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dc.contributor.authorPistritto, Giuseppa
dc.contributor.authorPapaleo, Veruska
dc.contributor.authorSánchez Medina, María Pilar 
dc.contributor.authorCeci, Claudia
dc.contributor.authorBarbaccia, Maria Luisa
dc.date.accessioned2014-03-18T11:35:12Z
dc.date.available2014-03-18T11:35:12Z
dc.date.issued2012
dc.identifier.citationPistritto, G.; et al. Divergent Modulation of Neuronal Differentiation by Caspase-2 and -9. Plos One, 7(5): e36002 (2012). [http://hdl.handle.net/10481/30926]es_ES
dc.identifier.issn1932-6203
dc.identifier.otherdoi: 10.1371/journal.pone.0036002
dc.identifier.urihttp://hdl.handle.net/10481/30926
dc.description.abstractHuman Ntera2/cl.D1 (NT2) cells treated with retinoic acid (RA) differentiate towards a well characterized neuronal phenotype sharing many features with human fetal neurons. In view of the emerging role of caspases in murine stem cell/neural precursor differentiation, caspases activity was evaluated during RA differentiation. Caspase-2, -3 and -9 activity was transiently and selectively increased in differentiating and non-apoptotic NT2-cells. SiRNA-mediated selective silencing of either caspase-2 (si-Casp2) or -9 (si-Casp9) was implemented in order to dissect the role of distinct caspases. The RA-induced expression of neuronal markers, i.e. neural cell adhesion molecule (NCAM), microtubule associated protein-2 (MAP2) and tyrosine hydroxylase (TH) mRNAs and proteins, was decreased in si-Casp9, but markedly increased in si-Casp2 cells. During RA-induced NT2 differentiation, the class III histone deacetylase Sirt1, a putative caspase substrate implicated in the regulation of the proneural bHLH MASH1 gene expression, was cleaved to a ~100 kDa fragment. Sirt1 cleavage was markedly reduced in si-Casp9 cells, even though caspase-3 was normally activated, but was not affected (still cleaved) in si-Casp2 cells, despite a marked reduction of caspase-3 activity. The expression of MASH1 mRNA was higher and occurred earlier in si-Casp2 cells, while was reduced at early time points during differentiation in si-Casp9 cells. Thus, caspase-2 and -9 may perform opposite functions during RA-induced NT2 neuronal differentiation. While caspase-9 activation is relevant for proper neuronal differentiation, likely through the fine tuning of Sirt1 function, caspase-2 activation appears to hinder the RA-induced neuronal differentiation of NT2 cells.es_ES
dc.description.sponsorshipThis work was partially supported by a grant (n. 212413102008) from Regione Calabria-Italy and from the Research Fund of Tor Vergata University, Rome, Italy.es_ES
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS)es_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.subjectAdhesion moleculeses_ES
dc.subjectApoptosises_ES
dc.subjectCell differentiationes_ES
dc.subjectHistones es_ES
dc.subjectNeuronal differentiationes_ES
dc.subjectNeurons es_ES
dc.subjectOrganism developmentes_ES
dc.subjectProtein expressiones_ES
dc.titleDivergent Modulation of Neuronal Differentiation by Caspase-2 and -9es_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES


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