Department of Neuroscience


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Home > People > Faculty > Chen Gu, Ph. D.
 
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Candice C. Askwith, Ph. D.
Christine E. Beattie, Ph.D.
Georgia A. Bishop, Ph.D.
R. Thomas Boyd, Ph.D
Anthony Brown, Ph.D.
Richard W. Burry, Ph.D.
Helen J. Cooke, Ph.D.
Andrey V. Dmitriev, Ph.D.
John J. Enyeart, Ph.D.
Andy J. Fischer, Ph.D.
Chen Gu, Ph. D.
Paul D. Henion, Ph.D.
James D. Jontes Ph. D
C. Glenn Lin, Ph.D.
Stuart C. Mangel Ph.D.
Dana M McTigue, Ph.D.
John D. Oberdick, Ph.D.
Karl Obrietan, Ph.D.
Christophe P. Ribelayga, Ph.D.
Mike Xi Zhu, Ph.D.
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Chen Gu, Ph. D.

Assistant Professor

Department of Neuroscience and Center for Molecular Neurobiology

Degree: University of Colorado Health Sciences Center
Postdoctoral Training: University of California San Francisco

Phone: (614) 292-0349
Fax: (614) 292-5379
Email: gu.49@osu.edu   

Link to NLM PubMed publications list for Chen Gu (last 10 years)



 

Research Area:


Ion channel trafficking and neurological disease
.

 

Current Research:


Precise targeting of ion channels into distinct subcellular domains is essential for neuronal electrical signaling. Altered electrical signaling caused by mis-targeting or malfunction of ion channels can induce clinical symptoms in neurological diseases. We are interested in studying the molecular mechanisms underlying and pathophysiological significance of ion channel trafficking. Currently, we are focusing on the following two projects.

1. Molecular mechanism underlying the axonal targeting of voltage-gated potassium (Kv) channels. Dendrite and axon are two prominent polarized structures of neurons, responsible for the input and output of electrical signals. Axonal Kv channels control the waveform and speed of action potentials that convey signals along axons from somatodendritic regions to nerve terminals. We are pursuing the intra-neuronal mechanisms governing axonal targeting of these channels.

2. Targeting and function of ion channels in myelinated axons. Axon and myelinating glia exhibit remarkable cell-cell interactions during development. Crucial for the saltatory conduction and synchronized presynaptic input, myelin limits axonal ion channels into distinct membrane domains along axons, for instance voltage- gated sodium channels at the nodes of Ranvier, Kv1 channels in the juxtaparanodal regions. We are investigating how the external factor (from myelin) regulates ion channel axonal targeting, and how this regulation is involved in demyelinating diseases, such as multiple sclerosis.

Techniques and Models:

 

Molecular Biology: PCR, site-directed mutagenesis, fluorescent protein fusion, siRNA knockdown, Western blotting, protein purification, immunoprecipitation.


Cell Biology: primary neuronal culture, neuron-glia co-culture, transfection, viral infection, immunocytochemistry.

Imaging: multi-color time lapse, fluorescence resonance energy transfer (FRET), total internal reflection fluorescence (TIRF).


Animal model: murine experimental autoimmune encephalomyelitis (EAE).