Principal cell activity induces spine relocation of adult-born interneurons in the olfactory bulb
Open accessAbstract
Adult-born neurons adjust olfactory bulb (OB) network functioning in response to changing environmental conditions by the formation, retraction and/or stabilization of new synaptic contacts. While some changes in the odour environment are rapid, the synaptogenesis of adult-born neurons occurs over a longer time scale. It remains unknown how the bulbar network functions when rapid and persistent changes in environmental conditions occur but when new synapses have not been formed. Here we reveal a new form of structural remodelling where mature spines of adult-born but not early-born neurons relocate in an activity-dependent manner. Principal cell activity induces directional growth of spine head filopodia (SHF) followed by spine relocation. Principal cell-derived glutamate and BDNF regulate SHF motility and directional spine relocation, respectively; and spines with SHF are selectively preserved following sensory deprivation. Our three-dimensional model suggests that spine relocation allows fast reorganization of OB network with functional consequences for odour information processing.
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?
These observations confirm that spine head filopodia induction might trigger spine switching and potentially the replacement of inefficient with more efficient synapses.
“These observations confirm that spine head filopodia induction might trigger spine switching and potentially the replacement of inefficient with more efficient synapses41,42,53.”
From Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction (2018) · cites this paper as [42]
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
The NEURON Simulation Environment
Hines, M. L., & Carnevale, N. T. (1997) · Neural Computation · doi:10.1162/neco.1997.9.6.1179 · Cited by 2,630 · see citing works
Rapid Dendritic Morphogenesis in CA1 Hippocampal Dendrites Induced by Synaptic Activity
Maletić‐Savatić, M., Malinow, R., & Svoboda, K. (1999) · Science · doi:10.1126/science.283.5409.1923 · Cited by 1,189 · see citing works
LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite
Toni, N., Buchs, P.-A., Nikonenko, I., Bron, C. R., & Muller, D. (1999) · Nature · doi:10.1038/46574 · Cited by 949 · see citing works
Becoming a new neuron in the adult olfactory bulb
Carleton, A., Petreanu, L., Lansford, R. D., Álvarez-Buylla, A., & Lledo, P. (2003) · Nature Neuroscience · doi:10.1038/nn1048 · Cited by 808 · see citing works
Enwere, E. K., Shingo, T., Gregg, C., Fujikawa, H., Ohta, S., & Weiss, S. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2751-04.2004 · Cited by 549 · see citing works
Glutamate receptors regulate actin-based plasticity in dendritic spines
Fischer, M., Kaech, S., Wagner, U., Brinkhaus, H., & Matus, A. (2000) · Nature Neuroscience · doi:10.1038/78791 · Cited by 446 · see citing works
Spine neck plasticity regulates compartmentalization of synapses
Tønnesen, J., Katona, G., Rózsa, B., & Nägerl, U. V. (2014) · Nature Neuroscience · doi:10.1038/nn.3682 · Cited by 444 · see citing works
Glutamate induces de novo growth of functional spines in developing cortex
Kwon, H.-B., & Sabatini, B. L. (2011) · Nature · doi:10.1038/nature09986 · Cited by 368 · see citing works
Male pheromone–stimulated neurogenesis in the adult female brain: possible role in mating behavior.
Mak, G. K., Enwere, E. K., Gregg, C., Pakarainen, T., POUTANEN, M. H., Huhtaniemi, I. T., & Weiss, S. (2007) · Nature Neuroscience · doi:10.1038/nn1928 · Cited by 314 · see citing works
Activity-Dependent Dynamic Microtubule Invasion of Dendritic Spines
Hu, X., Viesselmann, C., Nam, S., Merriam, E. B., & Dent, E. W. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.3074-08.2008 · Cited by 291 · see citing works
In VivoWhole-Cell Recording of Odor-Evoked Synaptic Transmission in the Rat Olfactory Bulb
Cang, J., & Isaacson, J. S. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04108.2003 · Cited by 272 · see citing works
Breton‐Provencher, V., Lemasson, M., Peralta, M. R., & Saghatelyan, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3606-09.2009 · Cited by 263 · see citing works
Self-citationAdult neurogenesis promotes synaptic plasticity in the olfactory bulb
Nissant, A., Bardy, C., Katagiri, H., Murray, K., & Lledo, P. (2009) · Nature Neuroscience · doi:10.1038/nn.2298 · Cited by 252 · see citing works
Lledo, P., & Saghatelyan, A. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.005 · Cited by 248 · see citing works
Self-citationPlatel, J., Dave, K. A., Gordon, V., Lacar, B., Rubio, M. E., & Bordey, A. (2010) · Neuron · doi:10.1016/j.neuron.2010.03.009 · Cited by 225 · see citing works
Shepherd, G. M., Chen, W. R., & Greer, C. A. (2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195159561.003.0005 · Cited by 216 · see citing works
Magavi, S. S. P., Mitchell, B. D., Szentirmai, O., Carter, B. S., & Macklis, J. D. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2250-05.2005 · Cited by 215 · see citing works
Activation of adult-born neurons facilitates learning and memory
Alonso, M., Lepousez, G., Wagner, S., Bardy, C., Gabellec, M., Torquet, N., & Lledo, P. (2012) · Nature Neuroscience · doi:10.1038/nn.3108 · Cited by 215 · see citing works
Majewska, A. K., & Sur, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2636949100 · Cited by 203 · see citing works
Activity-dependent dendritic spine neck changes are correlated with synaptic strength
Araya, R., Vogels, T. P., & Yuste, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321869111 · Cited by 197 · see citing works
Fukunaga, I., Herb, J. T., Köllő, M., Boyden, E. S., & Schaefer, A. T. (2014) · Nature Neuroscience · doi:10.1038/nn.3760 · Cited by 191 · see citing works
Saghatelyan, A., Roux, P., Migliore, M., Rochefort, C., Desmaisons, D., Charneau, P., Shepherd, G. M., & Lledo, P. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.016 · Cited by 170 · see citing works
Self-citationAdult naris closure profoundly reduces tyrosine hydroxylase expression in mouse olfactory bulb
Baker, H. A., Morel, K. D., Stone, D. M., & MARUNIAK, J. A. (1993) · Brain Research · doi:10.1016/0006-8993(93)91023-l · Cited by 163 · see citing works
Whitman, M. C., & Greer, C. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1633-07.2007 · Cited by 163 · see citing works
Glutamate induces the rapid formation of spine head protrusions in hippocampal slice cultures
Richards, D. A., Mateos, J. M., Hugel, S., de Paola, V., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501881102 · Cited by 161 · see citing works
Sequential development of synapses in dendritic domains during adult neurogenesis
Kelsch, W., Lin, C.-W., & Lois, C. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807970105 · Cited by 146 · see citing works
Kelsch, W., Lin, C.-W., Mosley, C., & Lois, C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2406-09.2009 · Cited by 132 · see citing works
Dendritic development and plasticity of adult-born neurons in the mouse olfactory bulb
Mizrahi, A. (2007) · Nature Neuroscience · doi:10.1038/nn1875 · Cited by 131 · see citing works
In VivoCell Tracking With Video Rate Multimodality Laser Scanning Microscopy
Veilleux, I., Spencer, J. A., Biss, D. P., Côté, D. C., & Lin, C. P. (2008) · IEEE Journal of Selected Topics in Quantum Electronics · doi:10.1109/jstqe.2007.912751 · Cited by 129 · see citing works
Self-citationSensory Input Enhances Synaptogenesis of Adult-Born Neurons
Livneh, Y., Feinstein, N., Klein, M. E., & Mizrahi, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4105-08.2009 · Cited by 106 · see citing works
Olfactory learning promotes input-specific synaptic plasticity in adult-born neurons
Lepousez, G., Nissant, A., Bryant, A. K., Gheusi, G., Greer, C. A., & Lledo, P. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1404991111 · Cited by 92 · see citing works
Early Synapse Formation in Developing Interneurons of the Adult Olfactory Bulb
Panzanelli, P., Bardy, C., Nissant, A., Pallotto, M., Sassoé‐Pognetto, M., Lledo, P., & Fritschy, J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3034-09.2009 · Cited by 89 · see citing works
Odor Processing by Adult-Born Neurons
Livneh, Y., Adam, Y., & Mizrahi, A. (2014) · Neuron · doi:10.1016/j.neuron.2014.01.007 · Cited by 87 · see citing works
Experience-dependent plasticity of mature adult-born neurons
Livneh, Y., & Mizrahi, A. (2011) · Nature Neuroscience · doi:10.1038/nn.2980 · Cited by 80 · see citing works
Konur, S., & Yuste, R. (2004) · Journal of Neurobiology · doi:10.1002/neu.10306 · Cited by 65 · see citing works
Enhanced Synaptic Integration of Adult-Born Neurons in the Olfactory Bulb of Lactating Mothers
Kopel, H., Schechtman, E., Groysman, M., & Mizrahi, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6354-11.2012 · Cited by 64 · see citing works
Role of sensory activity on chemospecific populations of interneurons in the adult olfactory bulb
Bastien-Dionne, P.-O., David, L. S., Parent, A., & Saghatelyan, A. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22307 · Cited by 60 · see citing works
Self-citationNewborn neurons in the adult olfactory bulb: Unique properties for specific odor behavior
Breton‐Provencher, V., & Saghatelyan, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.08.001 · Cited by 60 · see citing works
Self-citationStrata, P., Tempia, F., Zagrebelsky, M., & Rossi, F. (1997) · Progress in brain research · doi:10.1016/s0079-6123(08)63369-5 · Cited by 55 · see citing works
Synaptophysin and synaptoporin expression in the developing rat olfactory system
Bergmann, M. M., Schuster, T., Grabs, D., Marquèze‐Pouey, B., Betz, H., Traurig, H. H., Mayerhofer, A., & Gratzl, M. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90009-y · Cited by 54 · see citing works
Pallotto, M., Nissant, A., Fritschy, J., Rudolph, U., Sassoé‐Pognetto, M., Panzanelli, P., & Lledo, P. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0214-12.2012 · Cited by 51 · see citing works
A model of ocular dominance column development by competition for trophic factor
Harris, A. E., Ermentrout, B., & Small, S. L. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.18.9944 · Cited by 51 · see citing works
Circuit formation and maintenance—perspectives from the mammalian olfactory bulb
Adam, Y., & Mizrahi, A. (2009) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2009.11.001 · Cited by 48 · see citing works
PIP3 Regulates Spinule Formation in Dendritic Spines during Structural Long-Term Potentiation
Ueda, Y., & Hayashi, Y. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3122-12.2013 · Cited by 45 · see citing works
Lateral Connectivity in the Olfactory Bulb is Sparse and Segregated
Kim, D. H., Phillips, M. E., Chang, A. Y., Patel, H. K., Nguyen, K. T., & Willhite, D. C. (2011) · Frontiers in Neural Circuits · doi:10.3389/fncir.2011.00005 · Cited by 44 · see citing works
Glial glutamate transport modulates dendritic spine head protrusions in the hippocampus
Verbich, D., Prenosil, G., Chang, P. K. ‐., Murai, K. K., & McKinney, R. A. (2012) · Glia · doi:10.1002/glia.22335 · Cited by 44 · see citing works
GluN2B-Containing NMDA Receptors Promote Wiring of Adult-Born Neurons into Olfactory Bulb Circuits
Kelsch, W., Li, Z., Eliava, M., Goengrich, C., & Monyer, H. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.1459-12.2012 · Cited by 40 · see citing works
English, C. N., Vigers, A. J., & Jones, K. R. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206492109 · Cited by 36 · see citing works
Bergami, M., Vignoli, B., Motori, E., Pifferi, S., Zuccaro, E., Menini, A., & Canossa, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4812-12.2013 · Cited by 34 · see citing works
Breton‐Provencher, V., Côté, D. C., & Saghatelyan, A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3013-13.2014 · Cited by 33 · see citing works
Self-citationSynaptic clusters function as odor operators in the olfactory bulb
Migliore, M., Cavarretta, F., Marasco, A., Tulumello, E., Hines, M. L., & Shepherd, G. M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1502513112 · Cited by 30 · see citing works
Self-citationMechanisms and benefits of granule cell latency coding in the mouse olfactory bulb
Giridhar, S., & Urban, N. N. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00040 · Cited by 9 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Shepherd G. M., Chen W. R. & Greer C. A. in The Synaptic Organization of the Brain ed. Shepherd G. M. 165– 216Oxford Univ. Press (2004).
Cited by
Sorted by citations
Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
Weinhard, L., di Bartolomei, G., Bolasco, G., Machado, P., Schieber, N. L., Neniskyte, U., Exiga, M., Vadisiute, A., Raggioli, A., Schertel, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-03566-5 · Cited by 790 · see citing works
Microglial Remodeling of the Extracellular Matrix Promotes Synapse Plasticity
Nguyen, P. T., Dorman, L. C., Pan, S., Vainchtein, I. D., Han, R. T., Nakao-Inoue, H., Taloma, S. E., Barron, J. J., Molofsky, A. B., Kheirbek, M. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.05.050 · Cited by 615 · see citing works
Aging and Rejuvenation of Neural Stem Cells and Their Niches
Navarro Negredo, P., Yeo, R. W., & Brunet, A. (2020) · Cell Stem Cell · doi:10.1016/j.stem.2020.07.002 · Cited by 246 · see citing works
The role of microglia and their CX3CR1 signaling in adult neurogenesis in the olfactory bulb
Reshef, R., Kudryavitskaya, E., Shani-Narkiss, H., Isaacson, B., Rimmerman, N., Mizrahi, A., & Yirmiya, R. (2017) · eLife · doi:10.7554/elife.30809 · Cited by 108 · see citing works
Rewiring of Memory Circuits: Connecting Adult Newborn Neurons With the Help of Microglia
Rodríguez-Iglesias, N., Sierra, A., & Valero, J. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00024 · Cited by 74 · see citing works
Adult-born neurons boost odor-reward association
Grelat, A., Benoit, L., Wagner, S., Moigneu, C., Lledo, P.-M., & Alonso, M. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716400115 · Cited by 72 · see citing works
Alonso, S. B., Reinert, J. K., Marichal, N., Massalini, S., Berninger, B., Kuner, T., & Calegari, F. (2019) · The EMBO Journal · doi:10.15252/embj.201798791 · Cited by 69 · see citing works
Adult neurogenesis beyond the niche: its potential for driving brain plasticity
Sailor, K. A., Schinder, A. F., & Lledo, P. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.12.001 · Cited by 67 · see citing works
Synaptic pruning of murine adult-born neurons by microglia depends on phosphatidylserine
Kurematsu, C., Sawada, M., Ohmuraya, M., Tanaka, M., Kuboyama, K., Ogino, T., Matsumoto, M., Oishi, H., Inada, H., Ishido, Y., et al. (2022) · Journal of Experimental Medicine · doi:10.1084/jem.20202304 · Cited by 60 · see citing works
Pignatelli, A., & Belluzzi, O. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00007 · Cited by 65 · see citing works
Takahashi, H., Yoshihara, S., & Tsuboi, A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00229 · Cited by 50 · see citing works
Plasticity in olfactory bulb circuits
Wu, A., Yu, B., & Komiyama, T. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.01.007 · Cited by 43 · see citing works
Neural plasticity in developing and adult olfactory pathways – focus on the human olfactory bulb
Huart, C., Rombaux, P., & Hummel, T. R. (2019) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-018-9780-x · Cited by 30 · see citing works
Maldonado‐Ruiz, R., Garza‐Ocañas, L., & Camacho‐Morales, A. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.03.009 · Cited by 30 · see citing works
Forest, J., Chalençon, L., Midroit, M., Terrier, C., Caillé, I., Sacquet, J., Benetollo, C., Martin, K., Richard, M., Didier, A., et al. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz105 · Cited by 27 · see citing works
Different forms of structural plasticity in the adult olfactory bulb
Hardy, D., & Saghatelyan, A. (2017) · Neurogenesis · doi:10.1080/23262133.2017.1301850 · Cited by 25 · see citing works
Self-citationMalvaut, S., Gribaudo, S., Hardy, D., David, L. S., Daroles, L., Labrecque, S., Lebel‐Cormier, M., Chaker, Z., Côté, D. C., Koninck, P. D., et al. (2017) · Current Biology · doi:10.1016/j.cub.2017.09.058 · Cited by 25 · see citing works
Self-citationPOU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain
McClard, C. K., Kochukov, M. Y., Herman, I., Liu, Z., Eblimit, A., Moayedi, Y., Ortiz‐Guzman, J., Colchado, D., Pekarek, B. T., Panneerselvam, S., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1641-17.2017 · Cited by 27 · see citing works
The Shape of the Olfactory Bulb Predicts Olfactory Function
Yan, X., Joshi, A., Zang, Y., Assunção, F., Fernandes, H. M., & Hummel, T. R. (2022) · Brain Sciences · doi:10.3390/brainsci12020128 · Cited by 24 · see citing works
The role of calretinin-expressing granule cells in olfactory bulb functions and odor behavior
Hardy, D., Malvaut, S., Breton‐Provencher, V., & Saghatelyan, A. (2018) · Scientific Reports · doi:10.1038/s41598-018-27692-8 · Cited by 20 · see citing works
Self-citationNaffaa, M. M. (2024) · Neural Regeneration Research · doi:10.4103/nrr.nrr-d-24-00312 · Cited by 16 · see citing works
Odor hedonics coding in the vertebrate olfactory bulb
Kermen, F., Mandairon, N., & Chalençon, L. (2021) · Cell and Tissue Research · doi:10.1007/s00441-020-03372-w · Cited by 13 · see citing works
Rapid structural remodeling of peripheral taste neurons is independent of taste cell turnover
Whiddon, Z. D., Marshall, J. B., Alston, D. C., McGee, A. W., & Krimm, R. F. (2023) · PLoS Biology · doi:10.1371/journal.pbio.3002271 · Cited by 10 · see citing works
Marco-Manclús, P., Ávila‐González, D., Paredes, R. G., & Portillo, W. (2021) · Physiology & Behavior · doi:10.1016/j.physbeh.2021.113649 · Cited by 10 · see citing works
ErbB4 deficiency exacerbates olfactory dysfunction in an early-stage Alzheimer’s disease mouse model
Deng, X., Liu, X., Wei, Y.-H., Wang, K., Zhu, J., Zhong, J.-J., Zheng, J.-Y., Guo, R., Zhu, Y., Ye, Q.-H., et al. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01332-6 · Cited by 9 · see citing works
Gribaudo, S., Saraulli, D., Nato, G., Bonzano, S., Gambarotta, G., Luzzati, F., Costanzi, M., Peretto, P., Bovetti, S., & Marchis, S. D. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22084269 · Cited by 9 · see citing works
A hominoid-specific signaling axis regulating the tempo of synaptic maturation
Dong, J., Zhu, X.-N., Zeng, P.-M., Cao, D.-D., Yang, Y., Hu, J., & Luo, Z. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114548 · Cited by 7 · see citing works
Meng, J. H., & Riecke, H. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010338 · Cited by 7 · see citing works
Ferreira, A., Constantinescu, V.-S., Malvaut, S., Saghatelyan, A., & Hardy, S. V. (2024) · Communications Biology · doi:10.1038/s42003-024-06115-7 · Cited by 6 · see citing works
Self-citationDejou, J., Mandairon, N., & Didier, A. (2024) · Frontiers in Neural Circuits · doi:10.3389/fncir.2024.1467203 · Cited by 4 · see citing works
Lightweight 1-photon Miniscope for Imaging in Freely Behaving Animals at Subcellular Resolution
Bagramyan, A. (2020) · IEEE Photonics Technology Letters · doi:10.1109/lpt.2020.3004283 · Cited by 5 · see citing works
Saha, S., Meng, J. H., Riecke, H., Agoranos, G., Sailor, K. A., & Lledo, P. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.28.428612 · Cited by 4 · see citing works
New Neurons in the Postnatal Olfactory System: Functions in the Healthy and Regenerating Brain
Gregory, J. D., Kunkhyen, T., Sweat, S. C., Huang, J. S., Brechbill, T. R., & Cheetham, C. E. J. (2025) · Brain Sciences · doi:10.3390/brainsci15060597 · Cited by 4 · see citing works
Ogawa, B., Nakanishi, Y., Wakamatsu, M., Takahashi, Y., & Shibutani, M. (2023) · Toxicology Letters · doi:10.1016/j.toxlet.2023.02.004 · Cited by 3 · see citing works
Neural circuits of the mammalian main olfactory bulb
Burton, S. D., Lepousez, G., Lledo, P., & Wachowiak, M. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814411-4.00001-9 · Cited by 3 · see citing works
Adult neurogenesis reconciles flexibility and stability of olfactory perceptual memoryPreprint
Sakelaris, B. G., & Riecke, H. (2025) · eLife · doi:10.7554/elife.104443.3 · Cited by 3 · see citing works
Synaptogenesis in the adult CNS—olfactory system
Mizrahi, A., & Vinograd, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00011-9 · Cited by 2 · see citing works
Regeneration in the Olfactory Bulb
Malvaut, S., & Saghatelyan, A. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.23883-2 · Cited by 2 · see citing works
Self-citationBDNF-dependent signaling in the olfactory bulb modulates social recognition memory in mice
de Castro, C. M., Almeida‐Santos, A. F., Mansk, L. M. Z., Jaimes, L. F., Cammarota, M., & Pereira, G. S. (2024) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2024.107891 · Cited by 2 · see citing works
Rapid structural remodeling of peripheral taste fibers is independent of taste cell turnoverPreprint
Whiddon, Z. D., Marshall, J. B., Alston, D. C., McGee, A. W., & Krimm, R. (2023) · bioRxiv · doi:10.1101/2022.11.17.513266 · Cited by 1 · see citing works
Bao, S., Romero, J. M., Belfort, B. D. W., & Arenkiel, B. R. (2024) · genesis · doi:10.1002/dvg.23595 · Cited by 1 · see citing works
Timing Matters: Lessons From Perinatal Neurogenesis in the Olfactory Bulb
Liberia, T., Han, K., Spence, N. J., Meller, S. J., Martín-López, E., & Greer, C. A. (2025) · The Journal of Comparative Neurology · doi:10.1002/cne.70045 · Cited by 1 · see citing works
Meng, J. H., & Riecke, H. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.04.411629 · Cited by 1 · see citing works
Deschênes, A., Lavoie‐Cardinal, F., Méthot, M., & Koninck, P. D. (2019) · Education and Training in Optics and Photonics · doi:10.1117/12.2523459
Mira, H., Díez del Corral, R., & Morales, A. V. (2020) · Frontiers research topics · doi:10.3389/978-2-88963-988-5
Large-Scale Models of the Olfactory Bulb
Cavarretta, F. (2018) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-4614-7320-6_100664-1
Self-citationLarge-Scale Models of the Olfactory Bulb
Cavarretta, F. (2021) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-4614-7320-6_100664-2
Self-citationLarge-Scale Models of the Olfactory Bulb
Cavarretta, F. (2022) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-0716-1006-0_100664
Self-citationFerreira, A., Constantinescu, V.-S., Malvaut, S., Saghatelyan, A., & Hardy, S. V. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.20.549882
Self-citationAdult Neurogenesis Reconciles Flexibility and Stability of Olfactory Perceptual MemoryPreprint
Sakelaris, B. G., & Riecke, H. (2025) · eLife · doi:10.7554/elife.104443.1
Adult Neurogenesis Reconciles Flexibility and Stability of Olfactory Perceptual MemoryPreprint
Sakelaris, B. G., & Riecke, H. (2025) · eLife · doi:10.7554/elife.104443.2
Snapyan, M., Constantinescu, V.-S., Saghatelyan, A., & Parent, M. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1358-24.2025
Self-citationRôle et connectivité des néo-neurones formés à l’âge adulte dans le bulbe olfactif
Grelat, A. (2018) · theses.fr (ABES) · doi:10.70675/c01c4ec0zba51z466aza2f1z09fdd6310b8f
Olfactory learning potentiates long-range cortical GABAergic inputs onto adult-born neuronsPreprint
Peroni, E., Badts, C.-H. D., Lepousez, G., Hiridjee, A., Renvoise, J., Lafosse, I., Wagner, S., Jacquemet, E., Lledo, P., Alonso, M., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.29.728424
- Authors
- Breton-Provencher, V., Bakhshetyan, K., Hardy, D., Bammann, R. R., Cavarretta, F., Snapyan, M., Côté, D., Migliore, M., & Saghatelyan, A.
- Affiliations
- Institut Universitaire en Santé Mentale de Québec (CA)
- University of Milan (IT)
- Corresponding author
- Saghatelyan, Armen
- Venue
- Nature Communications
- Published
- 2016-08-31
- Volume
- 7
- Issue
- 1
- Pages
- 12659-12659
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC5013674
- OpenAlex
- W2517669168
- Cited by
- 60
- References
- 52
- Citations by year
- 2026: 1 · 2025: 7 · 2024: 7 · 2023: 6 · 2022: 5 · 2021: 5 · 2020: 9 · 2019: 7 · 2018: 7 · 2017: 5 · 2016: 1
- FWCI
- 3.40
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Cincinnati Children's Hospital Medical Center
- Helsingin Yliopisto
- Partnership for Advanced Computing in Europe AISBL
- Canadian Institutes of Health Research
- Natural Sciences and Engineering Research Council of Canada
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Keywords
- adult neurogenesis, olfactory bulb, filopodia, brain-derived neurotrophic factor, glutamate, sensory deprivation, synaptogenesis, network reorganization
- MeSH terms
- Animals, Cell Movement, Female, Image Processing, Computer-Assisted, Interneurons, Male, Mice, Inbred C57BL, Mice, Transgenic, Models, Biological, Odorants, Olfactory Bulb, Pseudopodia, Sensory Deprivation, Smell, Synapses, Glutamic Acid, Brain-Derived Neurotrophic Factor, Models, Animal, Dendritic Spines, Mice, Neurogenesis, Time-Lapse Imaging
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