Michael P. Nusbaum, Ph.D.  

photo Michael Nusbaum

Professor of Neuroscience

Chair
Neuroscience Graduate Group

Office: 120 Johnson Pavilion
Tel: 215-898-1585
Fax: 215-573-9050
Email:   nusbaum@mail.med.upenn.edu


Mailing Address:
Department of Neuroscience
School of Medicine
215 Stemmler Hall
University of Pennsylvania
Philadelphia, PA 19104/6074

 


RESEARCH INTEREST

Neural network modulation; motor pattern selection from multifunctional networks; local, presynaptic influences; neuropeptide function, cotransmission, sensory influence on central neuronal networks.


RESEARCH TECHNIQUES

Intrasomatic and intra-axonal recordings, extracellular recordings, intracellular dye injections, neurotransmitter immunocytochemistry; exogenous application of modulatory transmitters; confocal microscopy.


RESEARCH SUMMARY

We aim to understand how the nervous system selects and generates distinct motor patterns from multifunctional neural networks. The current set of issues that we are addressing include (1) the cellular mechanisms underlying how different identified modulatory projection and sensory neurons elicit distinct outputs from the same neural circuits, including the role of coreleased small molecule and neuropeptide transmitters in this process, and (2) how distinct but related neural circuits interact to generate a coordinated output. We use a small model system, the stomatogastric nervous system (STNS), which is an extension of the CNS in decapod crustaceans that controls the rhythmic movements of different regions of the foregut underlying various aspects of feeding. The STNS consists of 4 ganglia, containing several distinct but interacting rhythmically active circuits that control the different foregut regions. The two motor patterns that we study (called the pyloric and gastric mill rhythms) are generated by overlapping sets of neurons located in the stomatogastric ganglion (STG), which contains only 26 neurons in our experimental animal, the crab Cancer borealis. There are many advantages to studying this preparation for obtaining a cellular-level understanding of neuronal circuit function. All of the STG neurons are readily recorded intracellularly, they are all physiologically identified, their intraganglionic synapses and many of their membrane properties are known, and so are their neurotransmitters. More than a dozen modulatory transmitters have been localized as inputs to the STG from the other STNS ganglia. When individually bath applied, many of these transmitters elicit distinct pyloric and gastric mill rhythms. Individual activation of different projection and sensory neurons also elicits distinct rhythms. We are using a set of identified projection and sensory neurons to study the above-mentioned issues. We are also assessing the relationship between the circuit response to bath application of individual modulatory transmitters and to activation of modulatory neurons containing the same transmitter. Our analysis also includes identifying and determining the function of "presynaptic inputs" occurring on the STG terminals of these projection neurons. These presynaptic inputs are electrically invisible in the ganglion of origin of these neurons, so we study them by recording from these neurons intra-axonally, at the entrance to the STG. Results from work with the STNS has led to general principles of neural circuit dynamics that have been extended to many other systems, ranging from other invertebrates to the mammalian systems.

KEY WORDS:   Neuromodulation; neural networks; neuropeptides; identified neurons; cotransmission.

KEY REFERENCES


Blitz DM, Beenhakker MP, Nusbaum MP (2004) Different sensory systems share projection neurons but elicit distinct motor patterns. J Neurosci 24:11381-11390

Beenhakker MP, Nusbaum MP (2004) Mechanosensory activation of a motor circuit by coactivation of two projection neurons. J Neurosci 24:6741-6750.

Wood DE, Manor Y, Nadim F, Nusbaum MP (2004) Inter-circuit control via rhythmic regulation of projection neuron activity. J Neurosci, 24:7455-7463.

Beenhakker MP, Blitz DM, Nusbaum MP (2004) Long-lasting activation of rhythmic neuronal activity by a novel mechanosensory system in the crustacean stomatogastric nervous system. Journal of Neurophysiology 91:78-91.

Christie AE, Stein W, Quinlan JE, Beenhakker MP, Marder E, Nusbaum MP (2004) Actions of a histaminergic/peptidergic projection neuron on rhythmic motor patterns in the stomatogastric nervous system of the crab Cancer borealis. Journal of Comparative Neurology 469:153-169.

Nusbaum MP (2002) Regulating peptidergic modulation of rhythmically active neural circuits. Brain Behavior and Evolution 60:378-387.

Wood DE, Nusbaum MP (2002) Extracellular peptidase activity tunes motor pattern modulation. J Neurosci 22:4185-4195.

Nusbaum MP, Beenhakker MP (2002) A small-systems approach to motor pattern generation. Nature 417:343-350.

Nusbaum MP, Blitz DM, Swensen AM, Wood DE, Marder E (2001) The roles of cotransmission in neural network modulation. Trends Neurosci 24:146-154.

Swensen AM, Golowasch J, Christie AE, Coleman MJ, Nusbaum MP, Marder E (2000) GABA and GABA responses in the stomatogastric ganglion of the crab. Cancer borealis. J Exp Biol, 203:2075-2092.

Meyrand P, Faumont S, Simmers J, Christie AE, Nusbaum MP (2000) Species-specific modulation of pattern-generating circuits. European J Neurosci 12:2585-2596.

Wood DE, Stein W, Nusbaum MP (2000) Projection neurons with shared cotransmitters elicit different motor patterns from the same neural circuit. J Neurosci 20:8943-8953.

Blitz DM, Christie AE, Coleman MJ, Norris BJ, Marder E, Nusbaum MP (1999) Different proctolin neurons elicit distinct motor patterns from a multifunctional neuronal network. J Neurosci 19:5449-5463.

Bartos M, Manor Y, Nadim F, Marder E, Nusbaum MP (1999) Coordination of fast and slow rhythmic neuronal circuits. J Neurosci 19:6650-6660.

Blitz DM, Nusbaum MP (1999) Distinct functions for cotransmitters mediating motor pattern selection. J Neurosci 19:6774-6783.