The degeneration of peripheral sensory axons after injury is an active process regulated by specific intrinsic and extrinsic pathways. I am interested in understanding the mechanisms of peripheral axon degeneration and regeneration, which have important clinical implications but are difficult to study with cellular or molecular resolution in human patients. We have developed a model to study sensory axon degeneration in live zebrafish embryos. Zebrafish are an excellent model for studying neuronal development since they are fertilized externally, develop quickly, and remain transparent for several days post-fertilization, allowing the entire process of neuronal remodeling to be observed in real time in a live organism. Following injury to peripheral sensory axons, the distal portion of the axon that is no longer connected to the cell body quickly breaks down by a process called Wallerian degeneration. The rapid nature of the fragmentation and debris clearance implies that genetic pathways or external influences are responsible for instigating this active response. Our precise laser axotomy technique paired with time-lapse confocal imaging allows for detailed, quantitative analysis of the process of axon degeneration. By understanding and altering the mechanisms of degeneration, it may be possible to improve the ability of an injured axon to regenerate and occupy its previous territory. Alternatively, preventing degeneration from occurring altogether may allow an injured axon to be repaired, thus restoring its function. Any new molecular pathways discovered that affect degeneration could potentially inspire therapies for patients with peripheral nerve damage or acute injury. This proposal focuses primarily on the degeneration of peripheral sensory axons of trigeminal sensory neurons, touch-sensing neurons that innervate the head.
Specific Aim 1 : To determine the intrinsic pathways controlling axon degeneration in different contexts Specific Aim 2: To identify the phagocytes responsible for removing axonal debris in different environments

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31DE019596-03
Application #
8071110
Study Section
NIDCR Special Grants Review Committee (DSR)
Program Officer
Frieden, Leslie A
Project Start
2009-07-01
Project End
2012-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
3
Fiscal Year
2011
Total Cost
$32,402
Indirect Cost
Name
University of California Los Angeles
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095