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The Conserved Dopaminergic Diencephalospinal Tract Mediates Vertebrate Locomotor Development in Zebrafish Larvae
Open accessAbstract
The most conserved part of the vertebrate dopaminergic system is the orthopedia ( otp )-expressing diencephalic neuronal population that constitutes the dopaminergic diencephalospinal tract (DDT). Although studies in the neonatal murine spinal cord in vitro suggest an early locomotor role of the DDT, the function of the DDT in developing vertebrates in vivo remains unknown. Here, we investigated the role of the DDT in the locomotor development of zebrafish larvae. To assess the development of the behavioral and neural locomotor pattern, we used high-throughput video tracking in combination with peripheral nerve recordings. We found a behavioral and neural correspondence in the developmental switch from an immature to mature locomotor pattern. Blocking endogenous dopamine receptor 4 (D 4 R) signaling in vivo either before or after the developmental switch prevented or reversed the switch, respectively. Spinal transections of post-switch larvae reestablished the immature locomotor pattern, which was rescued to a mature-like pattern via spinal D 4 R agonism. Selective chemogenetic ablation of otp b ( otpb ) neurons that contribute to the DDT perpetuated the immature locomotor pattern in vivo . This phenotype was recapitulated by diencephalic transections that removed the dopaminergic otpb population and was rescued to a mature-like locomotor pattern by D 4 R agonism. We conclude that the dopaminergic otpb population, via the DDT, is responsible for spinal D 4 R signaling to mediate the developmental switch to the mature locomotor pattern of zebrafish. These results, integrated with the mammalian literature, suggest that the DDT represents an evolutionarily conserved neuromodulatory system that is necessary for normal vertebrate locomotor development.
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“Blocking D4 dopamine receptors at 3 dpf prevents the transition from burst to beat-and-glide swimming (Lambert et al., 2012), suggesting that dopamine from supraspinal sources plays a role in setting the beat-and-glide phenotype by shortening swimming episode duration.”
From Modeling spinal locomotor circuits for movements in developing zebrafish (2021) · cites this paper as Lambert et al., 2012
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“Beat-and-glide swimming can be produced in isolated larval zebrafish spinal cord preparations by NMDA application (Lambert et al., 2012; McDearmid and Drapeau, 2006; Wiggin et al., 2012) or by optogenetic stimulation of excitatory spinal neurons (Wahlstrom-Helgren et al., 2019).”
From Modeling spinal locomotor circuits for movements in developing zebrafish (2021) · cites this paper as Lambert et al., 2012
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“Blocking D4 dopamine receptors at 3 dpf prevents the transition from burst to beat-and-glide swimming (Lambert et al., 2012), suggesting that dopamine from supraspinal sources plays a role in setting the beat-and-glide phenotype by shortening swimming episode duration.”
From Modeling spinal locomotor circuits for movements in developing zebrafish (2021) · cites this paper as Lambert et al., 2012
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Cites
The Tol2kit: A multisite gateway‐based construction kit for Tol2 transposon transgenesis constructs
Kwan, K. M., Fujimoto, E., Grabher, C., Mangum, B. D., Hardy, M., Campbell, D. S., Parant, J. M., Yost, H. J., Kanki, J. P., & Chien, C.-B. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21343 · Cited by 1,768
Zebrafish Behavioral Profiling Links Drugs to Biological Targets and Rest/Wake Regulation
Rihel, J., Prober, D. A., Arvanites, A. C., Lam, K., Zimmerman, S., Jang, S., Haggarty, S. J., Kokel, D., Rubin, L. L., Peterson, R. T., et al. (2010) · Science · doi:10.1126/science.1183090 · Cited by 795
High-throughput ethomics in large groups of Drosophila
Branson, K. M., Robie, A. A., Bender, J. A., Perona, P., & Dickinson, M. H. (2009) · Nature Methods · doi:10.1038/nmeth.1328 · Cited by 781
Rapid behavior-based identification of neuroactive small molecules in the zebrafish
Kokel, D., Bryan, J., Laggner, C., White, R., Cheung, C. Y. J., Mateus, R., Healey, D., Kim, S. N., Werdich, A. A., Haggarty, S. J., et al. (2010) · Nature Chemical Biology · doi:10.1038/nchembio.307 · Cited by 546
Curado, S., Stainier, D. Y. R., & Anderson, R. M. (2008) · Nature Protocols · doi:10.1038/nprot.2008.58 · Cited by 428
(1998) · doi:10.1016/s0165-0173(98)00016-2 · Cited by 398
Catecholamine systems in the brain of vertebrates: new perspectives through a comparative approach
Smeets, W. J. A. J., & González, A. (2000) · Brain Research Reviews · doi:10.1016/s0165-0173(00)00034-5 · Cited by 385
Tay, T. L., Ronneberger, O., Ryu, S., Nitschke, R., & Driever, W. (2011) · Nature Communications · doi:10.1038/ncomms1171 · Cited by 307
Holzschuh, J., Ryu, S., Aberger, F., & Driever, W. (2001) · Mechanisms of Development · doi:10.1016/s0925-4773(01)00287-8 · Cited by 280
McLean, D. L., & Fetcho, J. R. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20280 · Cited by 267
Müller, U. K., Stamhuis, E. J., & Videler, J. J. (2000) · Journal of Experimental Biology · doi:10.1242/jeb.203.2.193 · Cited by 231
Behavioural assessments of neurotoxic effects and neurodegeneration in zebrafish
Tierney, K. B. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.10.011 · Cited by 218
Orthopedia Homeodomain Protein Is Essential for Diencephalic Dopaminergic Neuron Development
Ryu, S., Mahler, J., Acampora, D., Holzschuh, J., Erhardt, S., Omodei, D., Simeone, A., & Driever, W. (2007) · Current Biology · doi:10.1016/j.cub.2007.04.003 · Cited by 193
Prey capture by larval zebrafish: evidence for fine axial motor control
Borla, M. A., Palecek, B., Budick, S., & O’Malley, D. M. (2002) · Brain, Behavior and Evolution · doi:10.1159/000066699 · Cited by 180 · cited 1×
“A developmental switch in the episodic locomotor pattern from long to short swimming episodes is observed between 3 and 4 days postfertilization (dpf) (Buss and Drapeau, 2001), which is concurrent with increased locomotion and the advent of foraging (Borla et al., 2002).”
BackgroundSynaptic drive to motoneurons during fictive swimming in the developing zebrafish
Buss, R. R., & Drapeau, P. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.1.197 · Cited by 177
Ontogeny of routine swimming activity and performance in zebra danios (Teleostei: Cyprinidae)
Fuiman, L. A., & Webb, P. W. (1988) · Animal Behaviour · doi:10.1016/s0003-3472(88)80268-9 · Cited by 171
Evolution and expression of D2 and D3 dopamine receptor genes in zebrafish
Boehmler, W., Obrecht‐Pflumio, S., Canfield, V. A., Thisse, C., Thisse, B., & Levenson, R. G. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20075 · Cited by 170
Fictive Swimming Motor Patterns in Wild Type and Mutant Larval Zebrafish
Masino, M. A., & Fetcho, J. R. (2005) · Journal of Neurophysiology · doi:10.1152/jn.01248.2004 · Cited by 164
Self-citationBoehmler, W., Carr, T., Thisse, C., Thisse, B., Canfield, V. A., & Levenson, R. G. (2006) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2006.00243.x · Cited by 146
Projections of diencephalic dopamine neurons into the spinal cord in mice
Qu, S., Ondo, W. G., Zhang, X., Xie, W., Pan, T. H., & Le, W. D. (2005) · Experimental Brain Research · doi:10.1007/s00221-005-0075-1 · Cited by 134
Lindsey, B. W., Smith, F. M., & Croll, R. P. (2010) · Zebrafish · doi:10.1089/zeb.2009.0616 · Cited by 130
Endogenous Dopamine Suppresses Initiation of Swimming in Prefeeding Zebrafish Larvae
Thirumalai, V., & Cline, H. T. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90568.2008 · Cited by 128
Brustein, E., Chong, M., Holmqvist, B., & Drapeau, P. (2003) · Journal of Neurobiology · doi:10.1002/neu.10292 · Cited by 126
McLean, D. L., & Fetcho, J. R. (2004) · Journal of Comparative Neurology · doi:10.1002/cne.20281 · Cited by 124
Kastenhuber, E., Kratochwil, C. F., Ryu, S., Schweitzer, J., & Driever, W. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22214 · Cited by 118
Pathophysiological concepts of restless legs syndrome
Paulus, W., Dowling, P., Rijsman, R. M., Stiasny‐Kolster, K., Trenkwalder, C., & de Weerd, A. (2007) · Movement Disorders · doi:10.1002/mds.21533 · Cited by 118
Locomotion Is Increased in A11-Lesioned Mice With Iron Deprivation
Qu, S., Le, W., Zhang, X., Xie, W., Zhang, A., & Ondo, W. G. (2007) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0b013e3180517b5f · Cited by 112
Dopaminergic Modulation of Spinal Neuronal Excitability
Han, P., Nakanishi, S. T., Tran, M. A., & Whelan, P. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1279-07.2007 · Cited by 112
Zhu, H., Clemens, S., Sawchuk, M. A., & Hochman, S. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.07.052 · Cited by 106
Taniguchi, W., Nakatsuka, T., Miyazaki, N., Yamada, H., Takeda, D., Fujita, T., Kumamoto, E., & Yoshida, M. (2010) · Pain · doi:10.1016/j.pain.2010.09.034 · Cited by 105
Zhao, H., Zhu, W., Pan, T., Xie, W., Zhang, A., Ondo, W. G., & Le, W. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21207 · Cited by 104
Antipsychotics produce locomotor impairment in larval zebrafish
Giacomini, N. J., Rose, B. T., Kobayashi, K., & Guo, S. (2006) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2006.01.013 · Cited by 102
Souza, B. R., Romano‐Silva, M. A., & Tropepe, V. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5548-10.2011 · Cited by 84
Nitroreductase-Mediated Cell Ablation in Transgenic Zebrafish Embryos
Pisharath, H., & Parsons, M. J. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-977-2_9 · Cited by 83
Rhythmic motor activity evoked by NMDA in the spinal zebrafish larva
McDearmid, J. R., & Drapeau, P. (2006) · Journal of Neurophysiology · doi:10.1152/jn.00844.2005 · Cited by 79
Motmot, an open-source toolkit for realtime video acquisition and analysis
Straw, A. D., & Dickinson, M. H. (2009) · Source Code for Biology and Medicine · doi:10.1186/1751-0473-4-5 · Cited by 76
Single thalamic dopaminergic neurons project to both the neocortex and spinal cord
Takada, M., Li, Z. K., & Hattori, T. (1988) · Brain Research · doi:10.1016/0006-8993(88)90093-5 · Cited by 68
Farrell, T. C., Cario, C. L., Milanese, C., Vogt, A., Jeong, J., & Burton, E. A. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.05.016 · Cited by 67
Molecular cloning and developmental expression of foxP2 in zebrafish
Bonkowsky, J. L., & Chien, C.-B. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20504 · Cited by 62
Self-citationDomain-specific regulation of foxP2 CNS expression by lef1
Bonkowsky, J. L., Wang, X., Fujimoto, E., Lee, J. E., Chien, C.-B., & Dorsky, R. I. (2008) · BMC Developmental Biology · doi:10.1186/1471-213x-8-103 · Cited by 59
Self-citationDopamine Release in the Prefrontal Cortex and Striatum: Temporal and Behavioural Aspects
Hauber, W. (2010) · Pharmacopsychiatry · doi:10.1055/s-0030-1248300 · Cited by 56
l-DOPA-induced air-stepping in developing rats
Hartesveldt, C. V., Sickles, A. E., Porter, J. D., & Stehouwer, D. J. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90012-8 · Cited by 53
L-DOPA and quipazine elicit air-stepping in neonatal rats with spinal cord transections.
McEwen, M. L., Hartesveldt, C. V., & Stehouwer, D. J. (1997) · Behavioral Neuroscience · doi:10.1037//0735-7044.111.4.825 · Cited by 52
Fujimoto, E., Stevenson, T. J., Chien, C.-B., & Bonkowsky, J. L. (2011) · Developmental Biology · doi:10.1016/j.ydbio.2011.01.023 · Cited by 38
Self-citationDopamine D1 and D2 antagonists block l-DOPA-elicited air-stepping in neonatal rats
Sickles, A. E., Stehouwer, D. J., & Hartesveldt, C. V. (1992) · Developmental Brain Research · doi:10.1016/0165-3806(92)90243-p · Cited by 21
Dopamine D1 and D2 antagonists block l-DOPA-induced air-stepping in decerebrate neonatal rats
McCrea, A. E., Stehouwer, D. J., & Hartesveldt, C. V. (1997) · Developmental Brain Research · doi:10.1016/s0165-3806(97)00027-8 · Cited by 19
Imaging to Differentiate Between Ischemic and Nonischemic Cardiomyopathy
Bax, J. J., Poldermans, D., Schuijf, J. D., Scholte, A. J. H. A., Elhendy, A., & van der Wall, E. E. (2006) · Heart Failure Clinics · doi:10.1016/j.hfc.2006.01.003 · Cited by 8
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- 10.1037/0735-7044.111.4.825 · DOI
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Metadata
- Authors
- Lambert, A. M., Bonkowsky, J. L., & Masino, M. A.
- Affiliations
- University of Minnesota (US)
- University of Utah (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2012-09-26
- Volume
- 32
- Issue
- 39
- Pages
- 13488-13500
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3481997
- OpenAlex
- W2074791476
- Cited by
- 152
- References
- 47
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 6 · 2023: 5 · 2022: 9 · 2021: 13 · 2020: 22 · 2019: 11 · 2018: 13 · 2017: 12 · 2016: 10 · 2015: 12 · 2014: 12 · 2013: 6 · 2012: 1
- FWCI
- 4.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Minnesota
- Vlaamse regering
- National Institutes of Health
- National Institute of Mental Health (DP2MH100008)
- National Institute on Drug Abuse (T32DA022616, K08DA024753)
- National Institute of Neurological Disorders and Stroke (R01NS065054)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- locomotor development, zebrafish larvae, spinal cord, neuromodulation
- MeSH terms
- Analysis of Variance, Animals, Diencephalon, Dopamine, Dose-Response Relationship, Drug, Electrophysiology, Larva, Locomotion, Metronidazole, Neural Pathways, Neurons, Nitroreductases, Peripheral Nervous System Diseases, Peripheral Nerves, Spinal Cord, Transcription Factors, Video Recording, Zebrafish, Dopamine Agents, Signal Transduction, N-Methylaspartate, Excitatory Amino Acid Agonists, In Situ Nick-End Labeling, Zebrafish Proteins, Animals, Genetically Modified, Green Fluorescent Proteins, Receptors, Dopamine D4
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