Bone morphogenetic proteins (BMPs) have been implicated as control factors in many different developmental transitions. During nervous system development BMPs regulate neural induction, formation of the neural crest, and the development of both neurons and glia. Within individual neural lineages, BMPs control progressive developmental decisions, reflecting changes in cellular responses to BMPs over time. In the peripheral nervous system BMPs increase neuronal differentiation of neural crest cells and later promote the maturation of enteric and sympathetic neurons along lineage-specific pathways. The goal of this proposal is to determine the cellular and molecular mechanisms underlying the developmental actions of BMPs during the divergence of the enteric and sympathetic nervous systems and to investigate the basis of changing BMP responsiveness. We will determine the role of BMPs in regulating developmental transitions of multipotent precursor cells, committed neuronal progenitors, and developing glial cells. We will test the hypothesis that BMP2 promotes neuronal differentiation by maintaining a pool of uncommitted precursor cells at the expense of glial differentiation and that BMP signaling contributes to the timing of neuron and glial development in the peripheral nervous system. A role for BMPs in the divergence of the enteric and sympathetic lineages and the maturation of specific neuronal subtypes will be examined and we will test the idea that BMP signaling contributes to the acquisition of functional neuronal properties in vitro and in the animal. BMP responses depend upon the pattern of transcriptional activation set up through expression of specific transcription factors. We will use DNA microarrays to define BMP-induced changes in patterns of transcription factor gene expression at different developmental stages. The integration of cellular and transcriptional analysis of BMP function and the use of a novel inducible transgenic mouse system for the regulation of BMP signaling in vivo will result in a new understanding of the regulatory circuits that contribute to the divergence and maturation of peripheral neuron lineages.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD042716-01A2
Application #
6724532
Study Section
Molecular, Cellular and Developmental Neurosciences 2 (MDCN)
Program Officer
Henken, Deborah B
Project Start
2003-12-01
Project End
2008-11-30
Budget Start
2003-12-01
Budget End
2004-11-30
Support Year
1
Fiscal Year
2004
Total Cost
$328,761
Indirect Cost
Name
Brandeis University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02454
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Luther, Jason A; Birren, Susan J (2009) Neurotrophins and target interactions in the development and regulation of sympathetic neuron electrical and synaptic properties. Auton Neurosci 151:46-60
Luther, Jason A; Birren, Susan J (2009) p75 and TrkA signaling regulates sympathetic neuronal firing patterns via differential modulation of voltage-gated currents. J Neurosci 29:5411-24
Dore, Justin J; DeWitt, John C; Setty, Nithya et al. (2009) Multiple signaling pathways converge to regulate bone-morphogenetic-protein-dependent glial gene expression. Dev Neurosci 31:473-86
Habecker, Beth A; Bilimoria, Parizad; Linick, Camille et al. (2008) Regulation of cardiac innervation and function via the p75 neurotrophin receptor. Auton Neurosci 140:40-8
Moon, Jung-Il; Birren, Susan J (2008) Target-dependent inhibition of sympathetic neuron growth via modulation of a BMP signaling pathway. Dev Biol 315:404-17
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Dore, Justin J; Crotty, Kate L; Birren, Susan J (2005) Inhibition of glial maturation by bone morphogenetic protein 2 in a neural crest-derived cell line. Dev Neurosci 27:37-48