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dc.contributor.author
Shirazi Fard, Shahrzad
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Kele, Julianna
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Vilar, Marçal
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Paratcha, Gustavo
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Ledda, Maria Fernanda
dc.date.available
2019-01-07T20:08:42Z
dc.date.issued
2010-03
dc.identifier.citation
Shirazi Fard, Shahrzad; Kele, Julianna; Vilar, Marçal; Paratcha, Gustavo; Ledda, Maria Fernanda; Tiam1 as a signaling mediator of Nerve Growth Factor-dependent neurite outgrowth; Public Library of Science; Plos One; 5; 3; 3-2010; 1-11; e9647
dc.identifier.issn
1932-6203
dc.identifier.uri
http://hdl.handle.net/11336/67622
dc.description.abstract
Nerve Growth Factor (NGF)-induced neuronal differentiation requires the activation of members of the Rho family of small GTPases. However, the molecular mechanisms through which NGF regulates cytoskeletal changes and neurite outgrowth are not totally understood. In this work, we identify the Rac1-specific guanine exchange factor (GEF) Tiam1 as a novel mediator of NGF/TrkA-dependent neurite elongation. In particular, we report that knockdown of Tiam1 causes a significant reduction in Rac1 activity and neurite outgrowth induced by NGF. Physical interaction between Tiam1 and active Ras (Ras- GTP), but not tyrosine phosphorylation of Tiam1, plays a central role in Rac1 activation by NGF. In addition, our findings indicate that Ras is required to associate Tiam1 with Rac1 and promote Rac1 activation upon NGF stimulation. Taken together, these findings define a novel molecular mechanism through which Tiam1 mediates TrkA signaling and neurite outgrowth induced by NGF.
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application/pdf
dc.language.iso
eng
dc.publisher
Public Library of Science
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Ngf
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Tiam1
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Neuronal Differentiation
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Rac1 Gtpase
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Otras Medicina Básica
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Medicina Básica
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CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Tiam1 as a signaling mediator of Nerve Growth Factor-dependent neurite outgrowth
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2019-01-07T13:33:46Z
dc.journal.volume
5
dc.journal.number
3
dc.journal.pagination
1-11; e9647
dc.journal.pais
Estados Unidos
dc.journal.ciudad
San Francisco
dc.description.fil
Fil: Shirazi Fard, Shahrzad. Karolinska Huddinge Hospital. Karolinska Institutet; Suecia
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Fil: Kele, Julianna. Karolinska Huddinge Hospital. Karolinska Institutet; Suecia
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Fil: Vilar, Marçal. Universidad de Valencia; España
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Fil: Paratcha, Gustavo. Karolinska Huddinge Hospital. Karolinska Institutet; Suecia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina
dc.description.fil
Fil: Ledda, Maria Fernanda. Karolinska Huddinge Hospital. Karolinska Institutet; Suecia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Biología Celular y Neurociencia "Prof. Eduardo de Robertis". Universidad de Buenos Aires. Facultad de Medicina. Instituto de Biología Celular y Neurociencia; Argentina
dc.journal.title
Plos One
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1371/journal.pone.0009647
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0009647
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