Development of Neuronal Topography

Department of Biology - Dr. Roger Davenport

Dr. Roger W. Davenport


Department of Biology
Program in Neuroscience and Cognitive Sciences
University of Maryland
College Park, Maryland 20742
email: rd127@umail.umd.edu
phone: (301) 405-8413
fax: (301) 314-9358



Members of the Lab

  • Roger Davenport
  • Research Scientists
  • Mike Dandenault
  • and Technicians:
  • Frank Albert
  • Jobs available
  • Joe Maly
  • immediately




    Research Interests:

    We are interested in determining cellular phenomena that regulate the development of neuronal topography. The underlying cellular and molecular mechanisms that are involved in the formation of the retinotopic and other topographic maps are still poorly understood and remain under active investigation.

    Primarily we examine the development of the retinotectal map in embryonic chick, mouse and rat. We are interested in the cellular interactions which guide retinal ganglion cell (RGC) axons to their target on the optic tectum, axonal branching mechanisms and formation of retinotectal synapses. Ongoing experiments in each of these fields are listed and described in greater detail below




    The chick retinotectal System

    During development of the chick, retinal ganglion cells (RGCs) form specific connections with their target the optic tectum in a highly organized topographic manner. The retinotectal map refers to the coordinate maps of RGC cell bodies across the retinae and their terminations across the tecta. In higher vertebrate, a substantial number of RGC axons project to the ipsilateral optic tecta. In embryonic chick ipsilateral retinotectal projections persists for only approximately one week. The final retinotectal projection in adult chick is almost exclusively contralateral. Nasal RGCs (red, dark blue) will map to the posterior part of the tectum and temporal RGCs (yellow, bright blue) will map to the anterior part. Specific molecules are responsible for the guidance of temporal and nasal fibers across the tectum. Two repellent molecular guidance cues expressed in a gradient across the optic tecta have been determined to be ligands for ephrin tyrosine kinase receptors. Many other factors such as electrical activity might play an important role in axonal pathfinding and much research still needs to be done to elucidate the mechanisms that lead to development of the retinotectal map.


    Research Projects




    Publications



  • Davenport, R.W., E. Thies and M. Cohen. 1999 Neuronal Growth Cone Collapse triggers lateral extensions along trailing axons. Nature Neuroscience; 2(3): 254-259,

  • Rosentreter SM, Davenport RW, Loschinger J, Huf J, Jung J, Bonhoeffer F. 1998 Response of retinal ganglion cell axons to striped linear gradients of repellent guidance molecules. J Neurobiol. 37(4):541-62

  • Davenport, R.W., E. Thies, R. Zhou and P.G. Nelson. 1998 Cellular localization of ephrin-A2, -A5 and other functional guidance cues underlie retinotopic development across species, J Neuroscience, 18(3): 975-986,

  • Davenport, R.W., 1997 Functional guidance components and their cellular distribution in retinotectal co-cultures. Cell and Tissue Research, 290(2): 201-208

  • Davenport, R.W., E. Thies, and P.G. Nelson. 1996. Cellular localization of guidance components in the establishment of retinotectal topography, J Neuroscience, 16(6): 2074-2085.