Yale School of Medicine

Neurosurgery

Williamson Research, Neurosurgery

Williamson Research, Neurosurgery

Neurosurgery
P.O., Box 208082
New Haven, CT 06520-8082
Tel: 203.785.2805
Fax: 203.785.6916
neurosurgery@yale.edu

Greer Research

Determinants of Local Circuit Organization

Charles A. Greer, Ph.D., Professor, Vice Chairman for Research

Current Research Program

A major goal of my laboratory is understanding the basic mechanisms that contribute to the establishment of orderly topographic maps within the CNS, during both normal development and during regenerative events following injury or disease. We have been focusing our efforts on the olfactory system, in part because of the complexity of the map between the olfactory epithelium and the olfactory bulb. Axons sort into 1,000 functional subsets that are targeted with high specificity to olfactory bulb glomeruli. Using both in vivo and in vitro models, we are currently isolating several mechanisms that may contribute to this complex reorganization including laminin, tenascin and the expression of putative odor receptors in growth cones. In related studies we continue to characterize a unique population of glial cells, ensheathing cells, found in the olfactory nerve. While elsewhere in the mature CNS glia are an impediment to axon growth, the ensheathing cell glia support axon extension and targeting throughout life. We recently demonstrated that the growth promoting effects of ensheathing cells are not limited to olfactory receptor neurons but are also seen in other populations of neurons. Particularly exciting, our recent studies demonstrate that the ensheathing cells remain pluri-potential and that when implanted into demyelinated spinal cord can adopt a myelinating phenotype which remyelinates the axons and contributes to a restoration of normal conduction velocities.

In parallel studies we are examining the molecular and synaptic organization of the olfactory bulb glomeruli. Using RT-PCR we are mapping the distribution of subsets of olfactory receptor cell axons in glomeruli to gain insights into the topography of odor-ligand maps in the olfactory bulb. In addition, working with colleagues, we are using a GFP tag to test hypotheses regarding the specificity of synaptic organization within glomeruli. Second, using antibodies synaptic vesicle related proteins and confocal microscopy we have begun to describe a hitherto unrecognized segregation of local and projection synaptic circuits in the glomeruli. It may be that this segregation underlies the lateral inhibitory systems that are believed to be operative in the olfactory system. Beyond my colleagues in Neurosurgery, I maintain active collaborations with the following Departments at Yale: Neurology, Neurobiology, Anesthesiology and Opthamology. In addition, I have collaborative studies with members of the faculty at Columbia University, Emory University, The Rockefeller, University of Maryland and University of Colorado.

Relationship of Research to Neurological Disease
Increasingly, the neurological sciences are focusing on intervention strategies that will both limit the debilitating consequences of injury/disease as well as increase the probability of successful regeneration of pathways and connections in the CNS. In order to facilitate these processes it is necessary for us to understand the molecular and cellular events operative during axon extension, target selection and synapse formation. The studies described above directly assess those questions and, particularly in the case of the ensheathing cells, offer the possibility of clinical application in the near future. Dr. Greer can be reached at 203-785-4034 or email to charles.greer@yale.edu