C. Vicidomini
POSITIVE MODULATION OF MGLU5 REVERSES ASD-LIKE BEHAVIORS FOUND IN SHANK3 KNOCK-OUT MICE [Tesi di dottorato]
Università degli Studi di Milano, 2016-01-12

Shank proteins are the major scaffold proteins that organize the postsynaptic density at the excitatory synapses. Shank1-3 proteins are associated with type I mGluRs via an interaction with Homer in the proline-rich domain. Phelan-McDermid (PMS) syndrome is characterized by intellectual impairment, absent or delayed speech, and autistic-like behaviors. Loss of Shank3 is now considered to cause the neurobehavioral symptoms of PMS. Furthermore, a significant number of SHANK3 mutations have been identified in patients with Autism Spectrum disorders ASD, and SHANK3 truncating mutations are associated with moderate to profound ID. In this study, we investigated the molecular mechanisms associated with the ASD-like behaviors observed in Shank3Δ11-/- mice in which exon 11 has been deleted. Our results indicate that Shank3 is essential to mediating mGlu5 receptor signaling by recruiting Homer1b/c to the PSD, specifically in the striatum and cortex. Moreover, augmenting mGlu5 receptor activity by administering 3-Cyano-N-(1,3-diphenyl-1H-pyrazol-5-yl)benzamide (CDPPB) ameliorated the functional and behavioral defects that were observed in Shank3Δ11-/- mice, suggesting that pharmaceutical treatments that increase mGlu5 activity may represent a new approach for treating patients that are affected by PMS and SHANK3 mutations.

diritti: info:eu-repo/semantics/openAccess
In relazione con info:eu-repo/semantics/altIdentifier/hdl/2434/353045
SALA, MARIA ELVINA
coordinatore: A. Corsini ; relatore: M. E. Sala ; correlatore: C. Sala
CORSINI, ALBERTO
Settore BIO/14 - - Farmacologia


Tesi di dottorato. | Lingua: Inglese. | Paese: | BID: TD18002327