The dual developmental origin of spinal cerebrospinal fluid-contacting neurons gives rise to distinct functional subtypes
Open accessAbstract
Chemical and mechanical cues from the cerebrospinal fluid (CSF) can affect the development and function of the central nervous system (CNS). How such cues are detected and relayed to the CNS remains elusive. Cerebrospinal fluid-contacting neurons (CSF-cNs) situated at the interface between the CSF and the CNS are ideally located to convey such information to local networks. In the spinal cord, these GABAergic neurons expressing the PKD2L1 channel extend an apical extension into the CSF and an ascending axon in the spinal cord. In zebrafish and mouse spinal CSF-cNs originate from two distinct progenitor domains characterized by distinct cascades of transcription factors. Here we ask whether these neurons with different developmental origins differentiate into cells types with different functional properties. We show in zebrafish larva that the expression of specific markers, the morphology of the apical extension and axonal projections, as well as the neuronal targets contacted by CSF-cN axons, distinguish the two CSF-cN subtypes. Altogether our study demonstrates that the developmental origins of spinal CSF-cNs give rise to two distinct functional populations of sensory neurons. This work opens novel avenues to understand how these subtypes may carry distinct functions related to development of the spinal cord, locomotion and posture.
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The adult cell types of Ia inhibitory neurons and CSF-contacting neurons each have dual origins.
“It is already known that the adult cell types of Ia inhibitory neurons and CSF-contacting neurons each have dual origins43,45,121, suggesting that this could be a common occurrence.”
From A harmonized atlas of mouse spinal cord cell types and their spatial organization (2021) · cites this paper as [45]
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1 retracted
Bellipanni, G., Rink, E., & Bally‐Cuif, L. (2002) · Gene Expression Patterns · doi:10.1016/s1567-133x(02)00056-x · Cited by 98 · see citing works
RetractedFiji: an open-source platform for biological-image analysis
Schindelin, J., Arganda-Carreras, I., Frise, E., Kaynig, V., Longair, M., Pietzsch, T., Preibisch, S., Rueden, C., Saalfeld, S., Schmid, B., et al. (2012) · Nature Methods · doi:10.1038/nmeth.2019 · Cited by 66,890 · see citing works
Iliff, J. J., Wang, M., Liao, Y., Plogg, B. A., Peng, W., Gundersen, G. A., Benveniste, H., Vates, G. E., Deane, R., Goldman, S. A., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003748 · Cited by 5,824 · see citing works
Sleep Drives Metabolite Clearance from the Adult Brain
Xie, L., Kang, H., Xu, Q., Chen, M. J., Liao, Y., Thiyagarajan, M., O’Donnell, J., Christensen, D. J., Nicholson, C., Iliff, J. J., et al. (2013) · Science · doi:10.1126/science.1241224 · Cited by 5,411 · see citing works
Globally optimal stitching of tiled 3D microscopic image acquisitions
Preibisch, S., Saalfeld, S., & Tomancak, P. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp184 · Cited by 2,452 · see citing works
Lifeact: a versatile marker to visualize F-actin
Riedl, J., Crevenna, A. H., Kessenbrock, K., Yu, J. H., Neukirchen, D., Bista, M., Bradke, F., Jenne, D., Holak, T. A., Werb, Z., et al. (2008) · Nature Methods · doi:10.1038/nmeth.1220 · Cited by 2,189 · see citing works
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 1,778 · see citing works
Directed evolution of APEX2 for electron microscopy and proximity labeling
Lam, S. S., Martell, J. D., Kamer, K. J., Deerinck, T. J., Ellisman, M. H., Mootha, V. K., & Ting, A. Y. (2014) · Nature Methods · doi:10.1038/nmeth.3179 · Cited by 1,404 · see citing works
Megı́as, M., Emri, Z., Freund, T. F., & Gulyás, A. I. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00496-6 · Cited by 950 · see citing works
Longair, M., Baker, D. A., & Armstrong, J. D. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr390 · Cited by 939 · see citing works
The cells and logic for mammalian sour taste detection
Huang, A. L., Chen, X., Hoon, M. A., Chandrashekar, J. V., Guo, W., Tränkner, D., Ryba, N. J. P., & Zuker, C. S. (2006) · Nature · doi:10.1038/nature05084 · Cited by 814 · see citing works
Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1
Fiala, J. C., Feinberg, M., Popov, V., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08900.1998 · Cited by 758 · see citing works
DeFelipe, J. (1997) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(97)10013-8 · Cited by 550 · see citing works
Transient receptor potential family members PKD1L3 and PKD2L1 form a candidate sour taste receptor
Ishimaru, Y., Inada, H., Kubota, M., Zhuang, H., Tominaga, M., & Matsunami, H. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602702103 · Cited by 497 · see citing works
Low cerebrospinal fluid hypocretin (orexin) and altered energy homeostasis in human narcolepsy
Nishino, S., Ripley, B. A., Overeem, S., Nevšímalová, S., Lammers, G. J., Vaňková, J., Okun, M. L., Rogers, W. M., Brooks, S. N., & Mignot, E. J.-M. (2001) · Annals of Neurology · doi:10.1002/ana.1130 · Cited by 451 · see citing works
Optogenetic dissection of a behavioural module in the vertebrate spinal cord
Wyart, C., Bene, F. D., Warp, E., Scott, E. K., Trauner, D., Baier, H., & Isacoff, E. Y. (2009) · Nature · doi:10.1038/nature08323 · Cited by 409 · see citing works
Self-citationA topographic map of recruitment in spinal cord
McLean, D. L., Fan, J., Higashijima, S.-I., Hale, M. E., & Fetcho, J. R. (2007) · Nature · doi:10.1038/nature05588 · Cited by 384 · see citing works
Flanagan‐Steet, H. R., Fox, M. A., Meyer, D., & Sanes, J. R. (2005) · Development · doi:10.1242/dev.02044 · Cited by 345 · see citing works
Meyer, M. P., & Smith, S. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0223-06.2006 · Cited by 283 · see citing works
The cytoarchitecture of gabaergic neurons in rat spinal cord
Barber, R. P., Vaughn, J. E., & Roberts, E. (1982) · Brain Research · doi:10.1016/0006-8993(82)90107-x · Cited by 255 · see citing works
Kinocilia Mediate Mechanosensitivity in Developing Zebrafish Hair Cells
Kindt, K. S., Finch, G., & Nicolson, T. A. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.05.022 · Cited by 218 · see citing works
A confocal study of spinal interneurons in living larval zebrafish
Hale, M. E., Ritter, D. A., & Fetcho, J. R. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1266 · Cited by 203 · see citing works
Mapping a sensory-motor network onto a structural and functional ground plan in the hindbrain
Koyama, M., Kinkhabwala, A., Satou, C., Higashijima, S.-I., & Fetcho, J. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1012189108 · Cited by 190 · see citing works
Spatial and temporal regulation of ventral spinal cord precursor specification by Hedgehog signaling
Park, H.-C., Shin, J., & Appel, B. (2004) · Development · doi:10.1242/dev.01456 · Cited by 180 · see citing works
Sleep-promoting effects of cerebrospinal fluid from sleep-deprived goats.
Pappenheimer, J. R., Miller, T. B., & Goodrich, C. A. (1967) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.58.2.513 · Cited by 177 · see citing works
CSF-contacting neurons regulate locomotion by relaying mechanical stimuli to spinal circuits
Böhm, U. L., Prendergast, A. E., Djenoune, L., Figueiredo, S. N., Gómez, J., Stokes, C. C. A., Kaiser, S. M., Suster, M. L., Kawakami, K., Charpentier, M., et al. (2016) · Nature Communications · doi:10.1038/ncomms10866 · Cited by 170 · see citing works
Self-citationDelmas, P. (2004) · Cell · doi:10.1016/j.cell.2004.07.007 · Cited by 168 · see citing works
Enhancer trapping in zebrafish using the Sleeping Beauty transposon
Balciunas, D., Davidson, A. E., Sivasubbu, S., Hermanson, S., Welle, Z., & Ekker, S. C. (2004) · BMC Genomics · doi:10.1186/1471-2164-5-62 · Cited by 167 · see citing works
Early appearance of pancreatic hormone-expressing cells in the zebrafish embryo
Argenton, F., Zecchin, E., & Bortolussi, M. (1999) · Mechanisms of Development · doi:10.1016/s0925-4773(99)00151-3 · Cited by 156 · see citing works
Actual problems of the cerebrospinal fluid-contacting neurons
Béla, V. I. G. H., & Vigh‐Teichmann, I. (1998) · Microscopy Research and Technique · doi:10.1002/(sici)1097-0029(19980401)41:1 · Cited by 151 · see citing works
Satou, C., Kimura, Y., & Higashijima, S. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5500-11.2012 · Cited by 150 · see citing works
Über ein zentrales Sinnesorgan (?) bei den Vertebraten
Agduhr, E. (1922) · Brain Structure and Function · doi:10.1007/bf02593586 · Cited by 142 · see citing works
XuvTools: free, fast and reliable stitching of large 3D datasets
Emmenlauer, M., Ronneberger, O., Ponti, A., Schwarb, P., Griffa, A., Filippi, A., Nitschke, R., Driever, W., & BURKHARDT, H. (2009) · Journal of Microscopy · doi:10.1111/j.1365-2818.2008.03094.x · Cited by 142 · see citing works
THE ULTRASTRUCTURE OF THE KINOCILIUM OF THE SENSORY CELLS IN THE INNER EAR AND LATERAL LINE ORGANS
Flock, Å., & Duvall, A. J. (1965) · The Journal of Cell Biology · doi:10.1083/jcb.25.1.1 · Cited by 131 · see citing works
Das „Sagittalorgan“ der Wirbeltiere
Kolmer, W. (1921) · Brain Structure and Function · doi:10.1007/bf02593657 · Cited by 128 · see citing works
Djenoune, L., Khabou, H., Joubert, F., Quan, F. B., Figueiredo, S. N., Bodineau, L., Bene, F. D., Burcklé, C., Tostivint, H., & Wyart, C. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00026 · Cited by 125 · see citing works
Self-citationNeuromodulation of Vertebrate Locomotor Control Networks
Miles, G. B., & Sillar, K. T. (2011) · Physiology · doi:10.1152/physiol.00013.2011 · Cited by 118 · see citing works
The monoamine-containing neurons in the brain of the garfish, Lepisosteus osseus
Parent, A., & Northcutt, R. G. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90132-0 · Cited by 117 · see citing works
Ciliated neurons lining the central canal sense both fluid movement and pH through ASIC3
Jalalvand, E., Robertson, B., Wallén, P., & Grillner, S. E. (2016) · Nature Communications · doi:10.1038/ncomms10002 · Cited by 111 · see citing works
Cerebrodiene: a brain lipid isolated from sleep-deprived cats.
Lerner, R. A., Siuzdak, G. E., Prospero-Garcia, O. E., Henriksen, S. J., Boger, D. L., & Cravatt, B. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.20.9505 · Cited by 110 · see citing works
State-Dependent Modulation of Locomotion by GABAergic Spinal Sensory Neurons
Fidelin, K., Djenoune, L., Stokes, C. C. A., Prendergast, A. E., Gómez, J., Baradel, A., Bene, F. D., & Wyart, C. (2015) · Current Biology · doi:10.1016/j.cub.2015.09.070 · Cited by 108 · see citing works
Self-citationBranchereau, P., Chapron, J., & Meyrand, P. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-07-02598.2002 · Cited by 103 · see citing works
Regulation of the murine TRPP3 channel by voltage, pH, and changes in cell volume
Shimizu, T., Janssens, A., Voets, T., et al. (2008) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-008-0558-6 · Cited by 98 · see citing works
Enigmatic Central Canal Contacting Cells: Immature Neurons in “Standby Mode”?
Marichal, N., García, G., Radmilovich, M., Trujillo-Cenóz, O., & Russo, R. E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6183-08.2009 · Cited by 96 · see citing works
Stoeckel, M. E., Uhl‐Bronner, S., Hugel, S., Veinante, P., Klein, M. J., Mutterer, J., Freund‐Mercier, M. J., & Schlichter, R. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10565 · Cited by 95 · see citing works
Hubbard, J. M., Böhm, U. L., Prendergast, A. E., Tseng, P.-E. B., Newman, M., Stokes, C. C. A., & Wyart, C. (2016) · Current Biology · doi:10.1016/j.cub.2016.08.026 · Cited by 94 · see citing works
Self-citationTeraoka, H., Russell, C. L., Regan, J. C., et al. (2004) · Journal of Neurobiology · doi:10.1002/neu.20023 · Cited by 91 · see citing works
Attenuation of Notch and Hedgehog Signaling Is Required for Fate Specification in the Spinal Cord
Huang, P., Xiong, F., Megason, S. G., & Schier, A. F. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002762 · Cited by 90 · see citing works
The late and dual origin of cerebrospinal fluid-contacting neurons in the mouse spinal cord
Petracca, Y. L., Sartoretti, M. M., Di Bella, D. J., Marin-Burgin, A., Carcagno, A. L., Schinder, A. F., & Lanuza, G. M. (2016) · Development · doi:10.1242/dev.129254 · Cited by 90 · see citing works
New insight into the molecular evolution of the somatostatin family
Tostivint, H., Lihrmann, I., & Vaudry, H. (2008) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2008.02.029 · Cited by 82 · see citing works
Bellipanni, G., Rink, E., & Bally‐Cuif, L. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00119-9 · Cited by 79 · see citing works
Orts-Del’Immagine, A., Wanaverbecq, N., Tardivel, C., Tillement, V., Dallaporta, M., & Trouslard, J. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2012.227959 · Cited by 78 · see citing works
Regulatory interactions specifying Kolmer-Agduhr interneurons
Yang, L., Rastegar, S., & Strähle, U. (2010) · Development · doi:10.1242/dev.048470 · Cited by 77 · see citing works
The Spinal Cord Has an Intrinsic System for the Control of pH
Jalalvand, E., Robertson, B., Tostivint, H., Wallén, P., & Grillner, S. E. (2016) · Current Biology · doi:10.1016/j.cub.2016.03.048 · Cited by 77 · see citing works
Differential expression of two somatostatin genes during zebrafish embryonic development
Devos, N., Deflorian, G., Biemar, F., et al. (2002) · Mechanisms of Development · doi:10.1016/s0925-4773(02)00082-5 · Cited by 73 · see citing works
Quan, F. B., Dubessy, C., Galant, S., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119290 · Cited by 72 · see citing works
Self-citationSternberg, J. R., Severi, K. E., Fidelin, K., Gómez, J., Ihara, H., Alcheikh, Y., Hubbard, J. M., Kawakami, K., Suster, M. L., & Wyart, C. (2016) · Current Biology · doi:10.1016/j.cub.2016.06.037 · Cited by 67 · see citing works
Self-citationChristenson, J., Alford, S. T., Grillner, S., et al. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90516-v · Cited by 65 · see citing works
Béla, V. I. G. H., Vigh‐Teichmann, I., & Aros, B. (1977) · Cell and Tissue Research · doi:10.1007/bf00225666 · Cited by 65 · see citing works
A proton current associated with sour taste: distribution and functional properties
Bushman, J. D., Ye, W., & Liman, E. R. (2015) · The FASEB Journal · doi:10.1096/fj.14-265694 · Cited by 64 · see citing works
Sims, T. J. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730208 · Cited by 62 · see citing works
Orts-Del’Immagine, A., Kästner, A., Tillement, V., Tardivel, C., Trouslard, J., & Wanaverbecq, N. (2014) · PLoS ONE · doi:10.1371/journal.pone.0087748 · Cited by 59 · see citing works
Jalalvand, E., Robertson, B., Wallén, P., Hill, R. H., & Grillner, S. E. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23542 · Cited by 58 · see citing works
Orts-Del’Immagine, A., Seddik, R., Tell, F., Airault, C., Er-Raoui, G., Najimi, M., Trouslard, J., & Wanaverbecq, N. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.07.030 · Cited by 57 · see citing works
Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3
Auer, T. O., Xiao, T., Bercier, V., Gebhardt, C., Duroure, K., Concordet, J., Wyart, C., Suster, M. L., Kawakami, K., Wittbrodt, J., et al. (2015) · eLife · doi:10.7554/elife.05061 · Cited by 50 · see citing works
Self-citationSpinal Cord Injury Enables Aromatic l-Amino Acid Decarboxylase Cells to Synthesize Monoamines
Wienecke, J., Ren, L.-Q., Hultborn, H., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3838-13.2014 · Cited by 48 · see citing works
LaMotte, C. C. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580405 · Cited by 47 · see citing works
Survey of neuropeptide-like immunoreactivity in the lamprey spinal cord
Buchanan, J. T., Brodin, L., Hökfelt, T. G. M., et al. (1987) · Brain Research · doi:10.1016/0006-8993(87)90392-1 · Cited by 44 · see citing works
Roberts, B. L., Maslam, S., Scholten, G., et al. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903540310 · Cited by 44 · see citing works
Parmentier, C., Hameury, E., Dubessy, C., Quan, F. B., Habert, D., Calas, A., Vaudry, H., Lihrmann, I., & Tostivint, H. (2011) · Endocrinology · doi:10.1210/en.2010-1500 · Cited by 42 · see citing works
Self-citationImpact of gene/genome duplications on the evolution of the urotensin II and somatostatin families
Tostivint, H., Quan, F. B., Bougerol, M., et al. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2012.12.015 · Cited by 42 · see citing works
Self-citationBarreiro‐Iglesias, A., Villar‐Cerviño, V., Anadón, R., & Rodicio, M. C. (2008) · The Journal of Comparative Neurology · doi:10.1002/cne.21863 · Cited by 42 · see citing works
England, S. J., Batista, M. F., Mich, J. K., Chen, J., & Lewis, K. E. (2011) · Development · doi:10.1242/dev.066159 · Cited by 40 · see citing works
Christenson, J., Bongianni, F., Grillner, S., et al. (1991) · Brain Research · doi:10.1016/0006-8993(91)90446-3 · Cited by 37 · see citing works
Montgomery, J. E., Wiggin, T. D., Rivera-Pérez, L. M., Lillesaar, C., & Masino, M. A. (2015) · Developmental Neurobiology · doi:10.1002/dneu.22352 · Cited by 36 · see citing works
Colocalization of dopamine and GABA in spinal cord neurones in the sea lamprey
Rodicio, M. C., Villar‐Cerviño, V., Barreiro‐Iglesias, A., et al. (2008) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2007.10.062 · Cited by 32 · see citing works
Structure of the medullo-spinal liquor-contacting neuronal system.
Béla, V. I. G. H., & Vigh‐Teichmann, I. (1971) · PubMed · Cited by 31 · see citing works
Shimosegawa, T., Koizumi, M., Toyota, T., et al. (1986) · Brain Research · doi:10.1016/0006-8993(86)90249-0 · Cited by 27 · see citing works
Megı́as, M., Álvarez‐Otero, R., & Pombal, M. A. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10473 · Cited by 27 · see citing works
Feeding in satiated sheep elicited by intraventricular injections of CSF from fasted sheep
Martin, F. H., Seoane, J. R., & Baile, C. A. (1973) · Life Sciences · doi:10.1016/0024-3205(73)90193-8 · Cited by 26 · see citing works
Chiba, A., & Oka, S. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(98)01011-8 · Cited by 22 · see citing works
Peptidergic neuromodulation of the lumbar locomotor network in the neonatal rat spinal cord
Barrière, G., Bertrand, S. S., & Cazalets, J. (2004) · Peptides · doi:10.1016/j.peptides.2004.09.002 · Cited by 22 · see citing works
Transgenic Zebrafish Recapitulating tbx16 Gene Early Developmental Expression
Wells, S., Nornes, S., & Lardelli, M. T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0021559 · Cited by 22 · see citing works
López, J. M., Moreno, N., Morona, R., et al. (2007) · The Journal of Comparative Neurology · doi:10.1002/cne.21244 · Cited by 17 · see citing works
Jalalvand, E., Robertson, B., Wallén, P., et al. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23584 · Cited by 17 · see citing works
Lovász, L. (1971) · Acta Mathematica Academiae Scientiarum Hungaricae · doi:10.1007/bf01896014 · Cited by 16 · see citing works
Acerbo, M. J., Hellmann, B., & Güntürkün, O. (2003) · Journal of Chemical Neuroanatomy · doi:10.1016/s0891-0618(02)00072-8 · Cited by 15 · see citing works
Yulis, C. R., & Lederis, K. P. (1988) · Cell and Tissue Research · doi:10.1007/bf00226503 · Cited by 14 · see citing works
Allain, A., Ségu, L., Meyrand, P., et al. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2010.05433.x · Cited by 13 · see citing works
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A harmonized atlas of mouse spinal cord cell types and their spatial organization
Russ, D. E., Cross, R. B. P., Li, L., Koch, S. C., Matson, K. J. E., Yadav, A., Alkaslasi, M. R., Lee, D. I., Le Pichon, C. E., Menon, V., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25125-1 · Cited by 255 · see citing works
- Authors
- Djenoune, L., Desban, L., Gomez, J., Sternberg, J. R., Prendergast, A., Langui, D., Quan, F. B., Marnas, H., Auer, T. O., Rio, J.-P., Del Bene, F., Bardet, P.-L., & Wyart, C.
- Affiliations
- Centre National de la Recherche Scientifique (FR)
- Institut Curie (FR)
- Corresponding author
- Bardet, Pierre-Luc
- Wyart, Claire
- ORCID
- Venue
- Scientific Reports
- Published
- 2017-04-07
- Volume
- 7
- Issue
- 1
- Pages
- 719-719
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC5428266
- OpenAlex
- W2604646408
- Cited by
- 65
- References
- 89
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 6 · 2023: 18 · 2022: 7 · 2021: 7 · 2020: 8 · 2019: 5 · 2018: 4 · 2017: 1
- FWCI
- 2.08
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- SERVAL (Université de Lausanne) (publishedVersion, other-oa)
- IRIS (submittedVersion)
- HAL (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Agence Nationale de la Recherche (ANR-10-IAHU-0006)
- Universität zu Köln
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- cerebrospinal fluid-contacting neurons, spinal cord, developmental origins, GABAergic neurons, sensory neurons, axonal projections, zebrafish, mice, transcription factor cascade, locomotion, posture
- MeSH terms
- Animals, Axons, Carrier Proteins, Cell Differentiation, Cerebrospinal Fluid, Fluorescent Antibody Technique, Ganglia, Spinal, Homozygote, Mutation, Neurons, Sensory Receptor Cells, Spinal Cord, Spinal Nerve Roots, Zebrafish, Signal Transduction, Biomarkers, Zebrafish Proteins, Animals, Genetically Modified, TRPP Cation Channels
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 ›
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