Ronald L. Meyer

Professor, Developmental & Cell Biology
School of Biological Sciences

PH.D., California Institute of Technology, 1974

Phone: (949) 824-5565, 6959
Fax: (949) 824-4709
Email: rlmeyer@uci.edu

University of California, Irvine
4101 Natural Sciences II (Office)
4361 Natural Science II (Laboratory)
Mail Code: 2305
Irvine, CA 92697

picture of Ronald L. Meyer

Research
Interests
Regulation of axonal growth, development of nerve connections, nerve injury and regeneration
   
URL devcell.bio.uci.edu/faculty/ronald-meyer/
   
Research
Abstract
Our primary interest is in CNS nerve injury and repair. We are exploring this issue using the visual system. When the optic nerve of a mouse or any other mammal is severed, the nerve fails to regenerate and the animals are permanently blind. However, in goldfish, the severed nerve will regrow back to the brain to restore orderly nerve connections and vision. Much of our current work is focused on understanding how the optic nerve responds to injury and how the neurons in the brain respond to the loss of their nerve connection in the goldfish. In vivo imaging technology using widefield and 2 photon microscopy is used to observe the injured and regenerating axons in the living brain so as to understand the dynamics of their behavior and response to treatments. Electrophysiological recording from the visual centers of the brain is utilized to determine how these neurons compensate for the loss of neuronal input and subsequently adjust to newly formed connections during regeneration.
   
Publications Wu, T., Mohanty, S., Gomez-Godinez, V., Shi, L.Z., Liaw, L.H., Miotke, J., Meyer, R.L., Berns, M.W. (2012) Neuronal growth cones respond to laser-induced axonal damage, J. R. Soc. Interface, 9:535-547.
   
  Wu,T., Nieminen, T.A., Mohanty, S., Miotke, J, Meyer, R.L., Rubinsztein-Dunlop, H., Berns, M.W. (2012) A photon-driven micromotor can direct nerve fiber (axon) growth, Nat. Photonics, 6:62-67.
   
  Dawson, A.J. and Meyer, R.L., (2008) Growth dynamics and morphology of regenerating optic fibers in tectum are altered by injury conditions: An in vivo imaging study in goldfish, Exp. Neurol., 210:592-601
   
  Riegle, K.C. and Meyer, R.L. (2007) Rapid homeostatic plasticity in the intact adult visual system, J. Neurosci. 27: 10556-10567
   
  Si, K, Miotke, J.A., Meyer, R.L., Wang, Z. (2008) Axonal rearrangement without reexpression of a growth associated marker: evidence from the compression of the retinotectal system in adult goldfish, Rest. Neurol. Neurosci., 25:535-547
   
  Miotke, J.A., MacLennan, A.J., Meyer, R.L. (2007) Immunohistochemical localization of CNTFa in adult mouse retina and optic nerve following intraorbital nerve crush: Evidence for the axonal loss of a trophic factor receptor after injury, J. Comp. Neurol. 500: 384-400
   
  Kolls, B.J. and Meyer, R.L. (2002) Spontaneous retinal activity is tonic and does not drive tectal activity during activity-dependent refinement. J. Neurosci. 22:2626-2636
   
  Becker, C.G., Becker, T. and Meyer, R.L. (2001) Increased NCAM-180 immunoreactivity and maintenance of L1 immunoreactivity in injured optic fibers of adult mice. Exp. Neurol. 169: 338-448
   
  Dawson, A.J. and Meyer, R.L. (2001) Regenerating optic fibers correct large-scale errors by random growth: Evidence from in vivo imaging. J. Comp. Neurol. 434:40-55
   
Grants Synaptic Homeostasis in the Visual System, NIH EY013586
   
Reinnervation following sparse regeneration, NIH EY 014200
   
Graduate Programs Neurobiology

Cellular and Molecular Biosciences

   
   
Link to this profile http://www.faculty.uci.edu/profile.cfm?faculty_id=2038
   
Last updated 02/13/2012