Mark Masino, PhD
Associate Professor, Department of Neuroscience
Electrophysiology, Optical Imaging of Calcium Activity, Confocal Microscopy, Behavior
Central pattern generators
Most rhythmic motor patterns in animals, including breathing, chewing, limbed locomotion, and undulatory swimming are programmed in part by neural circuits called central pattern generators. These pattern generators often have, at their core, rhythmically active neurons or neural networks. The study of these pattern generators has yielded insight not only into the origins of rhythmic activity, but also into the functioning and modulation of neural networks in general. My primary interest is to understand how spinal circuits are structurally and functionally organized to generate different rhythmic motor patterns. In vertebrates, neural circuits are located in spinal cord and mediate rhythmic movements by the activation of spinal motor neurons via premotor interneurons. Therefore, different movements must, in part, be determined by the differences in activity of the spinal premotor interneurons. To understand how different motor behaviors are produced by spinal circuits, it is critical to determine:
- Which classes of interneuron are involved in specific behaviors.
- The synaptic connectivity pattern in spinal circuits.
- The patterns of activity in identified classes during different behaviors.
- The intrinsic and modulated membrane and channel properties of the neurons invovled in the pattern generating circuit.
- How perturbation of a circuit changes the behavior.
Until recently these issues have been difficult to address in vertebrate preparations because of the complexity of the spinal cord, the inability to monitor activity in identified classes of interneuron during different behaviors, the lack of appropriate genetic tools, and the difficulty in performing perturbation experiments. However, the larval zebrafish model system is an outstanding candidate to begin to address these questions. First, investigation of identified neurons and thus neural circuits is a tenable endeavor since there are a limited number of neurons in the spinal cord. Second, genetic and molecular tools have matured so that the identification and labeling of particular classes of interneurons is routine. Third, the translucent nature of the preparation combined with conventional or genetically encoded indicators makes it particularly appropriate for optical methods of investigation. Thus, optical imaging can be used to monitor activity in particular classes of interneuron during behavior. Finally, perturbation experiments can be used to examine the functional role of a particular class of interneuron in behavior, which may provide insights into the functional organization of spinal circuits. Therefore, my intent is to exploit the convergence of these tools in studies which address the functional organization of spinal interneurons involved in generating different patterns of motor activity.
Tye, M & Masino, MA 2019, 'Dietary contaminants and their effects on zebrafish embryos', Toxics, vol. 7, no. 3, 46. https://doi.org/10.3390/toxics7030046
Wahlstrom-Helgren, S, Montgomery, JE, Vanpelt, KT, Biltz, SL, Peck, JH & Masino, MA 2019, 'Glutamate receptor subtypes differentially contribute to optogenetically activated swimming in spinally transected zebrafish larvae', Journal of neurophysiology, vol. 122, no. 6, pp. 2414-2426. https://doi.org/10.1152/jn.00337.2019
Montgomery, JE, Wahlstrom-Helgren, S, Wiggin, TD, Corwin, BM, Lillesaar, C & Masino, MA 2018, 'Intraspinal serotonergic signaling suppresses locomotor activity in larval zebrafish', Developmental Neurobiology, vol. 78, no. 8, pp. 807-827. https://doi.org/10.1002/dneu.22606
Tye, MT, Montgomery, JE, Hobbs, MR, Vanpelt, KT & Masino, MA 2018, 'An Adult Zebrafish Diet Contaminated with Chromium Reduces the Viability of Progeny' Zebrafish, vol. 15, no. 2, pp. 179-187. https://doi.org/10.1089/zeb.2017.1514
Montgomery, JE, Wahlstrom-Helgren, S, Wiggin, TD, Corwin, BM, Lillesaar, C & Masino, MA 2018, 'Intraspinal serotonergic signaling suppresses locomotor activity in larval zebrafish' Developmental Neurobiology. https://doi.org/10.1002/dneu.22606
Montgomery, JE, Wiggin, TD, Rivera-Perez, LM, Lillesaar, C & Masino, MA 2016, 'Intraspinal serotonergic neurons consist of two, temporally distinct populations in developing zebrafish' Developmental Neurobiology, vol. 76, no. 6, pp. 673-687. https://doi.org/10.1002/dneu.22352
Wiggin, TD, Peck, JH & Masino, MA 2014, 'Coordination of fictive motor activity in the larval zebrafish is generated by non-segmental mechanisms' PLoS One, vol. 9, no. 10, 0109117. https://doi.org/10.1371/journal.pone.0109117
Decker, AR, McNeill, MS, Lambert, AM, Overton, JD, Chen, YC, Lorca, RA, Johnson, NA, Brockerhoff, SE, Mohapatra, DP, MacArthur, H, Panula, P, Masino, MA, Runnels, LW & Cornell, RA 2014, 'Abnormal differentiation of dopaminergic neurons in zebrafish trpm7 mutant larvae impairs development of the motor pattern' Developmental Biology, vol. 386, no. 2, pp. 428-439. https://doi.org/10.1016/j.ydbio.2013.11.015
Ingebretson, JJ & Masino, MA 2013, 'Quantification of locomotor activity in larval Zebrafish: Considerations for the design of high-throughput behavioral studies' Frontiers in Neural Circuits, no. MAY. https://doi.org/10.3389/fncir.2013.00109
Puhl, JG, Masino, MA & Mesce, KA 2012, 'Necessary, sufficient and permissive: A single locomotor command neuron important for intersegmental coordination' Journal of Neuroscience, vol. 32, no. 49, pp. 17646-17657. https://doi.org/10.1523/JNEUROSCI.2249-12.2012
NSC 5661: Behavioral Neuroscience (Spring semester)