The intent of this application is to request funds for the training minority students in the field of developmental neurobiology. The main objective of the proposal, in which the students will be involved, is to examine factors that regulates the development and expression of neurotransmitter phenotypes in the central nervous system (CNS) of the chick. In our current MBRS grant period we sought to establish the chick embryo as an experimental model for such development studies, and completed an extensive analysis of the ontogenesis of central serotonergic (5-HT) neurons in the brain and spinal cord. The information provided by these pervious studies serves as a basis for the present proposal which includes the following specific aims: (1) An immunocytochemical description of the initial development of several additional transmitter phenotypes in the chick CNS. The phenotypes selected for study are of interest because of their possible co-existence with 5-HT neuronal systems. (2) A further examination of the regulation of the expression of the 5-HT phenotype in a unique population of 5- HT neurons intrinsic to the spinal cord. Of interest are the changes in the number of cells expressing this phenotype during embryonic and post-hatching development. (3) An initial attempt to manipulate the expression of these spinal cord 5-HT neurons during development utilizing in vitro cultures of dissociated spinal cord cells and in ovo microsurgical techniques. The overall intent of these studies is to define the timing and potential mechanisms responsible for neurotransmitter phenotype determination, expression and possible plasticity in the chick CNS. The exposure of undergraduate minority students to the exciting field of development neurobiology and to the various current techniques proposed for use in this application will hopefully encourage their consideration of continuing their education and training for careers in biomedical research.

Project Start
Project End
Budget Start
Budget End
Support Year
17
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of New Mexico
Department
Type
DUNS #
829868723
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Bharadwaj, D; Mold, C; Markham, E et al. (2001) Serum amyloid P component binds to Fc gamma receptors and opsonizes particles for phagocytosis. J Immunol 166:6735-41
Romero, I R; Morris, C; Rodriguez, M et al. (1998) Inflammatory potential of C-reactive protein complexes compared to immune complexes. Clin Immunol Immunopathol 87:155-62
Tetzloff, S U; Bizzozero, O A (1998) Palmitoylation of proteolipid protein from rat brain myelin using endogenously generated 18O-fatty acids. J Biol Chem 273:279-85
Sanchez, P; Tetzloff, S U; Bizzozero, O A (1998) Veratridine-induced depolarization reduces the palmitoylation of brain and myelin glycerolipids. J Neurochem 70:1448-57
Bryant, J E; Hutchings, K G; Moyzis, R K et al. (1997) Measurement of telomeric DNA content in human tissues. Biotechniques 23:476-8, 480, 482, passim
Melendez, R F; Bizzozero, O A (1996) Palmitoylation of myelin P0 protein is independent of its synthesis and parallels that of phospholipids. J Peripher Nerv Syst 1:34-41
Mold, C; Gurule, C; Otero, D et al. (1996) Complement-dependent binding of C-reactive protein complexes to human erythrocyte CR1. Clin Immunol Immunopathol 81:153-60
Chapin, J E; Davis, L E; Kornfeld, M et al. (1995) Neurologic manifestations of intravascular lymphomatosis. Acta Neurol Scand 91:494-9
Smith, J P; Hicks, P S; Ortiz, L R et al. (1995) Quantitative measurement of muscle strength in the mouse. J Neurosci Methods 62:15-9
Varela, M F; Sansom, C E; Griffith, J K (1995) Mutational analysis and molecular modelling of an amino acid sequence motif conserved in antiporters but not symporters in a transporter superfamily. Mol Membr Biol 12:313-9

Showing the most recent 10 out of 18 publications