The DOI matches its Crossref record; 76 of the 77 references it cites were found in a registry or an index.
Semaphorin 3F Is a Bifunctional Guidance Cue for Dopaminergic Axons and Controls Their Fasciculation, Channeling, Rostral Growth, and Intracortical Targeting
Open accessAbstract
Dopaminergic neurons in the mesodiencephalon (mdDA neurons) make precise synaptic connections with targets in the forebrain via the mesostriatal, mesolimbic, and mesoprefrontal pathways. Because of the functional importance of these remarkably complex ascending axon pathways and their implication in human disease, the mechanisms underlying the development of these connections are of considerable interest. Despite extensive in vitro studies, the molecular determinants that ensure the perfect formation of these pathways in vivo remain mostly unknown. Here, we determine the embryonic origin and ontogeny of the mouse mesoprefrontal pathway and use these data to reveal an unexpected requirement for semaphorin 3F (Sema3F) and its receptor neuropilin-2 (Npn-2) during mdDA pathway development using tissue culture approaches and analysis of sema3F−/−,npn-2−/−, and npn-2−/−;TH-Cre mice. We show that Sema3F is a bifunctional guidance cue for mdDA axons, some of which have the remarkable ability to regulate their responsiveness to Sema3F as they develop. During early developmental stages, Sema3F chemorepulsion controls previously uncharacterized aspects of mdDA pathway development through both Npn-2-dependent (axon fasciculation and channeling) and Npn-2-independent (rostral growth) mechanisms. Later on, chemoattraction mediated by Sema3F and Npn-2 is required to orient mdDA axon projections in the cortical plate of the medial prefrontal cortex. This latter finding demonstrates that regulation of axon orientation in the target field occurs by chemoattractive mechanisms, and this is likely to also apply to other neural systems. In all, this study provides a framework for additional dissection of the molecular basis of mdDA pathway development and disease.
Overview
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
Verification
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“A subset of the medial part of the ventral tegmental area (VTA) starts to project to prefrontal subdomains around E15/E16 (rodent) and week 10–13 in human [155–158].”
From Development of prefrontal cortex (2022) · cites this paper as [156]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“while Semaphorin3F is orchestrating their fasciculation, rostral growth and targeting within the various mPFC subdomains [156].”
From Development of prefrontal cortex (2022) · cites this paper as [156]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The Molecular Biology of Axon Guidance
Tessier‐Lavigne, M., & Goodman, C. S. (1996) · Science · doi:10.1126/science.274.5290.1123 · Cited by 3,311
Dopamine neuron systems in the brain: An update
Björklund, A., & Dunnett, S. B. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.006 · Cited by 1,777
Swanson, L. W. (1982) · Brain Research Bulletin · doi:10.1016/0361-9230(82)90145-9 · Cited by 1,718 · cited 1×
“In the adult mouse, mesoprefrontal mdDA projections originate in the medial VTA (Fallon, 1981; Swanson, 1982; Margolis et al., 2006; Lammel et al., 2008).”
BackgroundIkemoto, S. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.05.004 · Cited by 1,477
Neuropilin is a semaphorin III receptor.
Kolodkin, A., Levengood, D. V., Rowe, E. G., Tai, Y.-T., Giger, R., & Ginty, D. (1997) · Cell · doi:10.1016/s0092-8674(00)80535-8 · Cited by 1,262
Self-citationGong, 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
Unique properties of mesoprefrontal neurons within a dual mesocorticolimbic dopamine system
Lammel, S., Hetzel, A., Häckel, O., Jones, I., Liss, B., & Roeper, J. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.022 · Cited by 976
Tbr1 regulates differentiation of the preplate and layer 6
Hevner, R. F., Shi, L., Justice, N., Hsueh, Y.-P., Sheng, M., Smiga, S., Bulfone, A., Goffinet, A. M., Campagnoni, A. T., & Rubenstein, J. L. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00211-2 · Cited by 857
Conversion of Neuronal Growth Cone Responses from Repulsion to Attraction by Cyclic Nucleotides
Song, H., Ming, G., He, Z., Lehmann, M., McKerracher, L. J., Tessier‐Lavigne, M., & Poo, M.-M. (1998) · Science · doi:10.1126/science.281.5382.1515 · Cited by 796
Molecular Mechanisms of Axon Guidance
Dickson, B. J. (2002) · Science · doi:10.1126/science.1072165 · Cited by 721
Cited by
Sorted by citations
Development of prefrontal cortex
Kolk, S. M., & Rakic, P. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-021-01137-9 · Cited by 378
“Steering dopaminergic projections from the VTA via the medial forebrain bundle toward forebrain regions mostly depend on a coordinated action of the guidance molecules Dcc and Netrin-1 mediated by microRNA miR-218 control of Dcc expression in the VTA [159–161], while Semaphorin3F is orchestrating their fasciculation,…”
BackgroundSelf-citationC 9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits
Koppers, M., Blokhuis, A. M., Westeneng, H., Terpstra, M. L., Zundel, C. A. C., de Sá, R. V., Schellevis, R. D., Waite, A. J., Blake, D. J., Veldink, J. H., et al. (2015) · Annals of Neurology · doi:10.1002/ana.24453 · Cited by 301
Self-citationGetting neural circuits into shape with semaphorins
Pasterkamp, R. J. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3302 · Cited by 281
Self-citationMidbrain dopaminergic neurons: A review of the molecular circuitry that regulates their development
Hegarty, S. V., Sullivan, A. M., & O’Keeffe, G. W. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.04.014 · Cited by 190
Fenstermaker, A. G., Prasad, A. A., Bechara, A., Adolfs, Y., Tissir, F., Goffinet, A. M., Zou, Y., & Pasterkamp, R. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4508-10.2010 · Cited by 162
Self-citationSchubert, D., Martens, G. J. M., & Kolk, S. M. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.147 · Cited by 157
Self-citationWiring the Brain: The Biology of Neuronal GuidancePreprint
Chédotal, A., & Richards, L. J. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001917 · Cited by 158
Wu, C., Zhu, J., Wager‐Miller, J., Wang, S., O’Leary, D. D. M., Monory, K., Lutz, B., Mackie, K., & Lu, H. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07337.x · Cited by 143
Mesocorticolimbic Dopamine Pathways Across Adolescence: Diversity in Development
Reynolds, L. M., & Flores, C. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.735625 · Cited by 137
Semaphorins in Adult Nervous System Plasticity and Disease
Carulli, D., de Winter, F., & Verhaagen, J. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672891 · Cited by 137
Reynolds, L. M., Pokinko, M., Torres-Berrío, A., Cuesta, S., Lambert, L. C., Del Cid Pellitero, E., Wodzinski, M., Manitt, C., Krimpenfort, P., Kolb, B., et al. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.06.009 · Cited by 129
Development, wiring and function of dopamine neuron subtypes
Garritsen, O., van Battum, E. Y., Grossouw, L. M., & Pasterkamp, R. J. (2023) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00669-3 · Cited by 128
Self-citationWitteveen, J. S., Willemsen, M. H., Dombroski, T. C. D., van Bakel, N. H. M., Nillesen, W. M., van Hulten, J. A., Jansen, E. J. R., Verkaik, D., Veenstra-Knol, H. E., van Ravenswaaij-Arts, C. M. A., et al. (2016) · Nature Genetics · doi:10.1038/ng.3619 · Cited by 128
Self-citationWnt5a Regulates Midbrain Dopaminergic Axon Growth and Guidance
Blakely, B. D., Bye, C. R., Fernando, C. V., Horne, M. K., Macheda, M. L., Stacker, S. A., Arenas, E., & Parish, C. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018373 · Cited by 100
Immunohistochemical distribution of PlexinA4 in the adult rat central nervous system
Gutekunst (2010) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2010.00025 · Cited by 99
Molecular mechanisms of dendrite morphogenesis
Arikkath, J. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00061 · Cited by 113
Receptor complexes for each of the Class 3 Semaphorins
Sharma, A., Verhaagen, J., & Harvey, A. R. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00028 · Cited by 93
Semaphorin Signaling in Vertebrate Neural Circuit Assembly
Yoshida, Y. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00071 · Cited by 85
Cxcl12/Cxcr4 signaling controls the migration and process orientation of A9-A10 dopaminergic neurons
Yang, S., Edman, L. C., Sánchez‐Alcañiz, J. A., Fritz, N., Bonilla, S., Hecht, J. H., Uhlén, P., Pleasure, S. J., Villaescusa, C., Marín, Ó., et al. (2013) · Development · doi:10.1242/dev.098145 · Cited by 83
Niederkofler, V., Asher, T. E., & Dymecki, S. M. (2015) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5b00021 · Cited by 75
van Battum, E. Y., Gunput, R. F., Lemstra, S., Groen, E. J. N., Yu, K. L., Adolfs, Y., Zhou, Y., Hoogenraad, C. C., Yoshida, Y., Schachner, M., et al. (2014) · Nature Communications · doi:10.1038/ncomms5317 · Cited by 76
Self-citationTcf4 is required for correct brain development during embryogenesis
Mesman, S., Bakker, R., & Smidt, M. P. (2020) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2020.103502 · Cited by 71
Self-citationNeuroprotection and neurorestoration as experimental therapeutics for Parkinson's disease
Francardo, V., Schmitz, Y., Sulzer, D. L., & Cenci, M. A. (2017) · Experimental Neurology · doi:10.1016/j.expneurol.2017.10.001 · Cited by 66
Demyanenko, G. P., Riday, T. T., Tran, T. S., Dalal, J. S., Darnell, E. P., Brennaman, L. H., Sakurai, T., Grumet, M., Philpot, B. D., & Maness, P. F. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4467-10.2011 · Cited by 63
Self-citationMICAL-1 Is a Negative Regulator of MST-NDR Kinase Signaling and Apoptosis
Zhou, Y., Adolfs, Y., Pijnappel, W. W. M. P., Fuller, S. J., van der Schors, R. C., Li, K. W., Sugden, P. H., Smit, A. B., Hergovich, A., & Pasterkamp, R. J. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01389-10 · Cited by 64
Self-citationMidbrain dopaminergic axons are guided longitudinally through the diencephalon by Slit/Robo signals
Dugan, J. P., Stratton, A., Riley, H. P., Farmer, W. T., & Mastick, G. S. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.11.003 · Cited by 60
Kotan, L. D., Ternier, G., Çakır, A. D., Emeksiz, H. C., Turan, İ., Delpouve, G., Kardelen, A. R. D., Özcabı, B., Işık, E., Mengen, E., et al. (2021) · Genetics in Medicine · doi:10.1038/s41436-020-01087-5 · Cited by 56
Witteveen, J. S., Middelman, A., van Hulten, J. A., Martens, G. J. M., Homberg, J. R., & Kolk, S. M. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00143 · Cited by 53
Self-citationSemaphorin signaling: molecular switches at the midline
Derijck, A. A. H. A., van Erp, S., & Pasterkamp, R. J. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.06.007 · Cited by 57
Self-citationSchmidt, E. R. E., Brignani, S., Adolfs, Y., Lemstra, S., Demmers, J., Vidaki, M., Donahoo, A.-L. S., Lilleväli, K., Vasar, E., Richards, L. J., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.036 · Cited by 55
Self-citationVGluT2 Expression in Dopamine Neurons Contributes to Postlesional Striatal Reinnervation
Kouwenhoven, W. M., Fortin, G., Penttinen, A., Florence, C., Delignat‐Lavaud, B., Bourque, M.-J., Trimbuch, T., Luppi, M. P., Salvail-Lacoste, A., Legault, P., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0823-20.2020 · Cited by 55
The Development of the Mesoprefrontal Dopaminergic System in Health and Disease
Islam, K. U. S., Meli, N., & Blaess, S. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.746582 · Cited by 55
Establishing diversity in the dopaminergic system
Bodea, G. O., & Blaess, S. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.09.016 · Cited by 50
Canonical BMP–Smad Signalling Promotes Neurite Growth in Rat Midbrain Dopaminergic Neurons
Hegarty, S. V., Collins, L., Gavin, A. M., Roche, S. L., Wyatt, S. L., Sullivan, A. M., & O’Keeffe, G. W. (2014) · NeuroMolecular Medicine · doi:10.1007/s12017-014-8299-5 · Cited by 48
Brignani, S., & Pasterkamp, R. J. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00055 · Cited by 47
Self-citationBrignani, S., Raj, D. D. A., Schmidt, E. R. E., Düdükcü, Ö., Adolfs, Y., Ruiter, A. A. D., Rybiczka-Tešulov, M., Verhagen, M. G., van der Meer, C., Broekhoven, M. H., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.05.037 · Cited by 46
Self-citationDopaminergic axon guidance: which makes what?
Prestoz, L., Jaber, M., & Gaillard, A. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00032 · Cited by 43
Chakrabarty, K., von Oerthel, L., Hellemons, A. J. C. G. M., Clotman, F., Espana, A., Koerkamp, M. J. A. G., Holstege, F. C. P., Pasterkamp, R. J., & Smidt, M. P. (2012) · Biology Open · doi:10.1242/bio.20121230 · Cited by 41
Self-citationBye, C. R., Rytova, V., Alsanie, W. F., Parish, C. L., & Thompson, L. H. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.0278-19.2019 · Cited by 40
Mesman, S., & Smidt, M. P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00353 · Cited by 38
Self-citationIntegration of Opposing Semaphorin Guidance Cues in Cortical Axons
Rüdiger, T., Zimmer‐Bensch, G., Barchmann, S., Castellani, V., Bagnard, D., & Bolz, J. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs044 · Cited by 38
Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
Meyer, L. A. T., Fritz, J., Pierdant, M., & Bagnard, D. (2016) · Cell Adhesion & Migration · doi:10.1080/19336918.2016.1261785 · Cited by 37
Georgieff, M., Tran, P. V., & Carlson, E. S. (2018) · Development and Psychopathology · doi:10.1017/s0954579418000500 · Cited by 43
Ceci, C., Lacal, P. M., Barbaccia, M. L., Mercuri, N. B., Graziani, G., & Ledonne, A. (2024) · Pharmacological Research · doi:10.1016/j.phrs.2024.107101 · Cited by 36
Development of Posterior Hypothalamic Neurons Enlightens a Switch in the Prosencephalic Basic Plan
Croizier, S., Amiot, C., Chen, X., Presse, F., Nahon, J., Wu, J. Y., FELLMANN, D., & Risold, P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028574 · Cited by 39
Torre, E. R., Gutekunst, C., & Gross, R. E. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.03.003 · Cited by 35
Li, Z., Jagadapillai, R., Gozal, E., & Barnes, G. N. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1450-9 · Cited by 34
Chauvet, S., Burk, K., & Mann, F. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1278-4 · Cited by 40
Paul, E. J., Tossell, K., & Ungless, M. A. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14534 · Cited by 33
The transcription factor BCL11A defines distinct subsets of midbrain dopaminergic neurons
Tolve, M., Ulusoy, A., Patikas, N., Islam, K. U. S., Bodea, G. O., Öztürk, E., Broske, B., Mentani, A., Wagener, A., van Loo, K. M. J., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109697 · Cited by 33
Fibroblast growth factor 2 regulates adequate nigrostriatal pathway formation in mice
Baron, O., Ratzka, A., & Grothe, C. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23138 · Cited by 34
Amphetamine disrupts dopamine axon growth in adolescence by a sex-specific mechanism in mice
Reynolds, L. M., Hernandez, G., MacGowan, D., Popescu, C., Nouel, D., Cuesta, S., Burke, S., Savell, K. E., Zhao, J., Restrepo-Lozano, J. M., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39665-1 · Cited by 30
Jajodia, A., Kaur, H., Kumari, K., Gupta, M., Baghel, R., Srivastava, A., Sood, M., Chadda, R. K., Jain, S., & Kukreti, R. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.031 · Cited by 31
Blakely, B. D., Bye, C. R., Fernando, C. V., Prasad, A. A., Pasterkamp, R. J., Macheda, M. L., Stacker, S. A., & Parish, C. L. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0066 · Cited by 31
Self-citationWitteveen, J. S., Loopstok, S. R., Luque-Ballesteros, L., Boonstra, A., van Bakel, N. H. M., Boekel, W. V., Martens, G. J. M., Visser, J. E., & Kolk, S. M. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04326-x · Cited by 29
Self-citationGarcia, L. P., Witteveen, J. S., Middelman, A., van Hulten, J. A., Martens, G. J. M., Homberg, J. R., & Kolk, S. M. (2019) · Molecular Neurobiology · doi:10.1007/s12035-018-1105-x · Cited by 28
Self-citationFrizzled3 Controls Axonal Polarity and Intermediate Target Entry during Striatal Pathway Development
Morello, F., Prasad, A. A., Rehberg, K., de Sá, R. V., Antón-Bolaños, N., Leyva‐Díaz, E., Adolfs, Y., Tissir, F., López‐Bendito, G., & Pasterkamp, R. J. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1840-15.2015 · Cited by 28
Self-citationSgadó, P., Ferretti, E., Grbec, D., Bozzi, Y., & Simon, H. H. (2012) · Neural Development · doi:10.1186/1749-8104-7-24 · Cited by 28
Komada, M., Iguchi, T., Takeda, T., Ishibashi, M., & Sato, M. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.05.006 · Cited by 27
van den Heuvel, D. M. A., Hellemons, A. J. C. G. M., & Pasterkamp, R. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055828 · Cited by 27
Self-citationMesman, S., von Oerthel, L., & Smidt, M. P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097926 · Cited by 27
Self-citationDíaz-Martínez, N. E., Tamaríz, E., Díaz, N. F., García‐Peña, C. M., Varela‐Echavarría, A., & Velasco, I. (2013) · Molecular Therapy · doi:10.1038/mt.2013.78 · Cited by 27
Yuan, H., Yang, M., Han, X., & Ni, X. (2018) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2018/3052058 · Cited by 25
Lindholm, T., Risling, M., Carlstedt, T. P., Hammarberg, H., Wallquist, W., Cullheim, S., & Sköld, M. K. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00049 · Cited by 25
Hernández-Enríquez, B., Wu, Z., Martinez, E., Olsen, O., Kaprielian, Z., Maness, P. F., Yoshida, Y., Tessier‐Lavigne, M., & Tran, T. S. (2015) · Genes & Development · doi:10.1101/gad.268086.115 · Cited by 28
Self-citationGuidance of longitudinally projecting axons in the developing central nervous system
Sakai, N., & Kaprielian, Z. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00059 · Cited by 22
Cord, B. J., Li, J., Works, M. G., McConnell, S. K., Palmer, T. D., & Hynes, M. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.07.004 · Cited by 21
Kroeze, Y., Oti, M., van Beusekom, E., Cooijmans, R. H. M., van Bokhoven, H., Kolk, S. M., Homberg, J. R., & Zhou, H. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhw407 · Cited by 22
Self-citationÁdám, Á., Kemecsei, R., Murcia‐Ramón, R., Juárez-Leal, I., Gerecsei, L. I., Zachár, G., Echevarrı́a, D., Puelles, E., Martı́nez, S., & Csillag, A. (2020) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2020.00029 · Cited by 19
Role of neuropilin‐2 in the ipsilateral growth of midbrain dopaminergic axons
Torigoe, M., Yamauchi, K., Tamada, A., Matsuda, I., Aiba, A., Castellani, V., & Murakami, F. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12190 · Cited by 16
Mest/Peg1 Is Essential for the Development and Maintenance of a SNc Neuronal Subset
Mesman, S., van Hooft, J. A., & Smidt, M. P. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00166 · Cited by 16
Self-citationQureshi, M., Hatem, M., Alroughani, R., Jacob, S. P., & Al-Temaimi, R. A. (2017) · NeuroMolecular Medicine · doi:10.1007/s12017-017-8443-0 · Cited by 14
Establishing functionally segregated dopaminergic circuits
Terauchi, A., Johnson‐Venkatesh, E., & Umemori, H. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2024.12.002 · Cited by 12
Tcf4 Is Involved in Subset Specification of Mesodiencephalic Dopaminergic Neurons
Mesman, S., Wever, I., & Smidt, M. P. (2021) · Biomedicines · doi:10.3390/biomedicines9030317 · Cited by 12
Self-citationAscending midbrain dopaminergic axons require descending GAD65 axon fascicles for normal pathfinding
García‐Peña, C. M., Kim, M. K., Frade-Pérez, D., Ávila‐González, D., Téllez, E., Mastick, G. S., Tamaríz, E., & Varela‐Echavarría, A. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00043 · Cited by 12
MicroRNA-338 modulates cortical neuronal placement and polarity
Kos, A., de Mooij-Malsen, A. J., van Bokhoven, H., Kaplan, B. B., Martens, G. J. M., Kolk, S. M., & Aschrafi, A. (2017) · RNA Biology · doi:10.1080/15476286.2017.1325067 · Cited by 12
Self-citationThe generation of midbrain dopaminergic neurons
Blaess, S., Stott, S., & Ang, S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814405-3.00017-5 · Cited by 12
Schmidt, E. R. E., Morello, F., & Pasterkamp, R. J. (2012) · Journal of Visualized Experiments · doi:10.3791/3691 · Cited by 12
Self-citationAnatomical Development of the Cerebellothalamic Tract in Embryonic Mice
Dumas, D. B., Gornati, S. V., Adolfs, Y., Shimogori, T., Pasterkamp, R. J., & Hoebeek, F. E. (2022) · Cells · doi:10.3390/cells11233800 · Cited by 11
Self-citationView Point: Semaphorin-3E: An Emerging Modulator of Natural Killer Cell Functions?
Alamri, A., GOUNNI, A. S., & Kung, S. K. P. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18112337 · Cited by 11
The role of Wnt, ARL4C, and Sema3A in developmental process and disease pathogenesis
Fujii, S., & Kiyoshima, T. (2023) · Pathology International · doi:10.1111/pin.13325 · Cited by 11
Increased innervation of forebrain targets by midbrain dopaminergic neurons in the absence of FGF-2
Rumpel, R., Baron, O., Ratzka, A., Schröder, M., Hohmann, M., Effenberg, A., Claus, P., & Grothe, C. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.057 · Cited by 10
Polymethacryloyl-L-Phenylalanine [PMAPA]-Based Monolithic Column for Capillary Electrochromatography
Derazshamshir, A., Aşır, S., Göktürk, I., Ektirici, S., Yılmaz, F., & Deni̇zli̇, A. (2019) · Journal of Chromatographic Science · doi:10.1093/chromsci/bmz047 · Cited by 9
Transplantation in the nonhuman primate MPTP model of Parkinson's disease: update and perspectives
Wianny, F., & Vezoli, J. (2017) · Primate Biology · doi:10.5194/pb-4-185-2017 · Cited by 8
Dynamic Insights into Dopamine Axon Growth in Adolescence and its Implications for Psychiatric Risk
Avramescu, R. G., Capolicchio, T., & Flores, C. (2024) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2024.101435 · Cited by 8
Circular RNAs regulate neuron size and migration of midbrain dopamine neurons during development
Rybiczka-Tešulov, M., Garritsen, O., Venø, M. T., Wieg, L., van Dijk, R. E., Rahimi, K., Gomes‐Duarte, A., de Wit, M., van de Haar, L. L., Michels, L., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-51041-1 · Cited by 7
Self-citationLi, Q., Ma, N., Li, X., Yang, C., Zhang, W., Xiong, J., Zhu, L., Li, J., Wen, Q., Gao, L., et al. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002686 · Cited by 7
Jahan, M. S., Tsuzuki, T., Ito, T., Bhuiyan, M. E. R., Takahashi, I., Takamatsu, H., Kumanogoh, A., Negishi, T., & Yukawa, K. (2022) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2022.11.002 · Cited by 7
Fibroblast Growth Factor: Promising Target for Schizophrenia
Talaeı, A., Farkhondeh, T., & Forouzanfar, F. (2020) · Current Drug Targets · doi:10.2174/1389450121666200628114843 · Cited by 6
Tgfbr2 in Dental Pulp Cells Guides Neurite Outgrowth in Developing Teeth
Stanwick, M., Barkley, C., Serra, R. A., Kruggel, A., Webb, A., Zhao, Y., Pietrzak, M., Ashman, C., Staats, A., Shahid, S., et al. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.834815 · Cited by 5
Functions of Neuropilins in Wiring the Nervous System and Their Role in Neurological Disorders
Shiflett, M. W., Martinez, E. A., Khdour, H. Y., & Tran, T. S. (2017) · Springer eBooks · doi:10.1007/978-3-319-48824-0_8 · Cited by 4
Self-citationNovel vertebrate- and brain-specific driver of neuronal outgrowth
Jansen, E. J. R., van Bakel, N. H. M., Benedict, B., Loohuis, N. F. M. O., Hafmans, T. G. M., Chim, S. M., Xu, J., Kolk, S. M., & Martens, G. J. M. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.102069 · Cited by 4
Self-citationThe organizational role of ovarian hormones during puberty on risk for binge-like eating in rats
Hildebrandt, B. A., Lee, J. R., Culbert, K. M., Sisk, C. L., Johnson, A. W., & Klump, K. L. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114177 · Cited by 3
Choi, H., Oh, D., Jawad, A., Haomiao, Z., Ham, J., Heo, J., Oh, A., Jin, H., Seo, J., Oh, B. C., et al. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04693-9 · Cited by 2
Increased BMI and late-life mobility dysfunction; overlap of genetic effects in brain regions
Chang, X., Chua, K. Y., Ng, F. L., Wang, L., Liu, J., Yuan, J., Khor, C. C., Heng, C., Dorajoo, R., & Koh, W. (2023) · International Journal of Obesity · doi:10.1038/s41366-023-01275-8 · Cited by 2
Falk, J., & Castellani, V. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00002-8 · Cited by 2
Semaphorin Regulation of Neural Circuit Assembly in the Central Nervous System
Hand, R., & Kolodkin, A. L. (2015) · Springer eBooks · doi:10.1007/978-4-431-54385-5_2 · Cited by 2
Self-citationToutain, A., Scotto‐Lomassese, S., Muzerelle, A., Puech, J., Fayad, A., Roumier, A., Hervé, D., & Métin, C. (2026) · European Journal of Neuroscience · doi:10.1111/ejn.70385 · Cited by 1
Hoops, D., Yee, Y., Hammill, C. F., Wong, S., Manitt, C., Bedell, B. J., Cahill, L. S., Lerch, J. P., Flores, C., & Sled, J. G. (2024) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.230106 · Cited by 1
Grealish, S. (2012) · Lund University Publications (Lund University)
Metadata
- Authors
- Kolk, S. M., Gunput, R.-A. F., Tran, T. S., van den Heuvel, D. M. A., Prasad, A. A., Hellemons, A. J. C. G. M., Adolfs, Y., Ginty, D. D., Kolodkin, A. L., Burbach, J. P. H., Smidt, M. P., & Pasterkamp, R. J.
- Affiliations
- University Medical Center Utrecht (NL)
- Utrecht University (NL)
- Howard Hughes Medical Institute (US)
- ORCID
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2009-10-07
- Volume
- 29
- Issue
- 40
- Pages
- 12542-12557
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC3097132
- OpenAlex
- W2142820387
- Cited by
- 114
- References
- 77
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 5 · 2023: 6 · 2022: 4 · 2021: 8 · 2020: 7 · 2019: 8 · 2018: 3 · 2017: 13 · 2016: 2 · 2015: 8 · 2014: 6 · 2013: 11 · 2012: 12
- FWCI
- 3.74
- 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)
- Radboud Repository (Radboud University) (submittedVersion)
- Radboud Repository (Radboud University) (submittedVersion, other-oa)
- Funders
- Howard Hughes Medical Institute
- National Alliance for Research on Schizophrenia and Depression
- Parkinsonfonden
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Keywords
- SEMA3F, neuropilin-2, axon fasciculation, chemoattraction, chemorepulsion, axon targeting, medial prefrontal cortex, axon orientation, dopaminergic neuron development
- MeSH terms
- Animals, Axons, Diencephalon, Dopamine, Immunohistochemistry, Membrane Proteins, Mice, Inbred C57BL, Mice, Mutant Strains, Nerve Tissue Proteins, Neurons, Neurites, Prosencephalon, Body Patterning, Protein Transport, Neuropilin-2, Tissue Culture Techniques, Mice
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