Despite many decades of study, schizophrenia remains a poorly understood neurologicaldisorder.However, clinical and experimental studies have implicated dopaminergic, serotoriergic, and glutamatergicneurotransmission in the pathophysiology of this debilitatingpsychiatric disorder. A better understandingof the intracellular signal Iransduction mechanisms linked to these neurotransmitters may more effective treatments for this disease. The responsibilities of the Molecular and Biochemical Core will be to provide a foundation for many of the studies of neuroleptic drug action proposed in Projects 1-5. The Core will perform tasks ranging from sophisticatedscreens that will identify novel protein-protein interactions to basic molecular biology and routine biochemistry that will aid in the investigation these studies. The Core will also provide a technical support facility for the performanceof routine tasks that will be required to accomplish the studies described in Projects 1-5 in an efficient and cosl-effective manner. Thesi tasks will be to maintain stocks of purified protein kinases, protein phosphatases, affinity-purified antibodies, and substrate proteins. Standard purification protocols will be used to obtain these enzymes from native sources, and recombinant technologies will also be employed to produce specific proteins in quantities sufficient to carry out detailed enzymological and structural studies. The Core will also supervise the productionand testing of new polydonal anti-peptide antibodies and phosphorylation state-specific antibodies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH074866-04
Application #
7642297
Study Section
Special Emphasis Panel (ZMH1)
Project Start
Project End
Budget Start
2008-06-01
Budget End
2009-05-31
Support Year
4
Fiscal Year
2008
Total Cost
$159,734
Indirect Cost
Name
Rockefeller University
Department
Type
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Shen, Weixing; Plotkin, Joshua L; Francardo, Veronica et al. (2015) M4 Muscarinic Receptor Signaling Ameliorates Striatal Plasticity Deficits in Models of L-DOPA-Induced Dyskinesia. Neuron 88:762-73
Lee, K-W; Westin, L; Kim, J et al. (2015) Alteration by p11 of mGluR5 localization regulates depression-like behaviors. Mol Psychiatry 20:1546-56
Plotkin, Joshua L; Day, Michelle; Peterson, Jayms D et al. (2014) Impaired TrkB receptor signaling underlies corticostriatal dysfunction in Huntington's disease. Neuron 83:178-88
Görlich, Andreas; Antolin-Fontes, Beatriz; Ables, Jessica L et al. (2013) Reexposure to nicotine during withdrawal increases the pacemaking activity of cholinergic habenular neurons. Proc Natl Acad Sci U S A 110:17077-82
Davis, Maya M; Olausson, Peter; Greengard, Paul et al. (2012) Regulator of calmodulin signaling knockout mice display anxiety-like behavior and motivational deficits. Eur J Neurosci 35:300-8
Park, Jin-Yong; Spruston, Nelson (2012) Synergistic actions of metabotropic acetylcholine and glutamate receptors on the excitability of hippocampal CA1 pyramidal neurons. J Neurosci 32:6081-91
Warner-Schmidt, Jennifer L; Vanover, Kimberly E; Chen, Emily Y et al. (2011) Antidepressant effects of selective serotonin reuptake inhibitors (SSRIs) are attenuated by antiinflammatory drugs in mice and humans. Proc Natl Acad Sci U S A 108:9262-7
Xie, Zhong; Cahill, Michael E; Radulovic, Jelena et al. (2011) Hippocampal phenotypes in kalirin-deficient mice. Mol Cell Neurosci 46:45-54
Plotkin, Joshua L; Day, Michelle; Surmeier, D James (2011) Synaptically driven state transitions in distal dendrites of striatal spiny neurons. Nat Neurosci 14:881-8
Ahn, Jung-Hyuck; Kim, Yong; Kim, Hee-Sun et al. (2011) Protein kinase C-dependent dephosphorylation of tyrosine hydroxylase requires the B56? heterotrimeric form of protein phosphatase 2A. PLoS One 6:e26292

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