Rett syndrome (RTT) is a neurodevelopmental disorder with no efficient treatment that is caused in the majority of cases by mutations in the gene MECP2. RTT becomes manifest after a period of apparently normal development and causes growth deceleration, severe psychomotor impairment and mental retardation. Effective animal models for RTT are available and show morphofunctional abnormalities of synaptic connectivity. However, the molecular consequences of MeCP2 disruption leading to neuronal and synaptic alterations are not known. Protein synthesis regulation via the mammalian target of rapamycin (mTOR) pathway is crucial for synaptic organization and its disruption is involved in a number of neurodevelopmental diseases. We investigated the phosphorylation of the ribosomal protein (rp) S6, whose activation is highly dependent from mTOR activity. Immunohistochemistry showed that rpS6 phosphorylation is severely affected in neurons across cortical areas of Mecp2 mutants and that this alteration precedes the severe symptomatic phase of the disease. Moreover, we found a severe defect of initiation of protein synthesis in the brain of presymptomatic Mecp2 mutant that was not restricted to specific subset of transcripts. Finally, we provide evidence for a general dysfunction of the Akt/mTOR, but not ERK, signaling associated with the disease progression in mutant brains. Our results indicate that defects in Akt/mTOR pathway are responsible for the altered translational control in Mecp2 mutant neurons and disclosed a novel putative biomarker of the pathological process. Importantly, this study provides a novel context of therapeutic interventions that can be designed to successfully restrain or ameliorate the development of RTT.

Reduced AKT/mTOR signaling and protein synthesis dysregulation in a Rett syndrome animal model

BOGGIO, ELENA MARIA;CALCAGNO, ELEONORA;MORELLO, Noemi;GIUSTETTO, Maurizio;
2011

Abstract

Rett syndrome (RTT) is a neurodevelopmental disorder with no efficient treatment that is caused in the majority of cases by mutations in the gene MECP2. RTT becomes manifest after a period of apparently normal development and causes growth deceleration, severe psychomotor impairment and mental retardation. Effective animal models for RTT are available and show morphofunctional abnormalities of synaptic connectivity. However, the molecular consequences of MeCP2 disruption leading to neuronal and synaptic alterations are not known. Protein synthesis regulation via the mammalian target of rapamycin (mTOR) pathway is crucial for synaptic organization and its disruption is involved in a number of neurodevelopmental diseases. We investigated the phosphorylation of the ribosomal protein (rp) S6, whose activation is highly dependent from mTOR activity. Immunohistochemistry showed that rpS6 phosphorylation is severely affected in neurons across cortical areas of Mecp2 mutants and that this alteration precedes the severe symptomatic phase of the disease. Moreover, we found a severe defect of initiation of protein synthesis in the brain of presymptomatic Mecp2 mutant that was not restricted to specific subset of transcripts. Finally, we provide evidence for a general dysfunction of the Akt/mTOR, but not ERK, signaling associated with the disease progression in mutant brains. Our results indicate that defects in Akt/mTOR pathway are responsible for the altered translational control in Mecp2 mutant neurons and disclosed a novel putative biomarker of the pathological process. Importantly, this study provides a novel context of therapeutic interventions that can be designed to successfully restrain or ameliorate the development of RTT.
20(6)
1182
1196
Ricciardi S; Boggio EM; Grosso S; Lonetti G; Forlani G; Stefanelli G; Calcagno E; Morello N; Landsberger N; Biffo S; Pizzorusso T; Giustetto M; Broccoli V
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2318/80777
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