Neurotrophins represent an important family of polypeptide growth factors which influence the proliferation, differentiation, survival and death of neuronal and non-neuronal cells during vertebrate development They have been proposed as therapeutic agents for neurodegenerative disorders and nerve injury However, clinical applications have met with very disappointing results, in part due to difficulties of delivery and pharmacokinetics in the nervous system and unanticipated side effects We have found a way to use small molecule ligands of G protein-coupled receptors (GPCR) to activate Trk receptors in the absence of neurotrophin binding These small molecules keep neurons alive by stimulating the actions of trophic factor receptors Ligands for G protein-coupled receptors represent a novel way of stimulating neurotrophin receptor signaling, however, the mechanism of this process is unknown This grant will investigate the cell biological mechanisms that account for transactivation of neurotrophin receptors in neurons and define the contribution of receptor trafficking and transport to this process Defining the proteins that regulate neurotrophin receptor internalization, translocation and signaling is critical to our understanding of normal neuronal development and function as well as perturbations that occur in response to injury or disease. Our findings are directly relevant to the understanding and treatment of neurodegenerative diseases, such as Parkinson's and Alzheimer's diseases and amyotrophic lateral sclerosis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS021072-20
Application #
6829695
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Mamounas, Laura
Project Start
1985-04-01
Project End
2008-11-30
Budget Start
2004-12-01
Budget End
2005-11-30
Support Year
20
Fiscal Year
2005
Total Cost
$401,375
Indirect Cost
Name
New York University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Mitre, Mariela; Mariga, Abigail; Chao, Moses V (2017) Neurotrophin signalling: novel insights into mechanisms and pathophysiology. Clin Sci (Lond) 131:13-23
Linderman, Jessica A; Kobayashi, Mariko; Rayannavar, Vinayak et al. (2017) Immune Escape via a Transient Gene Expression Program Enables Productive Replication of a Latent Pathogen. Cell Rep 18:1312-1323
Ginsberg, Stephen D; Malek-Ahmadi, Michael H; Alldred, Melissa J et al. (2017) Selective decline of neurotrophin and neurotrophin receptor genes within CA1 pyramidal neurons and hippocampus proper: Correlation with cognitive performance and neuropathology in mild cognitive impairment and Alzheimer's disease. Hippocampus :
Bowling, Heather; Bhattacharya, Aditi; Klann, Eric et al. (2016) Deconstructing brain-derived neurotrophic factor actions in adult brain circuits to bridge an existing informational gap in neuro-cell biology. Neural Regen Res 11:363-7
Sleiman, Sama F; Henry, Jeffrey; Al-Haddad, Rami et al. (2016) Exercise promotes the expression of brain derived neurotrophic factor (BDNF) through the action of the ketone body ?-hydroxybutyrate. Elife 5:
Bowling, Heather; Bhattacharya, Aditi; Zhang, Guoan et al. (2016) BONLAC: A combinatorial proteomic technique to measure stimulus-induced translational profiles in brain slices. Neuropharmacology 100:76-89
Mitre, Mariela; Marlin, Bianca J; Schiavo, Jennifer K et al. (2016) A Distributed Network for Social Cognition Enriched for Oxytocin Receptors. J Neurosci 36:2517-35
Anastasia, Agustin; Barker, Phillip A; Chao, Moses V et al. (2015) Detection of p75NTR Trimers: Implications for Receptor Stoichiometry and Activation. J Neurosci 35:11911-20
Daskalakis, Nikolaos P; De Kloet, Edo Ronald; Yehuda, Rachel et al. (2015) Early Life Stress Effects on Glucocorticoid-BDNF Interplay in the Hippocampus. Front Mol Neurosci 8:68
Mariga, Abigail; Glaser, Juliane; Mathias, Leo et al. (2015) Definition of a Bidirectional Activity-Dependent Pathway Involving BDNF and Narp. Cell Rep 13:1747-56

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