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Viral-genetic tracing of the input-output organization of a central noradrenaline circuit
Open accessAbstract
Deciphering how neural circuits are anatomically organized with regard to input and output is instrumental in understanding how the brain processes information. For example, locus coeruleus noradrenaline (also known as norepinephrine) (LC-NE) neurons receive input from and send output to broad regions of the brain and spinal cord, and regulate diverse functions including arousal, attention, mood and sensory gating. However, it is unclear how LC-NE neurons divide up their brain-wide projection patterns and whether different LC-NE neurons receive differential input. Here we developed a set of viral-genetic tools to quantitatively analyse the input-output relationship of neural circuits, and applied these tools to dissect the LC-NE circuit in mice. Rabies-virus-based input mapping indicated that LC-NE neurons receive convergent synaptic input from many regions previously identified as sending axons to the locus coeruleus, as well as from newly identified presynaptic partners, including cerebellar Purkinje cells. The 'tracing the relationship between input and output' method (or TRIO method) enables trans-synaptic input tracing from specific subsets of neurons based on their projection and cell type. We found that LC-NE neurons projecting to diverse output regions receive mostly similar input. Projection-based viral labelling revealed that LC-NE neurons projecting to one output region also project to all brain regions we examined. Thus, the LC-NE circuit overall integrates information from, and broadcasts to, many brain regions, consistent with its primary role in regulating brain states. At the same time, we uncovered several levels of specificity in certain LC-NE sub-circuits. These tools for mapping output architecture and input-output relationship are applicable to other neuronal circuits and organisms. More broadly, our viral-genetic approaches provide an efficient intersectional means to target neuronal populations based on cell type and projection pattern.
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“Thus, the input-output architecture of the DR serotonin system differs from that of the locus coeruleus norepinephrine system with more homogeneous input and output (Schwarz et al., 2015), and resembles more closely those of the midbrain dopamine systems (Beier et al., 2015; Lerner et al., 2015), with biased input and segregated output.”
From Anatomically defined and functionally distinct dorsal raphe serotonin sub-systems (2018) · cites this paper as Schwarz et al., 2015
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Cites
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,133
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960
Swanson, L. W., & Hartman, B. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630406 · Cited by 1,475
Whole-Brain Mapping of Direct Inputs to Midbrain Dopamine Neurons
Watabe‐Uchida, M., Zhu, L., Ogawa, S. K., Vamanrao, A., & Uchida, N. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.017 · Cited by 1,277
Monosynaptic Restriction of Transsynaptic Tracing from Single, Genetically Targeted Neurons
Wickersham, I. R., Lyon, D. C., Barnard, R. J. O., Mori, T., Finke, S., Conzelmann, K., Young, J. A. T., & Callaway, E. M. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.033 · Cited by 1,176
Orienting and reorienting: the locus coeruleus mediates cognition through arousal
Sara, S. J., & Bouret, S. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.011 · Cited by 1,056
Tuning arousal with optogenetic modulation of locus coeruleus neurons
Carter, M. E., Yizhar, O., Chikahisa, S., Nguyen, H., Adamantidis, A., Nishino, S., Deisseroth, K., & de Lecea, L. (2010) · Nature Neuroscience · doi:10.1038/nn.2682 · Cited by 993
Gong, S., Doughty, M., Harbaugh, C. R., Cummins, A., Hatten, M. E., Heintz, N., & Gerfen, C. R. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2707-07.2007 · Cited by 977
Genetic Dissection of Neural Circuits
Luo, L., Callaway, E. M., & Svoboda, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.002 · Cited by 771
Self-citationGerfen, C. R., Paletzki, R., & Heintz, N. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.016 · Cited by 647
Afferent projections to the rat locus coeruleus as determined by a retrograde tracing technique
Cedarbaum, J. M., & Aghajanian, G. K. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901780102 · Cited by 553
Cortical representations of olfactory input by trans-synaptic tracing
Miyamichi, K., Amat, F., Moussavi, F., Wang, C., Wickersham, I. R., Wall, N. R., Taniguchi, H., Tasic, B., Huang, Z. J., He, Z., et al. (2010) · Nature · doi:10.1038/nature09714 · Cited by 546
Self-citationAfferent regulation of locus coeruleus neurons: anatomy, physiology and pharmacology
Aston‐Jones, G., Shipley, M., Chouvet, G., Ennis, M. J., Bockstaele, E. V., Pieribone, V. A., Shiekhattar, R., Akaoka, H., Drolet, G., Astier, B., et al. (1991) · Progress in brain research · doi:10.1016/s0079-6123(08)63799-1 · Cited by 543
Functional neuroanatomy of the central noradrenergic system
Szabadi, E. (2013) · Journal of Psychopharmacology · doi:10.1177/0269881113490326 · Cited by 366
Luppi, P., Aston‐Jones, G., Akaoka, H., Chouvet, G., & Jouvet, M. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00481-j · Cited by 344
Heterogeneous organization of the locus coeruleus projections to prefrontal and motor cortices
Chandler, D. J., Gao, W.-J., & Waterhouse, B. D. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320827111 · Cited by 341
Presynaptic partners of dorsal raphe serotonergic and GABAergic neurons
Weissbourd, B., Ren, J., DeLoach, K. E., Guenthner, C. J., Miyamichi, K., & Luo, L. (2014) · Neuron · doi:10.1016/j.neuron.2014.06.024 · Cited by 337
Self-citationMiyamichi, K., Shlomai, Y., Shu, M., Weissbourd, B., Luo, L., & Mizrahi, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.027 · Cited by 309
Self-citationDesign and generation of recombinant rabies virus vectors
Osakada, F., & Callaway, E. M. (2013) · Nature Protocols · doi:10.1038/nprot.2013.094 · Cited by 298
A direct GABAergic output from the basal ganglia to frontal cortex
Saunders, A., Oldenburg, I. A., Berezovskii, V. K., Johnson, C. A., Kingery, N. D., Elliott, H. L., Xie, T., Gerfen, C. R., & Sabatini, B. L. (2015) · Nature · doi:10.1038/nature14179 · Cited by 293
Brain Architecture: Understanding the Basic Plan
Swanson, L. W. (2002) · Cited by 273
Mason, S. T., & Fibiger, H. C. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870405 · Cited by 269
Genetic dissection of the circuit for hand dexterity in primates
Kinoshita, M., Matsui, R., Kato, S., Hasegawa, T., Kasahara, H., Isa, K., Watakabe, A., Yamamori, T., Nishimura, Y., Alstermark, B., et al. (2012) · Nature · doi:10.1038/nature11206 · Cited by 259
Soudais, C., Laplace‐Builhé, C., Kissa, K., & Kremer, E. J. (2001) · The FASEB Journal · doi:10.1096/fj.01-0321fje · Cited by 250
Self-citationDevelopmental origins of central norepinephrine neuron diversity
Robertson, S. D., Plummer, N. W., de Marchena, J., & Jensen, P. (2013) · Nature Neuroscience · doi:10.1038/nn.3458 · Cited by 249
Site-specific integrase-mediated transgenesis in mice via pronuclear injection
Tasic, B., Hippenmeyer, S., Wang, C., Gamboa, M., Zong, H., Chen-Tsai, Y., & Luo, L. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1019507108 · Cited by 246
Self-citationStepien, A. E., Tripodi, M., & Arber, S. (2010) · Neuron · doi:10.1016/j.neuron.2010.10.019 · Cited by 246
Canine Adenovirus Vectors: an Alternative for Adenovirus-Mediated Gene Transfer
Kremer, E. J., Boutin, S., Chillón, M., & Danos, O. (2000) · Journal of Virology · doi:10.1128/jvi.74.1.505-512.2000 · Cited by 245
Self-citationLocus ceruleus and anterior cingulate cortex sustain wakefulness in a novel environment
Gompf, H. S., Mathai, C., Fuller, P. M., Wood, D. A., Pedersen, N. P., Saper, C. B., & Lu, J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.3037-10.2010 · Cited by 176
Hanawa, H., Hematti, P., Keyvanfar, K., Metzger, M. E., Krouse, A. E., Donahue, R. E., Kepes, S., Gray, J. T., Dunbar, C. E., Persons, D. A., et al. (2004) · Blood · doi:10.1182/blood-2004-01-0045 · Cited by 159
Gasser, E. M. S., Straub, C. J., Panzanelli, P., Weinmann, O., Sassoé‐Pognetto, M., & Fritschy, J. (2006) · Nature Protocols · doi:10.1038/nprot.2006.265 · Cited by 132
Highly restricted expression of Cre recombinase in cerebellar Purkinje cells
Zhang, X., Ng, A. H., Tanner, J. A., Wu, W.-T., Copeland, N. G., Jenkins, N. A., & Huang, J. (2004) · genesis · doi:10.1002/gene.20062 · Cited by 124
Divergent axon collaterals of rat locu Demonstration by a fluorescent double labeling technique
Room, P., Postema, F., & Korf, J. (1981) · Brain Research · doi:10.1016/0006-8993(81)90773-3 · Cited by 121
CAR-Associated Vesicular Transport of an Adenovirus in Motor Neuron Axons
Salinas, S., Bilsland, L. G., Henaff, D., Weston, A., Keriel, A., Schiavo, G., & Kremer, E. J. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000442 · Cited by 120
Self-citationNagai, T., Satoh, K., Imamoto, K., & Maeda, T. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90027-6 · Cited by 118
Pivetta, C., Esposito, M. S., Sigrist, M., & Arber, S. (2014) · Cell · doi:10.1016/j.cell.2013.12.014 · Cited by 112
Locus coerules neurons have axons that branch to the forebrain and cerebellum
Steindler, D. A. (1981) · Brain Research · doi:10.1016/0006-8993(81)91149-5 · Cited by 109
Swanson, L. W. (2011) · Oxford University Press eBooks · doi:10.1093/med/9780195378580.001.0001 · Cited by 61
Conchlear inner hair cells exist transiently in the fetal Bronx waltzer (bv/bv) mouse
Whitlon, D. S., Gabel, C., & Zhang, X. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960115)364:3 · Cited by 30
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Joshi, S., Li, Y., Kalwani, R. M., & Gold, J. I. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.028 · Cited by 1,387
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Surmeier, D. J., Obeso, J. A., & Halliday, G. M. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.178 · Cited by 1,116
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Beier, K. T., Steinberg, E. E., DeLoach, K. E., Xie, S., Miyamichi, K., Schwarz, L., Gao, X. J., Kremer, E. J., Malenka, R. C., & Luo, L. (2015) · Cell · doi:10.1016/j.cell.2015.07.015 · Cited by 1,068
Self-citationNeural Circuitry of Wakefulness and Sleep
Scammell, T. E., Arrigoni, E., & Lipton, J. O. (2017) · Neuron · doi:10.1016/j.neuron.2017.01.014 · Cited by 966
Metadata
- Authors
- Schwarz, L. A., Miyamichi, K., Gao, X. J., Beier, K. T., Weissbourd, B., DeLoach, K. E., Ren, J., Ibanes, S., Malenka, R. C., Kremer, E. J., & Luo, L.
- Affiliations
- Howard Hughes Medical Institute (US)
- Centre National de la Recherche Scientifique (FR)
- Stanford Medicine (US)
- Corresponding author
- Luo, Liqun
- ORCID
- Venue
- Nature
- Published
- 2015-07-01
- Volume
- 524
- Issue
- 7563
- Pages
- 88-92
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4587569
- OpenAlex
- W2099401565
- Cited by
- 744
- References
- 40
- Citations by year
- 2026: 48 · 2025: 74 · 2024: 64 · 2023: 85 · 2022: 67 · 2021: 77 · 2020: 85 · 2019: 78 · 2018: 55 · 2017: 55 · 2016: 38 · 2015: 16
- FWCI
- 25.50
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Science Foundation
- Howard Hughes Medical Institute
- Agence Nationale de la Recherche (ANR-10-LABX-0012)
- Stanford Bio-X
- National Institute of Mental Health
- National Institute on Drug Abuse (F32DA038913, P01DA008227)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Keywords
- locus coeruleus, noradrenergic neurons, norepinephrine, rabies virus tracing, transsynaptic tracing, Purkinje cells, neuronal projection patterns, mice, brain states, spinal cord projections, sensory gating
- MeSH terms
- Animals, Axons, Brain, Female, Locus Coeruleus, Male, Neural Pathways, Neurons, Norepinephrine, Pilot Projects, Purkinje Cells, Rabies virus, Synapses, Reproducibility of Results, Rats, Wistar, Mice, Rats, Neuroanatomical Tract-Tracing Techniques
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