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dc.contributor.authorZanardelli, Saraen
dc.contributor.authorChristodoulou, Neophytosen
dc.contributor.authorSkourides, Paris A.en
dc.creatorZanardelli, Saraen
dc.creatorChristodoulou, Neophytosen
dc.creatorSkourides, Paris A.en
dc.date.accessioned2019-11-04T12:52:54Z
dc.date.available2019-11-04T12:52:54Z
dc.date.issued2013
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/53457
dc.description.abstractCalpains are a family of calcium-dependent intracellular cysteine proteases that regulate several physiological processes by limited cleavage of different substrates. The role of Calpain2 in embryogenesis is not clear with conflicting evidence from a number of mouse knockouts. Here we report the temporal and spatial expression of Calpain2 in Xenopus laevis embryos and address its role in Xenopus development. We show that Calpain2 is expressed maternally with elevated expression in neural tissues and that Calpain2 activity is spatially and temporally regulated. Using a Calpain inhibitor, a dominant negative and a morpholino oligonoucleotide we demonstrate that impaired Calpain2 activity results in defective convergent extension both in mesodermal and neural tissues. Specifically, Calpain2 downregulation results in loss of tissue polarity and blockage of mediolateral intercalation in Keller explants without affecting adherens junction turnover. We further show that Calpain2 is activated in response to Wnt5a and that the inhibitory effect of Wnt5a expression on animal cap elongation can be rescued by blocking Calpain2 function. This suggests that Calpain2 activity needs to be tightly regulated during convergent extension. Finally we show that expression of Xdd1 blocks the membrane translocation of Calpain2 suggesting that Calpain2 activation is downstream of Dishevelled. Overall our data show that Calpain2 activation through the Wnt/Ca2+ pathway and Dishevelled can modulate convergent extension movements. © 2013 The Authors.en
dc.sourceDevelopmental biologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84886948196&doi=10.1016%2fj.ydbio.2013.09.017&partnerID=40&md5=dde52408765e6e99050ac93ab8e59983
dc.subjectarticleen
dc.subjectfemaleen
dc.subjectpriority journalen
dc.subjectprotein expressionen
dc.subjectdown regulationen
dc.subjectnonhumanen
dc.subjectanimal experimenten
dc.subjectanimal tissueen
dc.subjectenzyme activityen
dc.subjectAnimaliaen
dc.subjectembryoen
dc.subjectembryo developmenten
dc.subjectnervous tissueen
dc.subjectXenopusen
dc.subjectXenopus laevisen
dc.subjectcell polarityen
dc.subjectmesodermen
dc.subjectprotein transporten
dc.subjectConvergent extensionen
dc.subjectenzyme localizationen
dc.subjectenzyme regulationen
dc.subjectCalpainen
dc.subjectcalpain 2en
dc.subjectcalpastatinen
dc.subjectcell junctionen
dc.subjectdishevelled proteinen
dc.subjectexplanten
dc.subjectWnt5a proteinen
dc.titleCalpain2 protease: A new member of the Wnt/Ca2+ pathway modulating convergent extension movements in Xenopusen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.ydbio.2013.09.017
dc.description.volume384
dc.description.startingpage83
dc.description.endingpage100
dc.author.facultyΣχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Βιολογικών Επιστημών / Department of Biological Sciences
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :1</p>en
dc.source.abbreviationDev.Biol.en
dc.contributor.orcidSkourides, Paris A. [0000-0003-3502-5729]
dc.gnosis.orcid0000-0003-3502-5729


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