Candice C. Askwith, Ph.D.

Assistant Professor
Department of Neuroscience

Degree: University of Utah
Postdoctoral Training: University of Iowa, Dr. Michael J. Welsh

Contact Information
4066C Graves Hall
333 W. 10th Avenue
Columbus, OH  43210
PHONE: (614) 292-9366
FAX: (614) 688-8742
E-MAIL: askwith.1@osu.edu

Link to NLM PubMed publications list for Candice C. Askwith (last 10 years)

Research Area:

Ion channels in synaptic plasticity and sensory transduction: Acid-sensing ion channel (ASIC) function, structure, and role in synaptic physiology.

Current Research:

Ion channels produce the electrical signals that are critical for the transmission, reception, and integration of information in the nervous system. Acid-sensing ion channels (ASICs) open with the application of acidic solutions and generate voltage-insensitive sodium currents in many neurons. ASICs are thought to play a role in conditions where the extracellular pH falls such as ischemia, seizures, and inflammation. Mice with disruptions in individual ASIC subunits have altered sensory transduction and deficits in behaviors linked to learning and memory. This indicates that ASICs are required for normal neuronal physiology and suggests that pH fluctuations and proton-gated currents play an important role throughout the nervous system.

ASICs localize to synapses and it is thought that protons released from synaptic vesicles activate ASICs. Our goal is to understand the mechanism of ASIC activation in vivo and determine how ASICs affects synaptic physiology. We are using whole-cell patch-clamp analysis to define the contribution of ASICs to proton-gated currents and synaptic transmission in cultured neurons. We are also investigating which channel characteristics are important for ASIC function with transgenic mice and mutant ASIC channels.

FMRFamide-related neuropeptides interact directly with ASIC channels and modulate their activity. However, the physiological consequences of this interaction are unknown. Using structure/function analysis, we are defining the protein domains responsible for neuropeptide potentiation in ASICs and will investigate the involvement of ASICs and FMRFamide using behavioral assays in mice. Given that ASICs and FMRFamide-related neuropeptides are both up-regulated during inflammation and both play a role in nociception, this interaction may play an important role in pain.

Techniques:

• Molecular Biology: RT-PCR, site-directed mutagenesis, cDNA cloning, RNA isolation, Northern and Southern blotting.
• Cell Biology: mammalian cell transfection, Western blotting, immunoprecipitation, primary neuronal cultures, immunocytochemistry.
• Transgenic: Production and analysis of transgenic mice in conjunction with the Transgenic Mouse Facility at the Neurobiotechnology Center, maintenance of knockout mouse lines, mouse behavioral assays.
• Electrophysiology: Two-electrode voltage-clamp in Xenopus oocytes, patch-clamp analysis in neurons and mammalian cell lines.