The overall purpose of this proposal is to examine the role of the estrogen receptor, a nuclear transcription factor, in the differentiation of cerebral cortical circuitry that subserves cognition and undergoes a period of naturally occurring cell death, with features characteristics of apoptosis. The proposed experiments examine the interactions of the estrogen receptor with a family of growth factors, the neurotrophins, in the regulation of this neuronal death within the developing rodent prefrontal/limbic cerebral cortex. We hypothesized that this transcription factor, activated by endogenous growth factors, may selectively alter the process of naturally occurring cell death, and under conditions of inappropriate activation, lead to altered patterns of cortical differentiation. The first specific aim will be to determine whether estrogen receptors mediate the neurotrophin regulation of apoptosis in the developing rodent prefrontal/limbic cerebral cortex. The experimental design will make use of an in vitro explant culture model of chemically induced apoptosis and a complementary in vivo model of naturally occurring apoptosis. The second specific aim will be to determine estrogen receptor-dependent components of the cellular signaling pathway that initiates apoptotic cell death in the cerebral cortex. Specifically, experiments will investigate the estrogen receptor-mediated regulation of specific cyto-protective (i.e., Bcl-2 and Bcl-x) and cytotoxic (TNFr, p75 and fas) components of the signaling pathway that mediate cell survival using in vitro and complementary in vivo models of naturally occurring apoptosis in the developing limbic/prefrontal cerebral cortex. The answers to these questions have clinical implications. Altered activation of transcription factors in the immature cerebral cortex may lead to inappropriate patterns of neuronal survival and differentiation and impairments in the development of cognitive and affective behaviors. Such perturbations may be an important etiologic feature of the impaired functioning characteristics of a variety of psychiatric disorders including schizophrenia and pediatric dementias. Elucidation of basic developmental processes is essential to understanding the pathogenesis of these important psychiatric disorders. Additionally, these experiments will provide a framework for future studies examining the role of the estrogen receptor in cortical plasticity and in the formation of cognitive circuits, integrating the cerebral cortex with its efferent targets.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29MH055724-02
Application #
2416169
Study Section
Molecular, Cellular, and Developmental Neurobiology Review Committee (MCDN)
Program Officer
Leblanc, Gabrielle G
Project Start
1996-08-01
Project End
2001-04-30
Budget Start
1997-05-15
Budget End
1998-04-30
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
City
College Station
State
TX
Country
United States
Zip Code
77845
Cheema, Zulfiqar F; Santillano, Daniel R; Wade, Stephen B et al. (2004) The extracellular matrix, p53 and estrogen compete to regulate cell-surface Fas/Apo-1 suicide receptor expression in proliferating embryonic cerebral cortical precursors, and reciprocally, Fas-ligand modifies estrogen control of cell-cycle proteins. BMC Neurosci 5:11
Cheema, Z F; West, J R; Miranda, R C (2000) Ethanol induces Fas/Apo [apoptosis]-1 mRNA and cell suicide in the developing cerebral cortex. Alcohol Clin Exp Res 24:535-43
McAlhany Jr, R E; West, J R; Miranda, R C (2000) Glial-derived neurotrophic factor (GDNF) prevents ethanol-induced apoptosis and JUN kinase phosphorylation. Brain Res Dev Brain Res 119:209-16
Wade, S B; Oommen, P; Conner, W C et al. (1999) Overlapping and divergent actions of estrogen and the neurotrophins on cell fate and p53-dependent signal transduction in conditionally immortalized cerebral cortical neuroblasts. J Neurosci 19:6994-7006
Cheema, Z F; Wade, S B; Sata, M et al. (1999) Fas/Apo [apoptosis]-1 and associated proteins in the differentiating cerebral cortex: induction of caspase-dependent cell death and activation of NF-kappaB. J Neurosci 19:1754-70
McAlhany Jr, R E; Miranda, R C; Finnell, R H et al. (1999) Ethanol decreases Glial-Derived Neurotrophic Factor (GDNF) protein release but not mRNA expression and increases GDNF-stimulated Shc phosphorylation in the developing cerebellum. Alcohol Clin Exp Res 23:1691-7
McAlhany Jr, R E; West, J R; Miranda, R C (1997) Glial-derived neurotrophic factor rescues calbindin-D28k-immunoreactive neurons in alcohol-treated cerebellar explant cultures. J Neurobiol 33:835-47