NMDA receptor processing in an animal model for schizophrenia

Objective

The pathophysiological mechanisms causing schizophrenia are not well known. Schizophrenia is characterized by symptoms such as hallucinations, emotional isolation and cognitive deficits. Altered neurotransmission through the glutamate transmitter system has been linked to this devastating psychiatric illness. In particular, observations that functional antagonism of the N-methyl-D-apartate (NMDA) glutamate receptor by phencyclidine (PCP) worsens all symptoms in patients and induces a schizophrenia-like psychosis in healthy volunteers have implicated this receptor in schizophrenia. The NMDA receptor, which is principally expressed in postsynaptic spines, is a multimeric protein assembly consisting of the obligatory NR1 subunit in different constellations with NR2A or NR2B subunits. Through alternative splicing of NR1, several regulatory domains are introduced in the receptor, which significantly influence early processing including assembly and forward trafficking. Based on functional divergence, receptors assembled from NR2A and NR2B proteins similarly contribute with functional specialization of the receptor. Studies in postmortem brain indicate that mechanisms associated with early NMDA receptor processing might be altered in schizophrenia. This includes evidence for altered NR1 splicing and compromised trafficking of NR2B-type NMDA receptors. Based on a hypothesis of altered NMDA receptor processing, in this project we will use an animal model to study, in a translational manner, changes in alternative splicing, assembly and trafficking of new NR2A and NR2B receptors in schizophrenia. Furthermore, we will analyze if NMDA receptor processing is modulated by peptides known to enhance cognition. Due to the specialized roles NR2A and NR2B receptors play during complex functions such as cognition, improved understanding of how this receptor system is altered in schizophrenia might lead to improved treatment of symptoms not well treated today.

Fields of science (EuroSciVoc)

CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.

• natural sciences biological sciences biochemistry biomolecules proteins
• medical and health sciences clinical medicine psychiatry schizophrenia

Keywords

Project’s keywords as indicated by the project coordinator. Not to be confused with the EuroSciVoc taxonomy (Fields of science)

• Neurobiology
• alternative splicing
• cognition
• glutamate
• neurotransmission
• postsynaptic density
• protein interaction
• protein synthesis
• receptor assembly

Programme(s)

Multi-annual funding programmes that define the EU’s priorities for research and innovation.

• FP7-PEOPLE - Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)

Topic(s)

Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.

• PEOPLE-2007-4-3.IRG - Marie Curie Action: "International Reintegration Grants"

Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

FP7-PEOPLE-IRG-2008
See other projects for this call

Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

MC-IRG - International Re-integration Grants (IRG)

Coordinator