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Article: p73: A multifunctional protein in neurobiology

Titlep73: A multifunctional protein in neurobiology
Authors
KeywordsNeural stem cells (NSC)
Neurodegeneration
P73
Neuronal differentiation
Alzheimer's disease
Issue Date2011
Citation
Molecular Neurobiology, 2011, v. 43, n. 2, p. 139-146 How to Cite?
AbstractP73, a transcription factor of the p53 family, plays a key role in many biological processes including neuronal development. Indeed, mice deficient for both TAp73 and ΔNp73 isoforms display neuronal pathologies, including hydrocephalus and hippocampal dysgenesis, with defects in the CA1-CA3 pyramidal cell layers and the dentate gyrus. TAp73 expression increases in parallel with neuronal differentiation and its ectopic expression induces neurite outgrowth and expression of neuronal markers in neuroblastoma cell lines and neural stem cells, suggesting that it has a pro-differentiation role. In contrast, ΔNp73 shows a survival function in mature cortical neurons as selective ΔNp73 null mice have reduced cortical thickness. Recent evidence has also suggested that p73 isoforms are deregulated in neurodegenerative pathologies such as Alzheimer's disease, with abnormal tau phosphorylation. Thus, in addition to its increasingly accepted contribution to tumorigenesis, the p73 subfamily also plays a role in neuronal development and neurodegeneration.
Persistent Identifierhttp://hdl.handle.net/10722/292639
ISSN
2021 Impact Factor: 5.682
2020 SCImago Journal Rankings: 1.569
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKillick, Richard-
dc.contributor.authorNiklison-Chirou, Maria-
dc.contributor.authorTomasini, Richard-
dc.contributor.authorBano, Daniele-
dc.contributor.authorRufini, Alessandro-
dc.contributor.authorGrespi, Francesca-
dc.contributor.authorVelletri, Tania-
dc.contributor.authorTucci, Paola-
dc.contributor.authorSayan, Berna S.-
dc.contributor.authorConforti, Franco-
dc.contributor.authorGallagher, Ewen-
dc.contributor.authorNicotera, Pierluigi-
dc.contributor.authorMak, Tak W.-
dc.contributor.authorMelino, Gerry-
dc.contributor.authorKnight, Richard A.-
dc.contributor.authorAgostini, Massimiliano-
dc.date.accessioned2020-11-17T14:56:54Z-
dc.date.available2020-11-17T14:56:54Z-
dc.date.issued2011-
dc.identifier.citationMolecular Neurobiology, 2011, v. 43, n. 2, p. 139-146-
dc.identifier.issn0893-7648-
dc.identifier.urihttp://hdl.handle.net/10722/292639-
dc.description.abstractP73, a transcription factor of the p53 family, plays a key role in many biological processes including neuronal development. Indeed, mice deficient for both TAp73 and ΔNp73 isoforms display neuronal pathologies, including hydrocephalus and hippocampal dysgenesis, with defects in the CA1-CA3 pyramidal cell layers and the dentate gyrus. TAp73 expression increases in parallel with neuronal differentiation and its ectopic expression induces neurite outgrowth and expression of neuronal markers in neuroblastoma cell lines and neural stem cells, suggesting that it has a pro-differentiation role. In contrast, ΔNp73 shows a survival function in mature cortical neurons as selective ΔNp73 null mice have reduced cortical thickness. Recent evidence has also suggested that p73 isoforms are deregulated in neurodegenerative pathologies such as Alzheimer's disease, with abnormal tau phosphorylation. Thus, in addition to its increasingly accepted contribution to tumorigenesis, the p73 subfamily also plays a role in neuronal development and neurodegeneration.-
dc.languageeng-
dc.relation.ispartofMolecular Neurobiology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectNeural stem cells (NSC)-
dc.subjectNeurodegeneration-
dc.subjectP73-
dc.subjectNeuronal differentiation-
dc.subjectAlzheimer's disease-
dc.titlep73: A multifunctional protein in neurobiology-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1007/s12035-011-8172-6-
dc.identifier.pmid21380933-
dc.identifier.pmcidPMC3062774-
dc.identifier.scopuseid_2-s2.0-79958706113-
dc.identifier.volume43-
dc.identifier.issue2-
dc.identifier.spage139-
dc.identifier.epage146-
dc.identifier.eissn1559-1182-
dc.identifier.isiWOS:000288714100009-
dc.identifier.issnl0893-7648-

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