Cited by 1,110Neurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

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Rat hippocampal neurons in dispersed cell culture.

Banker, Gary A., Cowan, W. Maxwell·1977·Brain Research

DOI 10.1016/0006-8993(77)90594-7

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Abstract

An in vitro system has been developed for the study of isolated hippocampal neurons from 18- or 19-day rat fetuses. Following trypsinization the cells are plated out at low density on polylysine-treated coverslips in an enriched medium. The isolated neurons rapidly attach to the substrate and initiate process extension. Little reaggregation occurs and the number of non-neuronal cells present is minimal. Unless co-cultured with tissue explants the neurons survive for only a few days; in the presence of hippocampal explants the initial growth of the isolated cells is improved and their survival in culture is extended to about two weeks. Some of the cells in such cultures develop a characteristic branching pattern closely resembling that of maturing hippocampal pyramidal cells in vivo. There is a clear relationship between the stage of the cells' development and their growth in culture. Cells which had completed DNA synthesis about 48 h before dissociation, and which were in the process of migration to the cortical plate, survived best in our cultures. Early post-mitotic cells which were still within the ventricular zone and cells which had already reached the cortical plate grew poorly. This system should permit the study not only of process formation by these cells, but also of their capacity to form specific synapses in vitro and of the biochemical constituents of their surfaces.

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Studies on the structure of the cerebral cortex. II. Continuation of the study of the ammonic system.
de Nó, R. L. (1934) · Cited by 1,974
The autoradiographic demonstration of axonal connections in the central nervous system
Cowan, W. M., Gottlieb, D. I., Hendrickson, A. E., Price, J. L., & Woolsey, T. A. (1972) · Brain Research · doi:10.1016/0006-8993(72)90344-7 · Cited by 1,610
Self-citation
An autoradiographic study of the time of origin and the pattern of granule cell migration in the dentate gyrus of the rat
Schlessinger, A. R., Cowan, W. M., & Gottlieb, D. I. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901590202 · Cited by 731
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ATTACHMENT AND CULTURE OF DISSOCIATED CELLS FROM RAT EMBRYO CEREBRAL HEMISPHERES ON POLYLYSINE-COATED SURFACE
Yavin, E., & Yavin, Z. (1974) · The Journal of Cell Biology · doi:10.1083/jcb.62.2.540 · Cited by 470
Synapse formation between dissociated nerve and muscle cells in low density cell cultures
Fischbach, G. D. (1972) · Developmental Biology · doi:10.1016/0012-1606(72)90023-1 · Cited by 458
FINE STRUCTURE OF NERVE FIBERS AND GROWTH CONES OF ISOLATED SYMPATHETIC NEURONS IN CULTURE
Bunge, M. (1973) · Journal of Cell Biology · doi:10.1083/jcb.56.3.713 · Cited by 452
Possible roles for cell-to-substratum adhesion in neuronal morphogenesis
Letourneau, P. C. (1975) · Developmental Biology · doi:10.1016/0012-1606(75)90378-4 · Cited by 444
PRIMARY CULTURES OF DISSOCIATED SYMPATHETIC NEURONS
Mains, R. E., & Patterson, P. H. (1973) · The Journal of Cell Biology · doi:10.1083/jcb.59.2.329 · Cited by 425
Surface Movements during the Growth of Single Explanted Neurons
Bray, D. (1970) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.65.4.905 · Cited by 372
A SILVER METHOD FOR PARAFFIN SECTIONS OF NEURAL TISSUE>
SEVIER, A. C., & Munger, B. L. (1965) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/00005072-196501000-00012 · Cited by 354

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Cotman, 1974, The making of a synapse, Vol. 1, 1

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Ould‐Yahoui, A., Tremblay, E. C., Sbai, O., Ferhat, L., Bernard, A., Charrat, E., Gueye, Y., Lim, N. H., Brew, K., Risso, J., et al. (2009) · PLoS ONE · doi:10.1371/journal.pone.0008289 · Cited by 76
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Morris, J. F., Singh, J. M., & Eberwine, J. H. (2011) · Journal of Visualized Experiments · doi:10.3791/2634 · Cited by 68
The methylated-DNA binding protein MBD2 enhances NGFI-A (egr-1)-mediated transcriptional activation of the glucocorticoid receptor
Weaver, I. C. G., Hellstrom, I. C., Brown, S. E., Andrews, S. D., Dymov, S., Diorio, J., Zhang, T.-Y., Szyf, M., & Meaney, M. J. (2014) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2013.0513 · Cited by 67
Analysis of SNAP-25 immunoreactivity in hippocampal inhibitory neurons during development in culture and in situ
Frassoni, C., Inverardi, F., Coco, S., Ortino, B., Grumelli, C., Pozzi, D., Verderio, C., & Matteoli, M. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.11.042 · Cited by 67
Gravin Orchestrates Protein Kinase A and β2-Adrenergic Receptor Signaling Critical for Synaptic Plasticity and Memory
Havekes, R., Canton, D. A., Park, A. J., Huang, T., Nie, T., Day, J. P., Guercio, L. A., Grimes, Q., Luczak, V., Gelman, I. H., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.3612-12.2012 · Cited by 68
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Rigoni, M., Schiavo, G., Weston, A., Caccin, P., Allegrini, F., Pennuto, M., Valtorta, F., Montecucco, C., & Rossetto, O. (2004) · Journal of Cell Science · doi:10.1242/jcs.01218 · Cited by 67
Role of MAP1B in axonal retrograde transport of mitochondria
Jiménez-Mateos, E.-M., González-Billault, C., Dawson, H. N., Vitek, M. P., & Avila, J. (2006) · Biochemical Journal · doi:10.1042/bj20060205 · Cited by 70
Astrocytic nitric oxide triggers tau hyperphosphorylation in hippocampal neurons.
Saez, T. E., Pehar, M., Vargas, M. R., Barbeito, L., & Maccioni, R. B. (2004) · PubMed · Cited by 67
The Development of Neuronal Polarity: A Retrospective View
Banker, G. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1372-16.2018 · Cited by 72
Self-citation
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Schuchmann, S., Müller, W. S., & Heinemann, U. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-18-07216.1998 · Cited by 65
Eps8 controls dendritic spine density and synaptic plasticity through its actin‐capping activity
Menna, E., Zambetti, S., Morini, R., Donzelli, A., Disanza, A., Calvigioni, D., Braida, D., Nicolini, C., Orlando, M., Fossati, G., et al. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.107 · Cited by 68
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Gleixner, R. J., & Fromherz, P. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.072587 · Cited by 65
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Kim, Y., & Wu, C. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-10-03245.1987 · Cited by 65
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Eshhar, N., Petralia, R. S., Winters, C. A., Niedzielski, A. S., & Wenthold, R. J. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90040-m · Cited by 65
Glial cells contribute more to iron and aluminum accumulation but are more resistant to oxidative stress than neuronal cells
Oshiro, S., Kawahara, M., Kuroda, Y., Zhang, C., Cai, Y., Kitajima, S., & Shirao, M. (2000) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/s0925-4439(00)00065-x · Cited by 64
Early dendrite development in spinal cord cell cultures: A quantitative study
Neale, E. A., Bowers, L. M., & Smith, T. G. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490340107 · Cited by 64
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Vassanelli, S., & Fromherz, P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06767.1999 · Cited by 64
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Liu, Z., Geng, L., Li, R., He, X., Zheng, J. Q., & Xie, Z. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-10-04156.2003 · Cited by 62
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Dankovich, T. M., Kaushik, R., Olsthoorn, L. H. M., Petersen, G. C., Giro, P. E., Kluever, V., Agüi‐Gonzalez, P., Grewe, K., Bao, G., Beuermann, S., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27462-7 · Cited by 64
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Braun, D., & Fromherz, P. (2004) · Biophysical Journal · doi:10.1529/biophysj.104.039990 · Cited by 63
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Mattson, M. P., Guthrie, P., Hayes, B., & Kater, S. B. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-04-01223.1989 · Cited by 63
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Shitaka, Y., Matsuki, N., Saitō, H., & Katsuki, H. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06476.1996 · Cited by 62
Central nervous system neurons migrate on astroglial fibers from heterotypic brain regions in vitro.
GASSER, U. E., & Hatten, M. E. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.12.4543 · Cited by 62

Authors: Banker, G. A., & Cowan, W. M.
Affiliations: Washington University in St. Louis (US)
ORCID: Banker, Gary A.
Venue: Brain Research
Publisher: Elsevier BV
Published: 1977-05
Volume: 126
Issue: 3
Pages: 397-425
ISSN: 0006-8993 (ISSN-L)
DOI: 10.1016/0006-8993(77)90594-7
OpenAlex: W1987700551
Cited by: 1,110
References: 28
Citations by year: 2026: 6 · 2025: 12 · 2024: 7 · 2023: 10 · 2022: 14 · 2021: 18 · 2020: 23 · 2019: 20 · 2018: 24 · 2017: 16 · 2016: 21 · 2015: 24 · 2014: 34 · 2013: 19 · 2012: 26
FWCI: 3.72
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Brain Research (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords: hippocampal neurons, neuronal isolation, neuronal survival, cortical plate, ventricular zone, neuronal migration, DNA synthesis, synaptogenesis
MeSH terms: Animals, Axons, Cell Aggregation, Cell Division, Cell Movement, Cell Survival, Cells, Cultured, Hippocampus, Neurons, Rats

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Rat hippocampal neurons in dispersed cell culture.

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