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dc.contributor.authorMuguruza Montero, Arantza
dc.contributor.authorNuñez, Eider
dc.contributor.authorAraujo, Ariane
dc.contributor.authorAlicante, Sara
dc.contributor.authorVillarroel, Alvaro
dc.contributor.authorUrrutia Iñiguez, Janire
dc.date.accessioned2022-09-08T10:05:51Z
dc.date.available2022-09-08T10:05:51Z
dc.date.issued2022
dc.identifier.citationEkaia 42 : 173-191 (2022)
dc.identifier.issn0214-9001
dc.identifier.urihttp://hdl.handle.net/10810/57535
dc.description.abstractCalcium is a universal signaling messenger that participates in essential processes such as apoptosis, cell proliferation and muscle contraction. Many of the proteins involved in these processes must interact with a calcium sensor to respond to the changes of concentration of this ion. The best-studied sensor is Calmodulin (CaM). It regulates the activity of hundreds of proteins through its N- and C- lobes, where two EF-hands are located to bind up to four calcium ions. Although the role of CaM in cell signaling is widespread, its mutations are especially recognized through its effects on cardiac function. In fact, disease-causing mutations in any of the three genes that encode the same CaM proteins cause severe cardiac dysfunction, indicating their importance in regulating excitability. Therefore, knowing the mechanisms involved in these diseases can allow a rational approach to clinical manifestations and contribute to the development of therapeutic strategies.; Kaltzioa seinalizazio unibertsaleko mezulari bat da, funtsezko prozesuetan parte hartzen duena, hala nola apoptosian, zelulen proliferazioan eta muskuluen uzkurduran. Prozesu horietan parte hartzen duten proteina askok ioi honen kontzentrazioari erantzuteko kaltzio sentsore batekin, kalmodulinarekin (CaM), elkarreragin behar dute. Horrek ehunka proteinaren aktibitatea erregulatzen du bere N- eta C-lobuluen bidez, non EF-eskuak aurkezten dituen Ca2+-ari lotzeko. Zelulen seinalizazioan CaM-k duen papera hedatuta dagoen arren, haren mutazioek bereziki bihotzari eragiten diote. Izan ere, CaM proteina berdinak kodetzen dituzten hiru geneetako edozeinetan gaixotasunak eragiten dituzten mutazioek bihotz-disfuntzio larriak eragiten dituzte, eta horrek kitzikagarritasunaren erregulazioan duen garrantzia adierazten du. Beraz, esku hartzen duten mekanismoen ezagutzak aukera eman dezake adierazpen klinikoei modu kritikoan heltzeko eta kalmodulinopatietarako estrategia terapeutikoak garatzen laguntzeko.
dc.language.isoeus
dc.publisherServicio Editorial de la Universidad del País Vasco/Euskal Herriko Unibertsitatearen Argitalpen Zerbitzua
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.titleGure bihotzeko kalmodulina
dc.typeinfo:eu-repo/semantics/article
dc.rights.holder© 2022 UPV/EHU Attribution-NonCommercial-ShareAlike 4.0 International
dc.identifier.doi10.1387/ekaia.22935


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© 2022 UPV/EHU Attribution-NonCommercial-ShareAlike 4.0 International
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