Dendritic spines receive most excitatory synaptic inputs in the brain, and undergo activity-dependent structural changes associated with synaptic plasticity, learning and memory. While changes in the actin cytoskeleton are known to contribute to spine structural remodeling, little attention has been given to the role of microtubules (MTs) in these processes because spines have historically been thought to be devoid of MTs. Recently, MTs have been shown to enter spines in a dynamic, activity-dependent manner, suggesting that they may contribute to post-synaptic plasticity. The proposed experiments will determine the contribution of MTs to spine structural plasticity during long-term potentiation (Aim 1), determine whether MT dynamics are locally regulated by synaptic activity and internal calcium (Aim 2), and determine the contribution of MTs to spine structural plasticity during homeostatic synaptic plasticity (Aim 3). Because almost nothing is currently known about the function of MTs in spines, these studies have the potential to uncover completely novel mechanisms for activity-dependent spine reorganization. This work will have important clinical implications because changes in the dynamics of MTs in dendrites and spines may contribute to abnormal spine and synapse phenotypes associated with degenerative disorders (e.g. Alzheimer's disease), developmental disorders (e.g. Fragile X Syndrome), and psychiatric disorders (e.g. schizophrenia).

Public Health Relevance

Many pathologies of the nervous system, such as Alzheimer's disease and Fragile X Syndrome, alter the structure and motility of dendritic spines and also affect microtubule stability in neurons. This study will determine the contribution of dynamic microtubules to spine morphological plasticity, and will therefore have important implications for diseases that may affect spines, either directly or indirectly, through alterations in microtubule stability.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31NS071816-01
Application #
8003874
Study Section
Special Emphasis Panel (ZRG1-F03A-F (20))
Program Officer
Mamounas, Laura
Project Start
2010-07-01
Project End
2012-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
1
Fiscal Year
2010
Total Cost
$28,270
Indirect Cost
Name
University of Wisconsin Madison
Department
Neurosciences
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Merriam, Elliott B; Millette, Matthew; Lumbard, Derek C et al. (2013) Synaptic regulation of microtubule dynamics in dendritic spines by calcium, F-actin, and drebrin. J Neurosci 33:16471-82
Dent, Erik W; Merriam, Elliott B; Hu, Xindao (2011) The dynamic cytoskeleton: backbone of dendritic spine plasticity. Curr Opin Neurobiol 21:175-81
Merriam, Elliott B; Lumbard, Derek C; Viesselmann, Chris et al. (2011) Dynamic microtubules promote synaptic NMDA receptor-dependent spine enlargement. PLoS One 6:e27688