOxTO2gVKKXAIXz9mGg5K54lydsVdEW865USBesjMhQStQZsMur2MbWsym5AYaY5owUYa_x4REIQ5ZGDJ0qT9k9_POreXeUdivfBzvY9M7ml6zF53rCd-c8jn78eXz3dW3_Ob71-urTze5V6WccoPeoCqF002nWu-VqY2WWBrja-VL3bTQeN4o3YmyBSNFaWpd177RbQNSeHnO3h3njin-mpEmuwvkse_dgHEmC0JLUVW6qhe0OqI-RaKEnR1T2Ll0sMDt6s9u7YM_u_qzAHbxtzRenHbMzQ7bf20Pwhbg7Qlw5F3fLdp8oP9cpeuyFLBwH48cLkb2AZMlH3Dw2IaEfrJtDE_f8uHRCN-HISxbf-IBaRvnNCy-LVgSltvb9dvrs0H8DUL-ASleppQ</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Degrelle, S.A</creator><creator>Guibourdenche, J</creator><creator>Galland, F</creator><creator>Bidart, J.M</creator><creator>Fournier, T</creator><creator>Evain-Brion, D</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><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></search><sort><creationdate>20130101</creationdate><title>Iodide transporters expression in early human invasive trophoblast</title><author>Degrelle, S.A ; Guibourdenche, J ; Galland, F ; Bidart, J.M ; Fournier, T ; Evain-Brion, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-9ec9e452a7bf4dcc498973e599c84c57bd1bc0b47f25d1932598788cb7db132c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antithyroid Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Cell Adhesion - drug effects</topic><topic>Cell Adhesion - genetics</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Differentiation - genetics</topic><topic>Cells, Cultured</topic><topic>Drug Evaluation, Preclinical</topic><topic>Embryology: invertebrates and vertebrates. Teratology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Iodine - metabolism</topic><topic>Membrane Transport Proteins - genetics</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Models, Biological</topic><topic>Obstetrics and Gynecology</topic><topic>Pendrin</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First - genetics</topic><topic>Pregnancy Trimester, First - metabolism</topic><topic>Primary Cell Culture</topic><topic>Propylthiouracil</topic><topic>Propylthiouracil - pharmacology</topic><topic>Sodium/iodide symporter</topic><topic>Symporters - genetics</topic><topic>Symporters - metabolism</topic><topic>Trophoblasts - drug effects</topic><topic>Trophoblasts - metabolism</topic><topic>Trophoblasts - physiology</topic><topic>Villous and extravillous trophoblasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Degrelle, S.A</creatorcontrib><creatorcontrib>Guibourdenche, J</creatorcontrib><creatorcontrib>Galland, F</creatorcontrib><creatorcontrib>Bidart, J.M</creatorcontrib><creatorcontrib>Fournier, T</creatorcontrib><creatorcontrib>Evain-Brion, D</creatorcontrib><collection>Pascal-Francis</collection><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><jtitle>Placenta (Eastbourne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Degrelle, S.A</au><au>Guibourdenche, J</au><au>Galland, F</au><au>Bidart, J.M</au><au>Fournier, T</au><au>Evain-Brion, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iodide transporters expression in early human invasive trophoblast</atitle><jtitle>Placenta (Eastbourne)</jtitle><addtitle>Placenta</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>34</volume><issue>1</issue><spage>29</spage><epage>34</epage><pages>29-34</pages><issn>0143-4004</issn><eissn>1532-3102</eissn><coden>PLACDF</coden><abstract>Abstract Context The placenta plays an essential role in the fetomaternal exchanges of iodine and thyroid hormones. Propylthiouracil (PTU) is presently considered to be the treatment of choice for hyperthyroidism during the first trimester of pregnancy. Little is known on the expression of iodide transporters in invasive human trophoblast and the possible effect of PTU on this early phase of human placental development. Objective To analyze during early pregnancy expression of sodium/iodide symporter (NIS) and pendrin at the feto–maternal interface in situ in first trimester placentas, in vitro during human trophoblastic cell differentiation in presence or not of PTU. Design NIS and pendrin immunodetection were performed on 8–10 WG placental tissue sections and in primary cultures of first trimester placenta trophoblastic cells, which differentiate in vitro into syncytiotrophoblast or invasive extravillous cytotrophoblasts (EVCT). The effect of PTU (1 mM) was tested in EVCT on iodide transporters expression, cell invasion, and hCG secretion. Results NIS and pendrin were present in early human trophoblast at the maternofetal interface. Their expression was modulated with in vitro trophoblast differentiation. Early invasive EVCT were characterized by higher expression of NIS than pendrin. In vitro PTU did modify significantly neither EVCT iodide transporters expression nor EVCT biological functions: i.e. invasive properties and hCG secretion. Conclusion This study reveals that NIS is highly expressed in early human trophoblast at the feto–maternal interface. PTU has no effect on early human trophoblast invasion.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>23174149</pmid><doi>10.1016/j.placenta.2012.11.002</doi><tpages>6</tpages></addata></record>
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subjects Antithyroid Agents - pharmacology
Biological and medical sciences
Cell Adhesion - drug effects
Cell Adhesion - genetics
Cell Differentiation - drug effects
Cell Differentiation - genetics
Cells, Cultured
Drug Evaluation, Preclinical
Embryology: invertebrates and vertebrates. Teratology
Female
Fundamental and applied biological sciences. Psychology
Humans
Internal Medicine
Iodine - metabolism
Membrane Transport Proteins - genetics
Membrane Transport Proteins - metabolism
Models, Biological
Obstetrics and Gynecology
Pendrin
Placenta
Pregnancy
Pregnancy Trimester, First - genetics
Pregnancy Trimester, First - metabolism
Primary Cell Culture
Propylthiouracil
Propylthiouracil - pharmacology
Sodium/iodide symporter
Symporters - genetics
Symporters - metabolism
Trophoblasts - drug effects
Trophoblasts - metabolism
Trophoblasts - physiology
Villous and extravillous trophoblasts
title Iodide transporters expression in early human invasive trophoblast
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