The representation and processing of temporal information is an essential component of many cognitive tasks, including the comprehension of spoken language. Patients with cerebellar lesions display problems with both understanding and generating language, and research on human subjects indicates that this cerebellar linguistic deficit may be largely due to a problem in timing. Nonetheless, despite a potential key role for the cerebellum in processing of time, little is known about how cerebellar neurons actually represent and transform temporal information. We propose to develop a novel experimental approach to examine the neural mechanisms of temporal information processing at the microcircuit level. Our goal is to test longstanding hypotheses of the representation of temporal information by the cerebellum, and to derive general principles of temporal processing that will inform understanding of human language comprehension. We will combine two-photon fluorescence microscopy, the delivery of simple auditory stimuli comprising tones and pauses, and an in vivo mouse preparation to examine temporal processing in cerebellar granule cells, the most common but least studied neuron in the brain. Because cerebellar microcircuitry is highly conserved across cerebellar subregions and vertebrate species, our studies in mouse will provide information that is directly relevant to an understanding of human cerebellar function. For over a century, it's been known that cerebellum is important for movement: cerebellar lesions from strokes, genetic mutations, and injuries all can cause ataxia, dysmetria, dysarthria, and tremor, impairing the lives of millions of people worldwide. Patients with many of these symptoms also have impaired timing sensation, including problems with speech and sound perception, arenas where less is known and whose therapy has been less evaluated. Knowledge of the role of the cerebellum in analyzing temporal processing of sound would open up new horizons into the analysis and production of speech. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21DC007902-02
Application #
7168237
Study Section
Cognitive Neuroscience Study Section (COG)
Program Officer
Platt, Christopher
Project Start
2006-01-10
Project End
2009-12-31
Budget Start
2007-01-01
Budget End
2009-12-31
Support Year
2
Fiscal Year
2007
Total Cost
$187,828
Indirect Cost
Name
Stanford University
Department
Physics
Type
Schools of Arts and Sciences
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Nimmerjahn, Axel; Mukamel, Eran A; Schnitzer, Mark J (2009) Motor behavior activates Bergmann glial networks. Neuron 62:400-12
Mukamel, Eran A; Nimmerjahn, Axel; Schnitzer, Mark J (2009) Automated analysis of cellular signals from large-scale calcium imaging data. Neuron 63:747-60
Deisseroth, Karl; Feng, Guoping; Majewska, Ania K et al. (2006) Next-generation optical technologies for illuminating genetically targeted brain circuits. J Neurosci 26:10380-6
Monfared, Ashkan; Blevins, Nikolas H; Cheung, Eunice L M et al. (2006) In vivo imaging of mammalian cochlear blood flow using fluorescence microendoscopy. Otol Neurotol 27:144-52