The Section on Molecular Neuroscience studies the molecular mechanisms of chemically coded ionotropic and metabotropic neurotransmission in in the nervous system. The ultimate goals of the project are identifying signal transduction pathways and trans-acting factors that uniquely control late nervous system phenotypic development, discovering new mammalian neurotransmitters and receptors through examination of the molecular evolution of neurotransmission, and developing ways to understand and restore neurotransmitter balance in animal models of human CNS disease. The following work is in progress in our laboratory:1. Characterization of the ubiquitous secretory protein chromogranin A as a vesiculogenic factor for the generation of large dense-core vesicles (LDCVs) in neuroendocrine cells.2. Development of a neuropeptide-deficient mouse to study the role of classical neurotransmitter-neuropeptide co-transmission through parallel release from small synaptic vesicles (SSVs) and LDCVs in the same peripheral neuron.3. Discovery of a combinatorial signaling system activated by the neuropeptide PACAP that targets the VIP gene in neuroendocrine cells through two novel pathways involving calcineurin and cAMP-dependent/protein kinase A-independent signaling, respectively. 4. Characterization of the unique co-expression of prostaglandin synthetic enzymes in cholinergic neurons of the primate, compared to the rodent, cholinergic projection neurons of the nucleus basalis of Meynert.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Intramural Research (Z01)
Project #
1Z01MH002386-14
Application #
6432806
Study Section
(LCMR)
Project Start
Project End
Budget Start
Budget End
Support Year
14
Fiscal Year
2000
Total Cost
Indirect Cost
Name
U.S. National Institute of Mental Health
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Emery, Andrew C; Xu, Wenqin; Eiden, Maribeth V et al. (2017) Guanine nucleotide exchange factor Epac2-dependent activation of the GTP-binding protein Rap2A mediates cAMP-dependent growth arrest in neuroendocrine cells. J Biol Chem 292:12220-12231
Emery, Andrew C; Alvarez, Ryan A; Eiden, Maribeth V et al. (2017) Differential Pharmacophore Definition of the cAMP Binding Sites of Neuritogenic cAMP Sensor-Rapgef2, Protein Kinase A, and Exchange Protein Activated by cAMP in Neuroendocrine Cells Using an Adenine-Based Scaffold. ACS Chem Neurosci 8:1500-1509
Jenkins, Danielle E; Sreenivasan, Dharshini; Carman, Fiona et al. (2016) Interleukin-6-mediated signaling in adrenal medullary chromaffin cells. J Neurochem 139:1138-1150
Jiang, Sunny Zhihong; Eiden, Lee E (2016) Activation of the HPA axis and depression of feeding behavior induced by restraint stress are separately regulated by PACAPergic neurotransmission in the mouse. Stress 19:374-82
Emery, Andrew C; Alvarez, Ryan A; Abboud, Philip et al. (2016) C-terminal amidation of PACAP-38 and PACAP-27 is dispensable for biological activity at the PAC1 receptor. Peptides 79:39-48
Schütz, Burkhard; Schäfer, Martin K-H; Gördes, Markus et al. (2015) Satb2-independent acquisition of the cholinergic sudomotor phenotype in rodents. Cell Mol Neurobiol 35:205-16
Mustafa, Tomris (2013) Pituitary adenylate cyclase-activating polypeptide (PACAP): a master regulator in central and peripheral stress responses. Adv Pharmacol 68:445-57
Samal, Babru; Ait-Ali, Djida; Bunn, Stephen et al. (2013) Discrete signal transduction pathway utilization by a neuropeptide (PACAP) and a cytokine (TNF-alpha) first messenger in chromaffin cells, inferred from coupled transcriptome-promoter analysis of regulated gene cohorts. Peptides 45:48-60
Schäfer, M K-H; Hartwig, N R; Kalmbach, N et al. (2013) Species-specific vesicular monoamine transporter 2 (VMAT2) expression in mammalian pancreatic beta cells: implications for optimising radioligand-based human beta cell mass (BCM) imaging in animal models. Diabetologia 56:1047-56
Smith, Corey B; Eiden, Lee E (2012) Is PACAP the major neurotransmitter for stress transduction at the adrenomedullary synapse? J Mol Neurosci 48:403-12

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