Journal
NATURE NEUROSCIENCE
Volume 13, Issue 3, Pages 327-U12Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nn.2487
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Funding
- US National Institutes of Health [MH-084018, MH-069853, MH-088753, MH-071316, MH-084233, NS-048911]
- Stanley
- Cure Huntington's Disease Initiative
- HighQ
- S R Foundation
- RUSK
- National Alliance for Research on Schizophrenia and Depression
- National Alliance for Autism Research
- Medical Research Council [G0600765]
- European Union [LSHB-CT-2006-037189]
- Medical Research Council [G0600765] Funding Source: researchfish
- Grants-in-Aid for Scientific Research [22791125] Funding Source: KAKEN
- MRC [G0600765] Funding Source: UKRI
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Synaptic spines are dynamic structures that regulate neuronal responsiveness and plasticity. We examined the role of the schizophrenia risk factor DISC1 in the maintenance of spine morphology and function. We found that DISC1 anchored Kalirin-7 (Kal-7), regulating access of Kal-7 to Rac1 and controlling the duration and intensity of Rac1 activation in response to NMDA receptor activation in both cortical cultures and rat brain in vivo. These results explain why Rac1 and its activator (Kal-7) serve as important mediators of spine enlargement and why constitutive Rac1 activation decreases spine size. This mechanism likely underlies disturbances in glutamatergic neurotransmission that have been frequently reported in schizophrenia that can lead to alteration of dendritic spines with consequential major pathological changes in brain function. Furthermore, the concept of a signalosome involving disease-associated factors, such as DISC1 and glutamate, may well contribute to the multifactorial and polygenetic characteristics of schizophrenia.
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