In particular, Snider and his group are focused on the impact of growth factor molecules on the two types of branching nerve cell components, or processes: axons and dendrites. Axons conduct nervous impulses away from the cell body and its intricately branching dendritic tree. At their terminals, or synapse, axons transmit nerve impulses to other nerve cells or to other 'effector' cells that act by contraction (muscle) or secretion (gland).
"People have known for more than 100 years that if you cut a nerve in the peripheral nervous system, it will re-grow. However, if you damage the spinal cord, no growth whatsoever occurs." Some of his group's experiments have involved genetically altered mice whose axons contain fluorescent proteins for clear visualization of change over time. Several days after injury to an axon within a nerve of the leg, a dramatic increase in the growth factor GDNF is accompanied by axon growth.
On the molecular level, Snider's laboratory is exploring the genetic pathway by which growth factors affect axon growth. He and his group have identified a signal transduction mediator in the growth factor signaling pathways that apparently makes axons rapidly grow longer and also makes them wider.
"We and others have the idea that growth factors are going to be a very important part of axon regeneration," Snider said. "It's our hypothesis that these growth factors actually set up the regenerative response in the peripheral nervous system."
"And if we are able to understand how these growth factors work, we might be able to exploit them to promote regeneration of the spinal cord."
Note: Contact Dr. Snider at 919-843-8623, william_snider@med.unc.edu.
School of Medicine contact Les Lang, 919-843-9687, llang@med.unc.edu
By LESLIE H. LANG
UNC School of Medicine