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.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The input-output architecture of the DR serotonin system differs from the locus coeruleus norepinephrine system with more homogeneous input and output, and resembles midbrain dopamine systems with biased input and segregated output.
“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
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
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 · see citing works
Dahlstroem, A., & Fuxé, K. (1964) · PubMed · Cited by 5,143 · see citing works
Aston-Jones, G., & Bloom, F. (1981) · The Journal of Neuroscience · doi:10.1523/jneurosci.01-08-00876.1981 · Cited by 1,960 · see citing works
Swanson, L. W., & Hartman, B. K. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901630406 · Cited by 1,479 · see citing works
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 1,221 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Genetic Dissection of Neural Circuits
Luo, L., Callaway, E. M., & Svoboda, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.002 · Cited by 754 · see citing works
Self-citationGerfen, C. R., Paletzki, R., & Heintz, N. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.016 · Cited by 647 · see citing works
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 549 · see citing works
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 · see citing works
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 · see citing works
Luppi, P., Aston‐Jones, G., Akaoka, H., Chouvet, G., & Jouvet, M. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00481-j · Cited by 344 · see citing works
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 · see citing works
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 · see citing works
Self-citationFunctional neuroanatomy of the central noradrenergic system
Szabadi, E. (2013) · Journal of Psychopharmacology · doi:10.1177/0269881113490326 · Cited by 337 · see citing works
Miyamichi, K., Shlomai, Y., Shu, M., Weissbourd, B., Luo, L., & Mizrahi, A. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.027 · Cited by 310 · see citing works
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 296 · see citing works
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 · see citing works
Brain Architecture: Understanding the Basic Plan
Swanson, L. W. (2002) · Cited by 273 · see citing works
Mason, S. T., & Fibiger, H. C. (1979) · The Journal of Comparative Neurology · doi:10.1002/cne.901870405 · Cited by 264 · see citing works
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 262 · see citing works
Self-citationGenetic 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 · see citing works
Soudais, C., Laplace‐Builhé, C., Kissa, K., & Kremer, E. J. (2001) · The FASEB Journal · doi:10.1096/fj.01-0321fje · Cited by 250 · see citing works
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 · see citing works
Stepien, A. E., Tripodi, M., & Arber, S. (2010) · Neuron · doi:10.1016/j.neuron.2010.10.019 · Cited by 246 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
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 · see citing works
Self-citationNagai, T., Satoh, K., Imamoto, K., & Maeda, T. (1981) · Neuroscience Letters · doi:10.1016/0304-3940(81)90027-6 · Cited by 118 · see citing works
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 · see citing works
Pivetta, C., Esposito, M. S., Sigrist, M., & Arber, S. (2014) · Cell · doi:10.1016/j.cell.2013.12.014 · Cited by 106 · see citing works
Swanson, L. W. (2011) · Oxford University Press eBooks · doi:10.1093/med/9780195378580.001.0001 · Cited by 62 · see citing works
Roberts, V. J., Barth, S., Meunier, H., & Vale, W. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960115)364:3 · Cited by 45 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Chan, K. Y., Jang, M. J., Yoo, B. B., Greenbaum, A., Ravi, N., Wu, W.-L., Sánchez-Guardado, L., Lois, C., Mazmanian, S. K., Deverman, B. E., et al. (2017) · Nature Neuroscience · doi:10.1038/nn.4593 · Cited by 1,578 · see citing works
Joshi, S., Li, Y., Kalwani, R. M., & Gold, J. I. (2016) · Neuron · doi:10.1016/j.neuron.2015.11.028 · Cited by 1,387 · see citing works
Selective neuronal vulnerability in Parkinson disease
Surmeier, D. J., Obeso, J. A., & Halliday, G. M. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2016.178 · Cited by 1,120 · see citing works
Circuit architecture of VTA dopamine neurons revealed by systematic input-output mapping
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 · see citing works
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 · see citing works
Locus coeruleus and dopaminergic consolidation of everyday memory
Takeuchi, T., Duszkiewicz, A. J., Sonneborn, A., Spooner, P. A., Yamasaki, M., Watanabe, M., Smith, C. C., Fernández, G., Deisseroth, K., Greene, R. W., et al. (2016) · Nature · doi:10.1038/nature19325 · Cited by 827 · see citing works
Intact-brain analyses reveal distinct information carried by SNc dopamine subcircuits
Lerner, T. N., Shilyansky, C., Davidson, T. J., Evans, K. E., Beier, K. T., Zalocusky, K. A., Crow, A. K., Malenka, R. C., Luo, L., Tomer, R., et al. (2015) · Cell · doi:10.1016/j.cell.2015.07.014 · Cited by 794 · see citing works
“…CLARITY-optimized light-sheet microscopy (COLM) (Chung et al., 2013; Tomer et al., 2014), along with a variation of rabies-based circuit mapping (Schwarz et al., 2015); the lattermethod (TRIO) operates similarly to previously published rabies-based circuit mapping technologies, utilizing a…”
MethodSelf-citationZingg, B., Chou, X.-L., Zhang, Z., Mesik, L., Liang, F., Tao, H. W., & Zhang, L. I. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.045 · Cited by 744 · see citing works
Locus coeruleus: a new look at the blue spot
Poe, G. R., Foote, S., Eschenko, O., Johansen, J. P., Bouret, S., Aston-Jones, G., Harley, C. W., Manahan-Vaughan, D., Weinshenker, D., Valentino, R., et al. (2020) · Nature Reviews Neuroscience · doi:10.1038/s41583-020-0360-9 · Cited by 720 · see citing works
Integration of optogenetics with complementary methodologies in systems neuroscience
Kim, C. K., Adhikari, A., & Deisseroth, K. (2017) · Nature reviews. Neuroscience · doi:10.1038/nrn.2017.15 · Cited by 690 · see citing works
Organization of the Locus Coeruleus-Norepinephrine System
Schwarz, L. A., & Luo, L. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.039 · Cited by 578 · see citing works
Self-citationA genetically encoded fluorescent sensor for rapid and specific in vivo detection of norepinephrine
Feng, J., Zhang, C., Lischinsky, J. E., Jing, M., Zhou, J., Wang, H., Zhang, Y., Dong, A., Wu, Z., Wu, H., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.037 · Cited by 545 · see citing works
Neurobiological links between stress and anxiety
Daviu, N., Bruchas, M. R., Moghaddam, B., Sandi, C., & Beyeler, A. (2019) · Neurobiology of Stress · doi:10.1016/j.ynstr.2019.100191 · Cited by 528 · see citing works
Light Affects Mood and Learning through Distinct Retina-Brain Pathways
Fernandez, D. C., Fogerson, P. M., Lazzerini Ospri, L., Thomsen, M. B., Layne, R. M., Severin, D., Zhan, J., Singer, J. H., Kirkwood, A., Zhao, H., et al. (2018) · Cell · doi:10.1016/j.cell.2018.08.004 · Cited by 505 · see citing works
Anatomically defined and functionally distinct dorsal raphe serotonin sub-systems
Ren, J., Friedmann, D., Xiong, J., Liu, C. D., Ferguson, B. R., Weerakkody, T., DeLoach, K. E., Ran, C., Pun, A., Sun, Y., et al. (2018) · Cell · doi:10.1016/j.cell.2018.07.043 · Cited by 498 · see citing works
Self-citationCerebellar granule cells encode the expectation of reward
Wagner, M. J., Kim, T. H., Savall, J., Schnitzer, M. J., & Luo, L. (2017) · Nature · doi:10.1038/nature21726 · Cited by 485 · see citing works
Self-citationFunctional circuit architecture underlying parental behaviour
Kohl, J., Babayan, B. M., Rubinstein, N. D., Autry, A. E., Marin-Rodriguez, B., Kapoor, V., Miyamichi, K., Zweifel, L. S., Luo, L., Uchida, N., et al. (2018) · Nature · doi:10.1038/s41586-018-0027-0 · Cited by 459 · see citing works
Self-citationGenetic Dissection of Neural Circuits: A Decade of Progress
Luo, L., Callaway, E. M., & Svoboda, K. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.040 · Cited by 446 · see citing works
Self-citationMonosynaptic Circuit Tracing with Glycoprotein-Deleted Rabies Viruses
Callaway, E. M., & Luo, L. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0409-15.2015 · Cited by 418 · see citing works
Self-citationEliava, M., Melchior, M., Knobloch-Bollmann, H. S., Wahis, J., da Silva Gouveia, M., Tang, Y., Ciobanu, A. C., Triana del Rio, R., Roth, L. C., Althammer, F., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.041 · Cited by 409 · see citing works
Architectures of neuronal circuits
Luo, L. (2021) · Science · doi:10.1126/science.abg7285 · Cited by 390 · see citing works
Self-citationNeuromodulation by the immune system: a focus on cytokines
Salvador, A. F., de Lima, K. A., & Kipnis, J. (2021) · Nature Reviews Immunology · doi:10.1038/s41577-021-00508-z · Cited by 389 · see citing works
High-throughput mapping of single-neuron projections by sequencing of barcoded RNA
Kebschull, J. M., Garcia da Silva, P., Reid, A. P., Peikon, I. D., Albeanu, D. F., & Zador, A. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.036 · Cited by 376 · see citing works
Farmer, A. D., Strzelczyk, A., Finisguerra, A., Gourine, A. V., Gharabaghi, A., Hasan, A., Burger, A. M., Jaramillo, A. M., Mertens, A., Majid, A., et al. (2021) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2020.568051 · Cited by 361 · see citing works
A Brainstem-Spinal Cord Inhibitory Circuit for Mechanical Pain Modulation by GABA and Enkephalins
François, A., Low, S. A., Sypek, E. I., Christensen, A. J., Sotoudeh, C., Beier, K. T., Ramakrishnan, C., Ritola, K., Sharif‐Naeini, R., Deisseroth, K. A., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.01.008 · Cited by 354 · see citing works
Self-citationActive control of arousal by a locus coeruleus GABAergic circuit
Breton‐Provencher, V., & Sur, M. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0305-z · Cited by 348 · see citing works
Modular organization of the brainstem noradrenaline system coordinates opposing learning states
Uematsu, A., Tan, B. Z., Ycu, E. A., Cuevas, J. N. S., Koivumaa, J., Junyent, F., Kremer, E. J., Witten, I. B., Deisseroth, K. A., & Johansen, J. P. (2017) · Nature Neuroscience · doi:10.1038/nn.4642 · Cited by 331 · see citing works
Self-citationLocus coeruleus to basolateral amygdala noradrenergic projections promote anxiety-like behavior
McCall, J. G., Siuda, E. R., Bhatti, D. L., Lawson, L. A., McElligott, Z. A., Stuber, G. D., & Bruchas, M. R. (2017) · eLife · doi:10.7554/elife.18247 · Cited by 322 · see citing works
Rapid Reconfiguration of the Functional Connectome after Chemogenetic Locus Coeruleus Activation
Zerbi, V., Floriou‐Servou, A., Markicevic, M., Vermeiren, Y., Sturman, O., Privitera, M., von Ziegler, L., Ferrari, K. D., Weber, B., Deyn, P. P. D., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.034 · Cited by 322 · see citing works
Susaki, E. A., & Ueda, H. R. (2016) · Cell chemical biology · doi:10.1016/j.chembiol.2015.11.009 · Cited by 297 · see citing works
Breathing control center neurons that promote arousal in mice
Yackle, K., Schwarz, L. A., Kam, K., Sorokin, J. M., Huguenard, J. R., Feldman, J. L., Luo, L., & Krasnow, M. A. (2017) · Science · doi:10.1126/science.aai7984 · Cited by 282 · see citing works
Self-citationDistinct Ventral Pallidal Neural Populations Mediate Separate Symptoms of Depression
Knowland, D., Lilascharoen, V., Pacia, C. P., Shin, S., Wang, E. H.-J., & Lim, B. K. (2017) · Cell · doi:10.1016/j.cell.2017.06.015 · Cited by 273 · see citing works
Locus coeruleus: From global projection system to adaptive regulation of behavior
Aston‐Jones, G., & Waterhouse, B. D. (2016) · Brain Research · doi:10.1016/j.brainres.2016.03.001 · Cited by 268 · see citing works
Cellular anatomy of the mouse primary motor cortex
Muñoz-Castañeda, R., Zingg, B., Matho, K. S., Chen, X., Wang, Q., Foster, N. N., Li, A., Narasimhan, A., Hirokawa, K. E., Huo, B., et al. (2021) · Nature · doi:10.1038/s41586-021-03970-w · Cited by 262 · see citing works
Central amygdala circuits modulate food consumption through a positive-valence mechanism
Douglass, A. M., Kucukdereli, H., Ponserre, M., Marković, M., Gründemann, J., Strobel, C., Morales, P. L. A., Conzelmann, K., Lüthi, A., & Klein, R. (2017) · Nature Neuroscience · doi:10.1038/nn.4623 · Cited by 257 · see citing works
Dendritic spines: Revisiting the physiological role
Chidambaram, S. B., Rathipriya, A. G., Bolla, S. R., Bhat, A., Ray, B., Mahalakshmi, A. M., Manivasagam, T., Thenmozhi, A. J., Essa, M. M., Guillemin, G. J., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.01.005 · Cited by 255 · see citing works
Locus coeruleus norepinephrine activity mediates sensory-evoked awakenings from sleep
Hayat, H., Regev, N., Matosevich, N., Sales, A. C., Paredes-Rodriguez, E., Krom, A. J., Bergman, L., Li, Y., Lavigne, M., Kremer, E. J., et al. (2020) · Science Advances · doi:10.1126/sciadv.aaz4232 · Cited by 255 · see citing works
Self-citationHu, H. (2016) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070815-014106 · Cited by 253 · see citing works
Cerebellar nuclei evolved by repeatedly duplicating a conserved cell-type set
Kebschull, J. M., Richman, E. B., Ringach, N., Friedmann, D., Albarran, E., Kolluru, S. S., Jones, R. C., Allen, W. E., Wang, Y., Cho, S. W., et al. (2020) · Science · doi:10.1126/science.abd5059 · Cited by 253 · see citing works
Self-citationHirschberg, S., Li, Y., Randall, A. D., Kremer, E. J., & Pickering, A. E. (2017) · eLife · doi:10.7554/elife.29808 · Cited by 252 · see citing works
Self-citationFujita, H., Kodama, T., & du Lac, S. (2020) · eLife · doi:10.7554/elife.58613 · Cited by 239 · see citing works
The emergence and influence of internal states
Flavell, S. W., Gogolla, N., Lovett-Barron, M., & Zelikowsky, M. (2022) · Neuron · doi:10.1016/j.neuron.2022.04.030 · Cited by 234 · see citing works
The Input-Output Relationship of the Cholinergic Basal Forebrain
Gielow, M. R., & Záborszky, L. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.060 · Cited by 230 · see citing works
Rorabaugh, J. M., Chalermpalanupap, T., Botz-Zapp, C. A., Fu, V. M., Lembeck, N. A., Cohen, R. M., & Weinshenker, D. (2017) · Brain · doi:10.1093/brain/awx232 · Cited by 227 · see citing works
Chandler, D. J., Jensen, P., McCall, J. G., Pickering, A. E., Schwarz, L. A., & Totah, N. K. B. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1164-19.2019 · Cited by 215 · see citing works
Self-citationA VTA GABAergic Neural Circuit Mediates Visually Evoked Innate Defensive Responses
Zhou, Z., Liu, X., Chen, S., Zhang, Z., Liu, Y., Montardy, Q., Tang, Y., Wei, P., Liu, N., Li, L., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.027 · Cited by 211 · see citing works
The diversity of GABAergic neurons and neural communication elements
Huang, Z. J., & Paul, A. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0195-4 · Cited by 201 · see citing works
Dorsal Striatal Circuits for Habits, Compulsions and Addictions
Lipton, D. M., Gonzales, B. J., & Citri, A. (2019) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2019.00028 · Cited by 197 · see citing works
Noradrenergic Modulation of Fear Conditioning and Extinction
Giustino, T. F., & Maren, S. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00043 · Cited by 189 · see citing works
Synaptic Specificity and Application of Anterograde Transsynaptic AAV for Probing Neural Circuitry
Zingg, B., Peng, B., Huang, J., Tao, H. W., & Zhang, L. I. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2158-19.2020 · Cited by 189 · see citing works
Parkinson's Disease Is Not Simply a Prion Disorder
Surmeier, D. J., Obeso, J. A., & Halliday, G. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1787-16.2017 · Cited by 186 · see citing works
A labeled-line neural circuit for pheromone-mediated sexual behaviors in mice
Ishii, K. K., Osakada, T., Mori, H., Miyasaka, N., Yoshihara, Y., Miyamichi, K., & Touhara, K. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.038 · Cited by 185 · see citing works
Self-citationThe Locus Coeruleus Is a Complex and Differentiated Neuromodulatory System
Totah, N. K., Neves, R. M., Panzeri, S., Logothetis, N. K., & Eschenko, O. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.037 · Cited by 179 · see citing works
Shared cortex-cerebellum dynamics in the execution and learning of a motor task
Wagner, M. J., Kim, T. H., Kadmon, J., Nguyen, N. D., Ganguli, S., Schnitzer, M. J., & Luo, L. (2019) · Cell · doi:10.1016/j.cell.2019.02.019 · Cited by 177 · see citing works
Self-citationSun, Q., Li, X., Ren, M., Zhao, M., Zhong, Q., Ren, Y., Luo, P., Ni, H., Zhang, X., Zhang, C., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0429-9 · Cited by 175 · see citing works
The Role of the Locus Coeruleus in Pain and Associated Stress-Related Disorders
Suárez‐Pereira, I., Llorca-Torralba, M., Bravo, L., Camarena-Delgado, C., Soriano‐Mas, C., & Berrocoso, E. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.11.023 · Cited by 174 · see citing works
Nontoxic, double-deletion-mutant rabies viral vectors for retrograde targeting of projection neurons
Chatterjee, S., Sullivan, H. A., MacLennan, B. J., Xu, R., Hou, Y., Lavin, T. K., Lea, N. E., Michalski, J. E., Babcock, K. R., Dietrich, S., et al. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0091-7 · Cited by 172 · see citing works
Breton‐Provencher, V., Drummond, G. T., & Sur, M. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.638007 · Cited by 172 · see citing works
Viral Strategies for Targeting the Central and Peripheral Nervous Systems
Bedbrook, C. N., Deverman, B. E., & Gradinaru, V. (2018) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080317-062048 · Cited by 168 · see citing works
Osorio-Forero, A., Foustoukos, G., Cardis, R., Cherrad, N., Devenoges, C., Fernandez, L. M. J., & Lüthi, A. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01822-0 · Cited by 166 · see citing works
Neuronal circuits in barrel cortex for whisker sensory perception
Staiger, J. F., & Petersen, C. C. H. (2021) · Physiological Reviews · doi:10.1152/physrev.00019.2019 · Cited by 165 · see citing works
Neuromodulation in circuits of aversive emotional learning
Likhtik, E., & Johansen, J. P. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0503-3 · Cited by 165 · see citing works
The Noradrenergic System in Parkinson’s Disease
Paredes-Rodriguez, E., Vegas‐Suárez, S., Morera‐Herreras, T., Deurwaerdère, P. D., & Miguélez, C. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.00435 · Cited by 165 · see citing works
Consensus Paper: Experimental Neurostimulation of the Cerebellum
Miterko, L. N., Baker, K. B., Beckinghausen, J., Bradnam, L. V., Cheng, M., Cooperrider, J., DeLong, M. R., Gornati, S. V., Hallett, M., Heck, D. H., et al. (2019) · The Cerebellum · doi:10.1007/s12311-019-01041-5 · Cited by 162 · see citing works
The Claustrum Supports Resilience to Distraction
Atlan, G., Terem, A., Peretz‐Rivlin, N., Sehrawat, K., Gonzales, B. J., Pozner, G., Tasaka, G., Goll, Y., Refaeli, R., Zviran, O., et al. (2018) · Current Biology · doi:10.1016/j.cub.2018.06.068 · Cited by 160 · see citing works
Communication in Neural Circuits: Tools, Opportunities, and Challenges
Lerner, T. N., Ye, L., & Deisseroth, K. (2016) · Cell · doi:10.1016/j.cell.2016.02.027 · Cited by 159 · see citing works
Nectow, A. R., & Nestler, E. J. (2020) · Nature reviews. Neuroscience · doi:10.1038/s41583-020-00382-z · Cited by 159 · see citing works
Circuit and molecular architecture of a ventral hippocampal network
Gergues, M. M., Han, K. J., Choi, H. S., Brown, B., Clausing, K. J., Turner, V. S., Vainchtein, I. D., Molofsky, A. V., & Kheirbek, M. A. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0705-8 · Cited by 158 · see citing works
Organization of the inputs and outputs of the mouse superior colliculus
Benavidez, N. L., Bienkowski, M. S., Zhu, M., Garcia, L., Fayzullina, M., Gao, L., Bowman, I., Gou, L., Khanjani, N., Cotter, K. R., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-24241-2 · Cited by 158 · see citing works
Noradrenergic modulation of rhythmic neural activity shapes selective attention
Dahl, M. J., Mather, M., & Werkle‐Bergner, M. (2021) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2021.10.009 · Cited by 158 · see citing works
Rompani, S. B., Müllner, F. E., Wanner, A. A., Zhang, C., Roth, C. N., Yonehara, K., & Roska, B. (2017) · Neuron · doi:10.1016/j.neuron.2017.01.028 · Cited by 156 · see citing works
High-Capacity Adenoviral Vectors: Expanding the Scope of Gene Therapy
Ricobaraza, A., González-Aparicio, M., Mora-Jimenez, L., Lumbreras, S., & Hernández-Alcoceba, R. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103643 · Cited by 155 · see citing works
Basal forebrain volume reliably predicts the cortical spread of Alzheimer’s degeneration
Fernández‐Cabello, S., Kronbichler, M., Dijk, K. R. A. V., Goodman, J. A., Spreng, R. N., Schmitz, T. W., & Initiative, O. B. O. T. A. D. N. (2020) · Brain · doi:10.1093/brain/awaa012 · Cited by 154 · see citing works
The integrated brain network that controls respiration
Krohn, F., Novello, M., van der Giessen, R. S., Zeeuw, C. I. D., Pel, J. J. M., & Bosman, L. W. J. (2023) · eLife · doi:10.7554/elife.83654 · Cited by 155 · see citing works
A Student’s Guide to Neural Circuit Tracing
Saleeba, C., Dempsey, B., Le, S., Goodchild, A., & McMullan, S. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00897 · Cited by 153 · see citing works
Movement and Performance Explain Widespread Cortical Activity in a Visual Detection Task
Salkoff, D. B., Zagha, E., McCarthy, E., & McCormick, D. A. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz206 · Cited by 153 · see citing works
Kim, J., Jung, A.-H., Jeong, D., Choi, I., Kim, K., Shin, S., Kim, S. J., & Lee, S. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4333-15.2016 · Cited by 148 · see citing works
Vagus nerve stimulation induces widespread cortical and behavioral activation
Collins, L. N., Boddington, L. J., Steffan, P. J., & McCormick, D. A. (2021) · Current Biology · doi:10.1016/j.cub.2021.02.049 · Cited by 147 · see citing works
Characterizing and targeting glioblastoma neuron-tumor networks with retrograde tracing
Tetzlaff, S. K., Reyhan, E., Layer, N., Bengtson, C. P., Heuer, A., Schroers, J., Faymonville, A. J., Langeroudi, A. P., Drewa, N., Keifert, E., et al. (2024) · Cell · doi:10.1016/j.cell.2024.11.002 · Cited by 147 · see citing works
Qi, G., Zhang, P., Li, T., Li, M., Zhang, Q., He, F., Zhang, L., Cai, H., Lv, X., Qiao, H., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28190-2 · Cited by 143 · see citing works
Functions and dysfunctions of neocortical inhibitory neuron subtypes
Hattori, R., Kuchibhotla, K. V., Froemke, R. C., & Komiyama, T. (2017) · Nature Neuroscience · doi:10.1038/nn.4619 · Cited by 142 · see citing works
Orexin modulates behavioral fear expression through the locus coeruleus
Soya, S., Takahashi, T. M., McHugh, T. J., Maejima, T., Herlitze, S., Abe, M., Sakimura, K., & Sakurai, T. (2017) · Nature Communications · doi:10.1038/s41467-017-01782-z · Cited by 141 · see citing works
Cholinergic modulation of spatial learning, memory and navigation
Solari, N., & Hangya, B. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14089 · Cited by 139 · see citing works
Connectional architecture of a mouse hypothalamic circuit node controlling social behavior
Lo, L., Yao, S., Kim, D., Cetin, A. H., Harris, J. A., Zeng, H., Anderson, D. J., & Weissbourd, B. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1817503116 · Cited by 138 · see citing works
Self-citationA Hypothalamic Switch for REM and Non-REM Sleep
Chen, K.-S., Xu, M., Zhang, Z., Chang, W.-C., Gaj, T., Schaffer, D. V., & Dan, Y. (2018) · Neuron · doi:10.1016/j.neuron.2018.02.005 · Cited by 137 · see citing works
Locus coeruleus-norepinephrine modulation of sensory processing and perception: A focused review
McBurney-Lin, J., Lu, J., Zuo, Y., & Yang, H. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.06.009 · Cited by 137 · see citing works
Spatiotemporal dynamics of noradrenaline during learned behaviour
Breton‐Provencher, V., Drummond, G. T., Feng, J., Li, Y., & Sur, M. (2022) · Nature · doi:10.1038/s41586-022-04782-2 · Cited by 135 · see citing works
Organization of neural circuits underlying social behavior: A consideration of the medial amygdala
Raam, T., & Hong, W. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.02.008 · Cited by 134 · see citing works
Variance and invariance of neuronal long-term representations
Clopath, C., Bonhoeffer, T., Hübener, M., & Rose, T. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0161 · Cited by 131 · see citing works
Egroo, M. V., Koshmanova, E., Vandewalle, G., & Jacobs, H. I. L. (2022) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2022.101592 · Cited by 132 · see citing works
Genetically identified amygdala–striatal circuits for valence-specific behaviors
Zhang, X., Guan, W., Yang, T., Furlan, A., Xiao, X., Yu, K., An, X., Galbavy, W., Ramakrishnan, C., Deisseroth, K., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00927-0 · Cited by 126 · see citing works
Jordan, R., & Keller, G. B. (2023) · eLife · doi:10.7554/elife.85111 · Cited by 126 · see citing works
Visual intracortical and transthalamic pathways carry distinct information to cortical areas
Blot, A., Roth, M., Gasler, I. T., Javadzadeh, M., Imhof, F., & Hofer, S. B. (2021) · Neuron · doi:10.1016/j.neuron.2021.04.017 · Cited by 122 · see citing works
Monitoring norepinephrine release in vivo using next-generation GRABNE sensors
Feng, J., Dong, H., Lischinsky, J. E., Zhou, J., Deng, F., Zhuang, C., Miao, X., Wang, H., Li, G., Cai, R., et al. (2024) · Neuron · doi:10.1016/j.neuron.2024.03.001 · Cited by 121 · see citing works
Viral Vectors for Neural Circuit Mapping and Recent Advances in Trans-synaptic Anterograde Tracers
Xu, X., Holmes, T. C., Luo, M., Beier, K. T., Horwitz, G. D., Zhao, F., Zeng, W., Hui, M., Semler, B. L., & Sandri-Goldin, R. M. (2020) · Neuron · doi:10.1016/j.neuron.2020.07.010 · Cited by 120 · see citing works
Self-citationDifferential Encoding in Prefrontal Cortex Projection Neuron Classes Across Cognitive Tasks
Lui, J. H., Nguyen, N. D., Grutzner, S. M., Darmanis, S., Peixoto, D., Wagner, M. J., Allen, W. E., Kebschull, J. M., Richman, E. B., Ren, J., et al. (2020) · Cell · doi:10.1016/j.cell.2020.11.046 · Cited by 121 · see citing works
Self-citationA Sensorimotor Pathway via Higher-Order Thalamus
Mo, C., & Sherman, S. M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1467-18.2018 · Cited by 118 · see citing works
Beier, K. T., Gao, X. J., Xie, S. C., DeLoach, K. E., Malenka, R. C., & Luo, L. (2019) · Cell Reports · doi:10.1016/j.celrep.2018.12.040 · Cited by 117 · see citing works
Self-citation5-HT modulation of a medial septal circuit tunes social memory stability
Wu, X., Morishita, W., Beier, K. T., Heifets, B. D., & Malenka, R. C. (2021) · Nature · doi:10.1038/s41586-021-03956-8 · Cited by 116 · see citing works
Self-citationPupil diameter is not an accurate real-time readout of locus coeruleus activity
Megemont, M., McBurney-Lin, J., & Yang, H. (2022) · eLife · doi:10.7554/elife.70510 · Cited by 115 · see citing works
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review