Injury to the spinal cord initiates a complex cascade of events, the net effect of which is a behaviorally limiting neurological deficit. Innumerable investigations of spinal cord injury have led to the realization that in order to improve the neurological outcome of patients we must first understand the basic mechanisms that promote differentiation and growth in the developing nervous system and regeneration and repair in the adult. This program project is designed as a coordinated effort to identify basic cellular mechanisms influencing degeneration and regeneration in the CNS following injury. The ultimate goal of the proposed studies is to develop a body of knowledge sufficient for identifying and understanding basic mechanisms which may be susceptible to intervention strategies leading to an improvement in neurological outcome. The program is divided into 6 major areas: 1) A core facility providing for electronmicroscopy studies; 2) A core facility providing for administrative support; 3) Studies focussed on trophic factors and membrane components that may influence regeneration; 4) Analyses of mechanisms influencing sprouting and reactive synaptogenesis; 5) Characterization of functional capacities of regenerating neurons including the activity of voltage-dependent channels; and 6) Cytochemical and genetic mechanisms underlying regeneration and the role of the genome in reactivating specific developmental genes potentially important in regenerative responses. These studies will fill critical gaps in our current understanding of regenerative responses in the developing and adult CNS. This knowledge is not only crucial for the development of successful strategies for treating spinal cord injury but also for injuries elsewhere in the CNS as well as disease processes involving the progressive loss of populations of neurons such as occurs in Alzheimer's dementia.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS010174-18
Application #
3107581
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1978-09-01
Project End
1992-08-31
Budget Start
1989-09-01
Budget End
1990-08-31
Support Year
18
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Yale University
Department
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Radtke, Christine; Akiyama, Yukinori; Brokaw, Jane et al. (2004) Remyelination of the nonhuman primate spinal cord by transplantation of H-transferase transgenic adult pig olfactory ensheathing cells. FASEB J 18:335-7
Liu, Chang-Ning; Devor, Marshall; Waxman, Stephen G et al. (2002) Subthreshold oscillations induced by spinal nerve injury in dissociated muscle and cutaneous afferents of mouse DRG. J Neurophysiol 87:2009-17
Akiyama, Yukinori; Radtke, Christine; Honmou, Osamu et al. (2002) Remyelination of the spinal cord following intravenous delivery of bone marrow cells. Glia 39:229-36
Akiyama, Yukinori; Radtke, Christine; Kocsis, Jeffery D (2002) Remyelination of the rat spinal cord by transplantation of identified bone marrow stromal cells. J Neurosci 22:6623-30
Lankford, Karen L; Imaizumi, Toshio; Honmou, Osamu et al. (2002) A quantitative morphometric analysis of rat spinal cord remyelination following transplantation of allogenic Schwann cells. J Comp Neurol 443:259-74
Everill, B; Cummins, T R; Waxman, S G et al. (2001) Sodium currents of large (Abeta-type) adult cutaneous afferent dorsal root ganglion neurons display rapid recovery from inactivation before and after axotomy. Neuroscience 106:161-9
Sasaki, M; Honmou, O; Akiyama, Y et al. (2001) Transplantation of an acutely isolated bone marrow fraction repairs demyelinated adult rat spinal cord axons. Glia 35:26-34
Kohama, I; Lankford, K L; Preiningerova, J et al. (2001) Transplantation of cryopreserved adult human Schwann cells enhances axonal conduction in demyelinated spinal cord. J Neurosci 21:944-50
Yan, H; Nie, X; Kocsis, J D (2001) Hepatocyte growth factor is a mitogen for olfactory ensheathing cells. J Neurosci Res 66:698-704
Imaizumi, T; Lankford, K L; Kocsis, J D (2000) Transplantation of olfactory ensheathing cells or Schwann cells restores rapid and secure conduction across the transected spinal cord. Brain Res 854:70-8

Showing the most recent 10 out of 34 publications