A population code for spatial representation in the zebrafish telencephalon.


Journal

Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462

Informations de publication

Date de publication:
28 Aug 2024
Historique:
received: 24 10 2022
accepted: 23 07 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 28 8 2024
Statut: aheadofprint

Résumé

Spatial learning in teleost fish requires an intact telencephalon

Identifiants

pubmed: 39198641
doi: 10.1038/s41586-024-07867-2
pii: 10.1038/s41586-024-07867-2
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

Références

Rodríguez, F. et al. Spatial cognition in teleost fish: strategies and mechanisms. Animals (Basel) 11, 2271 (2021).
pubmed: 34438729 doi: 10.3390/ani11082271
Briscoe, S. D. & Ragsdale, C. W. Evolution of the chordate telencephalon. Curr. Biol. 29, R647–R662 (2019).
pubmed: 31287987 pmcid: 11073819 doi: 10.1016/j.cub.2019.05.026
Pandey, S., Moyer, A. J. & Thyme, S. B. A single-cell transcriptome atlas of the maturing zebrafish telencephalon. Genome Res. 33, 658–671 (2023).
pubmed: 37072188 pmcid: 10234298 doi: 10.1101/gr.277278.122
Tanimoto, Y. et al. Transgenic tools targeting the basal ganglia reveal both evolutionary conservation and specialization of neural circuits in zebrafish. Cell Rep. 43, 113916 (2024).
pubmed: 38484735 doi: 10.1016/j.celrep.2024.113916
O’Keefe, J. & Dostrovsky, J. The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. Brain Res. 34, 171–175 (1971).
pubmed: 5124915 doi: 10.1016/0006-8993(71)90358-1
O’Keefe, J. & Nadel, L. The Hippocampus as a Cognitive Map (Oxford Univ. Press, 1978).
Kim, D. H. et al. Pan-neuronal calcium imaging with cellular resolution in freely swimming zebrafish. Nat. Methods 14, 1107–1114 (2017).
pubmed: 28892088 doi: 10.1038/nmeth.4429
Skaggs, W. E., Mcnaughton, B. L., Gothard, K. M. & Markus, E. J. Information theoretic approach to deciphering the hippocampal code. In Advances in Neural Information Processing System 5 (eds. Hanson, S. J., Cowan, J. D. & Giles, C. J.) 1030–1037 (Morgan Kaufmann, 1993) .
O’ Keefe, J. & Burgess, N. Geometric determinants of the place fields of hippocampal neurons. Nature 381, 425–428 (1996).
pubmed: 8632799 doi: 10.1038/381425a0
Muller, R. U. & Kubie, J. L. The effects of changes in the environment on the spatial firing of hippocampal complex-spike cells. J. Neurosci. 7, 1951–1968 (1987).
pubmed: 3612226 pmcid: 6568940 doi: 10.1523/JNEUROSCI.07-07-01951.1987
Chen, G., King, J. A., Burgess, N. & O’Keefe, J. How vision and movement combine in the hippocampal place code. Proc. Natl Acad. Sci. USA 110, 378–383 (2013).
pubmed: 23256159 doi: 10.1073/pnas.1215834110
Cheng, K. A purely geometric module in the rat’s spatial representation. Cognition 23, 149–178 (1986).
pubmed: 3742991 doi: 10.1016/0010-0277(86)90041-7
Savelli, F. & Knierim, J. J. Origin and role of path integration in the cognitive representations of the hippocampus: computational insights into open questions. J. Exp. Biol. 222, jeb188912 (2019).
pubmed: 30728236 pmcid: 7375830 doi: 10.1242/jeb.188912
McNaughton, B. L., Battaglia, F. P., Jensen, O., Moser, E. I. & Moser, M. B. Path integration and the neural basis of the ‘cognitive map’. Nat. Rev. Neurosci. 7, 663–678 (2006).
pubmed: 16858394 doi: 10.1038/nrn1932
Lee, S. A., Vallortigara, G., Flore, M., Spelke, E. S. & Sovrano, V. A. Navigation by environmental geometry: the use of zebrafish as a model. J. Exp. Biol. 216, 3693 (2013).
pubmed: 23788708 pmcid: 4236227
Payne, H. L., Lynch, G. F. & Aronov, D. Neural representations of space in the hippocampus of a food-caching bird. Science 373, 343–348 (2021).
pubmed: 34437154 pmcid: 8503942 doi: 10.1126/science.abg2009
Ulanovsky, N. & Moss, C. F. Hippocampal cellular and network activity in freely moving echolocating bats. Nat. Neurosci. 10, 224–233 (2007).
pubmed: 17220886 doi: 10.1038/nn1829
Kumar, S. & Hedges, S. B. A molecular timescale for vertebrate evolution. Nature 392, 917–920 (1998).
pubmed: 9582070 doi: 10.1038/31927
Nieuwenhuys, R. The forebrain of Actinopterygians revisited. Brain Behav. Evol. 73, 229–252 (2009).
pubmed: 19546532 doi: 10.1159/000225622
Cohen, L., Vinepinsky, E., Donchin, O. & Segev, R. Boundary vector cells in the goldfish central telencephalon encode spatial information. PLoS Biol. 21, e3001747 (2023).
pubmed: 37097992 pmcid: 10128963 doi: 10.1371/journal.pbio.3001747
Vinepinsky, E. et al. Representation of edges, head direction, and swimming kinematics in the brain of freely-navigating fish. Sci. Rep. 10, 14762 (2020).
pubmed: 32901058 pmcid: 7479115 doi: 10.1038/s41598-020-71217-1
Canfield, J. G. & Mizumori, S. J. Y. Methods for chronic neural recording in the telencephalon of freely behaving fish. J. Neurosci. Methods 133, 127–134 (2004).
pubmed: 14757353 doi: 10.1016/j.jneumeth.2003.10.011
Fotowat, H., Lee, C., Jun, J. J. & Maler, L. Neural activity in a hippocampus-like region of the teleost pallium is associated with active sensing and navigation. eLife 8, e44119 (2019).
pubmed: 30942169 pmcid: 6469930 doi: 10.7554/eLife.44119
Ahrens, M. B., Orger, M. B., Robson, D. N., Li, J. M. & Keller, P. J. Whole-brain functional imaging at cellular resolution using light-sheet microscopy. Nat. Methods 10, 413–420 (2013).
pubmed: 23524393 doi: 10.1038/nmeth.2434
Ahrens, M. B. et al. Brain-wide neuronal dynamics during motor adaptation in zebrafish. Nature 485, 471–477 (2012).
pubmed: 22622571 pmcid: 3618960 doi: 10.1038/nature11057
McNaughton, B. L., Barnes, C. A. & O’Keefe, J. The contributions of position, direction, and velocity to single unit activity in the hippocampus of freely-moving rats. Exp. Brain Res. 52, 41–49 (1983).
pubmed: 6628596 doi: 10.1007/BF00237147
Marques, J. C., Li, M., Schaak, D., Robson, D. N. & Li, J. M. Internal state dynamics shape brainwide activity and foraging behaviour. Nature 577, 239–243 (2020).
pubmed: 31853063 doi: 10.1038/s41586-019-1858-z
Petrucco, L. et al. Neural dynamics and architecture of the heading direction circuit in a vertebrate brain. Nat. Neurosci. 26, 765–773 (2023).
Severi, K. E. et al. Neural control and modulation of swimming speed in the larval zebrafish. Neuron 83, 692–707 (2014).
pubmed: 25066084 pmcid: 4126853 doi: 10.1016/j.neuron.2014.06.032
Huszár, R., Zhang, Y., Blockus, H. & Buzsáki, G. Preconfigured dynamics in the hippocampus are guided by embryonic birthdate and rate of neurogenesis. Nat. Neurosci. 25, 1201–1212 (2022).
pubmed: 35995878 pmcid: 10807234 doi: 10.1038/s41593-022-01138-x
Kinsky, N. R., Sullivan, D. W., Mau, W., Hasselmo, M. E. & Eichenbaum, H. B. Hippocampal place fields maintain a coherent and flexible map across long timescales. Curr. Biol. 28, 3578–3588 (2018).
pubmed: 30393037 pmcid: 6331214 doi: 10.1016/j.cub.2018.09.037
Friedrich, J. et al. Fast constrained non-negative matrix factorization for whole-brain calcium imaging data. http://www.stat.columbia.edu/~johannes/docs/nips2015.pdf (2015).
Lever, C., Burton, S., Jeewajee, A., O’Keefe, J. & Burgess, N. Boundary vector cells in the subiculum of the hippocampal formation. J. Neurosci. 29, 9771–9777 (2009).
pubmed: 19657030 pmcid: 2736390 doi: 10.1523/JNEUROSCI.1319-09.2009
Barry, C. et al. The boundary vector cell model of place cell firing and spatial memory. Rev. Neurosci. 17, 71–97 (2006).
pubmed: 16703944 pmcid: 2677716 doi: 10.1515/REVNEURO.2006.17.1-2.71
Solstad, T., Boccara, C. N., Kropff, E., Moser, M. B. & Moser, E. I. Representation of geometric borders in the entorhinal cortex. Science 322, 1865–1868 (2008).
pubmed: 19095945 doi: 10.1126/science.1166466
Zhang, K., Ginzburg, I., McNaughton, B. L. & Sejnowski, T. J. Interpreting neuronal population activity by reconstruction: unified framework with application to hippocampal place cells. J. Neurophysiol. 79, 1017–1044 (1998).
pubmed: 9463459 doi: 10.1152/jn.1998.79.2.1017
Tenenbaum, J. B., De Silva, V. & Langford, J. C. A global geometric framework for nonlinear dimensionality reduction. Science 290, 2319–2323 (2000).
pubmed: 11125149 doi: 10.1126/science.290.5500.2319
Lever, C., Wills, T., Cacucci, F., Burgess, N. & O’Keefe, J. Long-term plasticity in hippocampal place-cell representation of environmental geometry. Nature 416, 90–94 (2002).
pubmed: 11882899 doi: 10.1038/416090a
Knierim, J. J., Kudrimoti, H. S. & McNaughton, B. L. Place cells, head direction cells, and the learning of landmark stability. J. Neurosci. 15, 1648–1659 (1995).
pubmed: 7891125 pmcid: 6578145 doi: 10.1523/JNEUROSCI.15-03-01648.1995
Sanders, H., Wilson, M. A. & Gershman, S. J. Hippocampal remapping as hidden state inference. eLife 9, e51140 (2020).
pubmed: 32515352 pmcid: 7282808 doi: 10.7554/eLife.51140
Alme, C. B. et al. Place cells in the hippocampus: eleven maps for eleven rooms. Proc. Natl Acad. Sci. USA 111, 18428–18435 (2014).
pubmed: 25489089 pmcid: 4284589 doi: 10.1073/pnas.1421056111
Fyhn, M., Hafting, T., Treves, A., Moser, M. B. & Moser, E. I. Hippocampal remapping and grid realignment in entorhinal cortex. Nature 446, 190–194 (2007).
pubmed: 17322902 doi: 10.1038/nature05601
Yoganarasimha, D., Yu, X. & Knierim, J. J. Head direction cell representations maintain internal coherence during conflicting proximal and distal cue rotations: comparison with hippocampal place cells. J. Neurosci. 26, 622–631 (2006).
doi: 10.1523/JNEUROSCI.3885-05.2006
Muessig, L. et al. Environment geometry alters subiculum boundary vector cell receptive fields in adulthood and early development. Nat. Commun. 15, 982 (2024).
pubmed: 38302455 pmcid: 10834499 doi: 10.1038/s41467-024-45098-1
Sharif, F., Tayebi, B., Buzsáki, G., Royer, S. & Fernandez-Ruiz, A. Subcircuits of deep and superficial CA1 place cells support efficient spatial coding across heterogeneous environments. Neuron 109, 363–376 (2021).
pubmed: 33217328 doi: 10.1016/j.neuron.2020.10.034
Tan, H. M., Wills, T. J. & Cacucci, F. The development of spatial and memory circuits in the rat. Wiley Interdiscip. Rev. Cogn. Sci. 8, e1424 (2017).
doi: 10.1002/wcs.1424
Wills, T. J., Cacucci, F., Burgess, N. & O’Keefe, J. Development of the hippocampal cognitive map in preweanling rats. Science 328, 1573–1576 (2010).
pubmed: 20558720 pmcid: 3543985 doi: 10.1126/science.1188224
Skaggs, W. E. & McNaughton, B. L. Spatial firing properties of hippocampal CA1 populations in an environment containing two visually identical regions. J. Neurosci. 18, 8455–8466 (1998).
pubmed: 9763488 pmcid: 6792855 doi: 10.1523/JNEUROSCI.18-20-08455.1998
Grieves, R. M., Jenkins, B. W., Harland, B. C., Wood, E. R. & Dudchenko, P. A. Place field repetition and spatial learning in a multicompartment environment. Hippocampus 26, 118–134 (2016).
pubmed: 26190393 doi: 10.1002/hipo.22496
Spiers, H. J., Hayman, R. M. A., Jovalekic, A., Marozzi, E. & Jeffery, K. J. Place field repetition and purely local remapping in a multicompartment environment. Cereb. Cortex 25, 10–25 (2015).
pubmed: 23945240 doi: 10.1093/cercor/bht198
Rohlfing, T. & Maurer, C. R. Nonrigid image registration in shared-memory multiprocessor environments with application to brains, breasts, and bees. IEEE Trans. Inf. Technol. Biomed. 7, 16–25 (2003).
pubmed: 12670015 doi: 10.1109/TITB.2003.808506
Randlett, O. et al. Whole-brain activity mapping onto a zebrafish brain atlas. Nat. Methods 1039–1046 (2015).
Gauthier, J. L. & Tank, D. W. A dedicated population for reward coding in the hippocampus. Neuron 99, 179–193 (2018).
pubmed: 30008297 pmcid: 7023678 doi: 10.1016/j.neuron.2018.06.008
Chen, T.-W. et al. Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature 499, 295–300 (2013).
pubmed: 23868258 pmcid: 3777791 doi: 10.1038/nature12354
Pedregosa Fabian, et al. Scikit-learn: machine learning in Python. J. Mach. Learn. Res. 12, 2825–2830 (2011).
Vinepinsky, E., Perchik, S. & Segev, R. A generalized linear model of a navigation network. Front. Neural Circuits 14, 56 (2020).
pubmed: 33013326 pmcid: 7509173 doi: 10.3389/fncir.2020.00056
Bezanson, J., Edelman, A., Karpinski, S. & Shah, V. B. Julia: a fresh approach to numerical computing. SIAM Rev. Soc. Ind. Appl. Math. 59, 65–98 (2017).
Besard, T., Foket, C. & De Sutter, B. Effective extensible programming: unleashing Julia on GPUs. IEEE Trans. Parallel Distrib. Syst. 30, 827–841 (2019).
doi: 10.1109/TPDS.2018.2872064

Auteurs

Chuyu Yang (C)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany.
University of Tuebingen, Tuebingen, Germany.

Lorenz Mammen (L)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany.
University of Tuebingen, Tuebingen, Germany.
Department of Neurobiology and Behavior, Cornell University, Ithaca, NY, USA.

Byoungsoo Kim (B)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany.
University of Tuebingen, Tuebingen, Germany.

Meng Li (M)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany.

Drew N Robson (DN)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany. drew.robson@tuebingen.mpg.de.

Jennifer M Li (JM)

Max Planck Institute for Biological Cybernetics, Tuebingen, Germany. jennifer.li@tuebingen.mpg.de.

Classifications MeSH