The goal of this project is to understand how the plasticity of adult-born neurons may be harnessed to modify learning and mood regulation. During the training phase (K99) of the award, the candidate augmented his extensive background experience in developmental neurobiology, molecular biology and mouse genetics with a rigorous training in behavioral neuroscience as applied to the study of cognition and emotion in mice. The candidate employed a novel genetic gain of function approach to demonstrate the impact of selectively increasing adult hippocampal neurogenesis on cognition and mood. In the independent (ROO) phase, the candidate will explore the effects of manipulating the properties of adult-born dentate granule neurons, rather than their number, on dentate gyrus dependent functions. The candidate will build on recent work showing that the transcription factor Kruppel-like factor 9 regulates dentate granule neuronal maturation.
The Specific Aims will assess how genetic over expression of Kruppel-like factor 9 in adult neural stem cells and dentate granule neurons influences their maturation and hippocampal functions in normal mice and mouse models of depression. Although a growing literature documents the unique properties of new neurons, how these properties of new neurons relate to fundamental mnemonic processes such as pattern separation and the role of the dentate gyrus in mood regulation is poorly understood. Therefore, the experiments proposed here will attempt to causally link discrete changes in cell-type properties with circuit functions and behavior.

Public Health Relevance

The proposed research will help determine the therapeutic impact of stimulating adult hippocampal neurogenesis for ameliorating cognitive impairments in psychiatric disorders and for treatment of depression. It may result in the development of fast acting novel treatments that target discrete components of adult hippocampal neurogenesis and are encumbered by fewer side effects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Transition Award (R00)
Project #
5R00MH086615-04
Application #
8324287
Study Section
Special Emphasis Panel (NSS)
Program Officer
Winsky, Lois M
Project Start
2009-08-01
Project End
2014-05-31
Budget Start
2012-06-01
Budget End
2013-05-31
Support Year
4
Fiscal Year
2012
Total Cost
$247,356
Indirect Cost
$52,396
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
Ho, N F; Hooker, J M; Sahay, A et al. (2013) In vivo imaging of adult human hippocampal neurogenesis: progress, pitfalls and promise. Mol Psychiatry 18:404-16