Protein kinase c activation drives a ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
URL permanente :
Titre :
Protein kinase c activation drives a differentiation program in an oligodendroglial precursor model through the modulation of specific biological networks
Auteur(s) :
Damato, Marina [Auteur]
Università del Salento = University of Salento [Lecce]
Cardon, Tristan [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Wisztorski (Admin), Maxence [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Fournier, Isabelle [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Pieragostino, Damiana [Auteur]
Università degli studi "G. d'Annunzio" Chieti-Pescara [Chieti-Pescara] [Ud'A]
Cicalini, Ilaria [Auteur]
Università degli studi "G. d'Annunzio" Chieti-Pescara [Chieti-Pescara] [Ud'A]
Salzet, Michel [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Vergara, Daniele [Auteur]
Università del Salento = University of Salento [Lecce]
Maffia, Michele [Auteur]
Università del Salento = University of Salento [Lecce]
Università del Salento = University of Salento [Lecce]
Cardon, Tristan [Auteur]

Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Wisztorski (Admin), Maxence [Auteur]

Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Fournier, Isabelle [Auteur]

Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Pieragostino, Damiana [Auteur]
Università degli studi "G. d'Annunzio" Chieti-Pescara [Chieti-Pescara] [Ud'A]
Cicalini, Ilaria [Auteur]
Università degli studi "G. d'Annunzio" Chieti-Pescara [Chieti-Pescara] [Ud'A]
Salzet, Michel [Auteur]

Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Vergara, Daniele [Auteur]
Università del Salento = University of Salento [Lecce]
Maffia, Michele [Auteur]
Università del Salento = University of Salento [Lecce]
Titre de la revue :
International Journal of Molecular Sciences
Nom court de la revue :
Int J Mol Sci
Numéro :
22
Pagination :
5245
Date de publication :
2021-05-15
ISSN :
1422-0067
Mot(s)-clé(s) :
PKC
differentiation
ROCK
cytoskeleton
mass spectrometry
signaling
oligodendrocytes
differentiation
ROCK
cytoskeleton
mass spectrometry
signaling
oligodendrocytes
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Protein kinase C (PKC) activation induces cellular reprogramming and differentiation in various cell models. Although many effectors of PKC physiological actions have been elucidated, the molecular mechanisms regulating ...
Lire la suite >Protein kinase C (PKC) activation induces cellular reprogramming and differentiation in various cell models. Although many effectors of PKC physiological actions have been elucidated, the molecular mechanisms regulating oligodendrocyte differentiation after PKC activation are still unclear. Here, we applied a liquid chromatography-mass spectrometry (LC-MS/MS) approach to provide a comprehensive analysis of the proteome expression changes in the MO3.13 oligodendroglial cell line after PKC activation. Our findings suggest that multiple networks that communicate and coordinate with each other may finally determine the fate of MO3.13 cells, thus identifying a modular and functional biological structure. In this work, we provide a detailed description of these networks and their participating components and interactions. Such assembly allows perturbing each module, thus describing its physiological significance in the differentiation program. We applied this approach by targeting the Rho-associated protein kinase (ROCK) in PKC-activated cells. Overall, our findings provide a resource for elucidating the PKC-mediated network modules that contribute to a more robust knowledge of the molecular dynamics leading to this cell fate transition.Lire moins >
Lire la suite >Protein kinase C (PKC) activation induces cellular reprogramming and differentiation in various cell models. Although many effectors of PKC physiological actions have been elucidated, the molecular mechanisms regulating oligodendrocyte differentiation after PKC activation are still unclear. Here, we applied a liquid chromatography-mass spectrometry (LC-MS/MS) approach to provide a comprehensive analysis of the proteome expression changes in the MO3.13 oligodendroglial cell line after PKC activation. Our findings suggest that multiple networks that communicate and coordinate with each other may finally determine the fate of MO3.13 cells, thus identifying a modular and functional biological structure. In this work, we provide a detailed description of these networks and their participating components and interactions. Such assembly allows perturbing each module, thus describing its physiological significance in the differentiation program. We applied this approach by targeting the Rho-associated protein kinase (ROCK) in PKC-activated cells. Overall, our findings provide a resource for elucidating the PKC-mediated network modules that contribute to a more robust knowledge of the molecular dynamics leading to this cell fate transition.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
INSERM
Université de Lille
Université de Lille
Date de dépôt :
2022-06-15T14:00:13Z
2023-02-01T10:43:15Z
2023-02-01T10:43:15Z
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- ijms-22-05245-v3.pdf
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