Publication:
Basolateral Sorting of the Sodium/Iodide Symporter Is Mediated by Adaptor Protein 1 Clathrin Adaptor Complexes

dc.contributor.authorKoumarianou, Petrina
dc.contributor.authorFernández-Méndez, Celia
dc.contributor.authorFajardo-Delgado, Dánae
dc.contributor.authorMirela Mielu, Lidia
dc.contributor.authorSantisteban, Pilar
dc.contributor.authorDe la Vieja, Antonio
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderComunidad de Madrid (España)
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.contributor.funderCentro de Investigación Biomédica en Red - CIBERONC (Cáncer)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderAutonomous University of Madrid (España)
dc.date.accessioned2022-11-21T11:40:37Z
dc.date.available2022-11-21T11:40:37Z
dc.date.issued2022-10
dc.description.abstractBackground: The sodium/iodide symporter (NIS) is a transmembrane protein located on the basolateral membrane of thyrocytes. Despite its physiological and clinical relevance, little is known about the mechanisms that mediate NIS subcellular sorting. In the present study, we examined NIS basolateral trafficking in vitro using non-thyroid and thyroid epithelial cells. Methods: Immunofluorescence and Western blotting were performed to analyze NIS subcellular location and function in cells grown in monolayers under unpolarized and/or polarized conditions. Strategic NIS residues were mutated, and binding of NIS to clathrin adaptor complexes was determined by immunoprecipitation. Results: We show that NIS reaches the plasma membrane (PM) through a thyrotropin-dependent mechanism 24 hours after treatment with the hormone. We demonstrate that NIS basolateral trafficking is a clathrin-mediated mechanism, in which the clathrin adaptor complexes AP-1 (A and B) sort NIS from the trans-Golgi network (TGN) and recycling endosomes (REs). Specifically, we show that the AP-1B μ1 subunit controls NIS basolateral sorting through common REs. In its absence, NIS is apically missorted but remains functional. Additionally, direct NIS basolateral transport from the TGN to the basolateral membrane is mediated by AP-1A through clathrin-coated vesicles that also carry the transferrin receptor. Loss of the μ1 subunit of AP-1A is functionally compensated by AP-1B. Furthermore, loss of both subunits diminishes NIS trafficking to the PM. Finally, we demonstrate that AP-1A binds to the L121 and LL562/563 residues on NIS, whereas AP-1B binds to L583. Conclusions: Our findings highlight the novel involvement of the clathrin-coated machinery in basolateral NIS trafficking. Given that AP-1A expression is reduced in tumors, and its expression correlates with that of NIS, these findings will help uncover new targets in thyroid cancer treatment.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by grants PID2019-105303RB I00/AEI/10.13039/501100011033 from Ministerio de Ciencia e Innovación (MICIN) and B2017/BMD-3724, Tironet2-CM from Comunidad de Madrid (Spain) to P.S.; and SAF2015-69964-R, RTI2018-099343-B-100 from the MICIN, Spain, and Fondo Europeo de Desarrollo Regional to A.D.l.V. P.S. and A.D.l.V. laboratories are supported jointly by CIBERONC CB16/12/00326 from the Instituto de Salud Carlos III (ISCIII). P.K., C.F.-M., and L.M.M. held predoctoral fellowship from Ministerio de Economía y Competitividad, Universidad Autónoma de Madrid (Spain) and CIBERONC, respectively. D.F.-D. holds a contract associated with Grant SAF2015-69964-R.es_ES
dc.format.number10es_ES
dc.format.page1259-1270es_ES
dc.format.volume32es_ES
dc.identifier.citationThyroid. 2022 Oct;32(10):1259-1270.es_ES
dc.identifier.doi10.1089/thy.2022.0163es_ES
dc.identifier.e-issn1557-9077es_ES
dc.identifier.journalThyroid : official journal of the American Thyroid Associationes_ES
dc.identifier.pubmedID35833460es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/15208
dc.language.isoenges_ES
dc.publisherMary Ann Liebert
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/PID2019-105303RBI00/AEI/10.13039/501100011033es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/MINECO//SAF2015-69964-R/ES/MECANISMOS MOLECULARES DEL SIMPORTADOR NIS EN FISIOPATOLOGIA DE TIROIDES Y OVARIO/es_ES
dc.relation.projectFECYTinfo:eu-repo/grantAgreement/ES/RTI2018-099343-B-100es_ES
dc.relation.projectFISinfo:eu-repo/grantAgreement/ES/CB16/12/00326es_ES
dc.relation.publisherversionhttps://doi.org/10.1089/thy.2022.0163es_ES
dc.repisalud.centroISCIII::Unidad Funcional de Investigación de Enfermedades Crónicas (UFIEC)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectAP-1Aes_ES
dc.subjectAP-1Bes_ES
dc.subjectClathrines_ES
dc.subjectNIS traffickinges_ES
dc.subjectProtein sortinges_ES
dc.subjectSodium iodide symporteres_ES
dc.subject.meshIodideses_ES
dc.subject.meshSymporterses_ES
dc.subject.meshHumanses_ES
dc.subject.meshTranscription Factor AP-1es_ES
dc.subject.meshClathrines_ES
dc.subject.meshReceptors, Transferrines_ES
dc.subject.meshAdaptor Proteins, Vesicular Transportes_ES
dc.subject.meshThyrotropines_ES
dc.subject.meshHormoneses_ES
dc.subject.meshSodiumes_ES
dc.titleBasolateral Sorting of the Sodium/Iodide Symporter Is Mediated by Adaptor Protein 1 Clathrin Adaptor Complexeses_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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