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

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Rat hippocampal neurons in dispersed cell culture.

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

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

Open this paper in CoChat — free account

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.

Integrity signals

Registry

Crossref · 10.1016/0006-8993(77)90594-7

Cites

28 of 28 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

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
Self-citation
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

Show all 28 references

Research works printed but not linked: 1

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

Sorted by citations

Items 401–500 of 1,000

Fluorescence Resonance Energy Transfer Detection of Synaptophysin I and Vesicle-associated Membrane Protein 2 Interactions during Exocytosis from Single Live Synapses
Pennuto, M., Dunlap, D. D., Contestabile, A., Benfenati, F., & Valtorta, F. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e02-01-0036 · Cited by 60
γ-Interferon promotes differentiation of cultured cortical and hippocampal neurons
Barish, M. E., Mansdorf, N. B., & Raissdana, S. S. (1991) · Developmental Biology · doi:10.1016/0012-1606(91)90433-4 · Cited by 62
Stimulation of olfactory ensheathing cell motility enhances olfactory axon growth
Windus, L. C. E., Chehrehasa, F., Lineburg, K. E., Claxton, C., Mackay‐Sim, A., Key, B., & John, J. A. S. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0630-9 · Cited by 61
Interactions between Chemokines
Cook, A., Hippensteel, R., Shimizu, S., Nicolai, J., Fatatis, A., & Meucci, O. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.035477 · Cited by 62
Methylmercury exposure downregulates the expression of Racl and leads to neuritic degeneration and ultimately apoptosis in cerebrocortical neurons
Fujimura, M., Usuki, F., Sawada, M., Rostène, W. H., Godefroy, D., & Takashima, A. (2008) · NeuroToxicology · doi:10.1016/j.neuro.2008.10.002 · Cited by 61
Inhibition of AMPA receptor trafficking at hippocampal synapses by β-amyloid oligomers: the mitochondrial contribution
Rui, Y., Gu, J., Yu, K., Hartzell, H. C., & Zheng, J. Q. (2010) · Molecular Brain · doi:10.1186/1756-6606-3-10 · Cited by 62
Electrophysiology and morphology of the developing hippocampus of fetal rabbits
Schwartzkroin, P. A., & Kunkel, D. D. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-04-00448.1982 · Cited by 61
A signal located within amino acids 1-27 of GAD65 is required for its targeting to the Golgi complex region.
Solimena, M., Dirkx, R. A., Radzynski, M., Mundigl, O., & Camilli, P. V. D. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.126.2.331 · Cited by 61
Morphology of dissociated hippocampal cultures from fetal mice
Peacock, J. H., Rush, D. F., & Mathers, L. H. (1979) · Brain Research · doi:10.1016/0006-8993(79)91027-8 · Cited by 60
Neuroprotective effects of atypical D1 receptor agonist SKF83959 are mediated via D1 receptor‐dependent inhibition of glycogen synthase kinase‐3β and a receptor‐independent anti‐oxidative action
Yu, Y., Wang, J., Sun, P., Guo, Y., Zhang, Z., Jin, G.-Z., & Zhen, X. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.05062.x · Cited by 59
Effects of restraint stress on the expression of proteins involved in synaptic vesicle exocytosis in the hippocampus
Gao, Y., Bezchlibnyk, Y. B., Sun, X., Wang, J., McEwen, B. S., & Young, L. T. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.04.066 · Cited by 60
Psychotropic and neurotropic activity
Vogel, H. G., & Vogel, W. H. (1997) · Springer eBooks · doi:10.1007/978-3-662-03333-3_5 · Cited by 61
Liposome-mediated NGF gene transfection following neuronal injury: potential therapeutic applications
Zou, L., Huang, L., Hayes, R. L., Black, C., Qiu, Y. H., Perez-Polo, J. R., Le, W., Clifton, G. L., & Yang, K. (1999) · Gene Therapy · doi:10.1038/sj.gt.3300936 · Cited by 59
Antibody-Regulated Neurotoxic Function of Cell-Surface β-Amyloid Precursor Protein
Sudo, H., Jiang, H., Yasukawa, T., Hashimoto, Y., Niikura, T., Kawasumi, M., Matsuda, S., Takeuchi, Y., Aiso, S., Matsuoka, M., et al. (2000) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2000.0910 · Cited by 59
Neurons dissociated from rat myenteric plexus retain differentiated properties when grown in cell culture
Nishi, R., & Willard, A. L. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90056-9 · Cited by 58
Reduced synaptic activity and dysregulated extracellular matrix pathways in midbrain neurons from Parkinson’s disease patients
Stern, S., Lau, S., Manole, A., Rosh, I., Percia, M. M., Ezer, R. B., Shokhirev, M. N., Qiu, F., Schafer, S. T., Mansour, A. A., et al. (2022) · npj Parkinson s Disease · doi:10.1038/s41531-022-00366-z · Cited by 60
Synapsin III: Role in neuronal plasticity and disease
Porton, B., Wetsel, W. C., & Kao, H. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.07.007 · Cited by 58
Capture of Dense Core Vesicles at Synapses by JNK-Dependent Phosphorylation of Synaptotagmin-4
Bharat, V., Siebrecht, M., Burk, K., Ahmed, S., Reißner, C., Kohansal-Nodehi, M., Steubler, V., Zweckstetter, M., Ting, J. T., & Dean, C. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.084 · Cited by 58
Neurotrophin-3- and norepinephrine-mediated adrenergic differentiation and the inhibitory action of desipramine and cocaine
Zhang, J., Dix, J., Langtimm, C. J., Trusk, T. C., Schroeder, B., Hoffmann, R. G., Strosberg, A. D., Winslow, J. W., & Sieber‐Blum, M. (1997) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(199703)32:3 · Cited by 33
Chapter 27 ACTH neuropeptide stimulation of serotonergic neuronal maturation in tissue culture: modulation by hippocampal cells
Azmitia, E. C., & de Kloet, E. R. (1987) · Progress in brain research · doi:10.1016/s0079-6123(08)60217-4 · Cited by 58
Dimeric dipeptide mimetics of the nerve growth factor Loop 4 and Loop 1 activate TRKA with different patterns of intracellular signal transduction
Гудашева, Т. А., Povarnina, P. Y., Антипова, Т. А., Firsova, Y. N., Konstantinopolsky, M. A., & Середенин, С. Б. (2015) · Journal of Biomedical Science · doi:10.1186/s12929-015-0198-z · Cited by 57
Amyloid β oligomers elicit mitochondrial transport defects and fragmentation in a time-dependent and pathway-specific manner
Rui, Y., & Zheng, J. Q. (2016) · Molecular Brain · doi:10.1186/s13041-016-0261-z · Cited by 57
Low Stress Ion Conductance Microscopy of Sub-Cellular Stiffness
Clarke, R. W., Novak, P., Zhukov, A., Tyler, E. J., Cano‐Jaimez, M., Drews, A., Richards, O., Volynski, K. E., Bishop, C. L., & Klenerman, D. (2016) · Soft Matter · doi:10.1039/c6sm01106c · Cited by 60
Role of the integrin-linked kinase (ILK) in determining neuronal polarity
Guo, W., Jiang, H., Gray, V., Dedhar, S., & Rao, Y. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.03.019 · Cited by 57
Targeting of the Synaptic Vesicle Protein Synaptobrevin in the Axon of Cultured Hippocampal Neurons: Evidence for Two Distinct Sorting Steps
West, A. E., Neve, R. L., & Buckley, K. M. (1997) · The Journal of Cell Biology · doi:10.1083/jcb.139.4.917 · Cited by 57
Effect of neonatal degranulation on the morphological development of rat CA3 pyramidal neurons: Inductive role of mossy fibers on the formation of thorny excrescences
Gaïarsa, J., Beaudoin, M. E., & Ben‐Ari, Y. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903210408 · Cited by 57
Early in vitro genesis and differentiation of axons and dendrites by hippocampal neurons analyzed quantitatively with neurofilament-H and microtubule-associated protein 2 antibodies
Pennypacker, K. R., Fischer, I., & Levitt, P. R. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90047-g · Cited by 57
Isolation of a protein from bovine brain which promotes neurite extension from chick embryo cerebral cortex neurons in defined medium
KLIGMAN, D. E. (1982) · Brain Research · doi:10.1016/0006-8993(82)90955-6 · Cited by 57
Astroglial modulation of transient potassium current development in cultured mouse hippocampal neurons
Wu, R., & Barish, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01677.1994 · Cited by 56
Procedures for Culturing and Genetically Manipulating Murine Hippocampal Postnatal Neurons
Moutin, E., Hemonnot-Girard, A.-L., Seube, V., Linck, N., Rassendren, F., Perroy, J., & Compan, V. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00019 · Cited by 60
Expression of Lysophosphatidic Acid Receptor in Rat Astrocytes: Mitogenic Effect and Expression of Neurotrophic Genes
Tabuchi, S., Kume, K., Aihara, M., & Shimizu, T. (2000) · Neurochemical Research · doi:10.1023/a:1007542532395 · Cited by 56
Distinct Subsets of Syt-IV/BDNF Vesicles Are Sorted to Axons versus Dendrites and Recruited to Synapses by Activity
Dean, C., Liu, H., Staudt, T., Stahlberg, M. A., Vingill, S., Bückers, J., Kamin, D., Engelhardt, J., Jackson, M. B., Hell, S. W., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4515-11.2012 · Cited by 58
Neurodegeneration and Neuroinflammation in cdk5/p25-Inducible Mice
Muyllaert, D., Terwel, D., Kremer, A., Sennvik, K., Borghgraef, P., Devijver, H., Dewachter, I., & LEUVEN, F. V. (2008) · American Journal Of Pathology · doi:10.2353/ajpath.2008.070693 · Cited by 55
Activation of the androgen receptor alters the intracellular calcium response to glutamate in primary hippocampal neurons and modulates sarco/endoplasmic reticulum calcium ATPase 2 transcription
Foradori, C. D., Werner, S. B., Sandau, U. S., Clapp, T. R., & Handa, R. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.06.054 · Cited by 55
Nestin in immature embryonic neurons affects axon growth cone morphology and Semaphorin3a sensitivity
Bott, C. J., Johnson, C. G., Yap, C. C., Dwyer, N. D., Litwa, K., & Winckler, B. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-06-0361 · Cited by 62
Glutamate‐mediated overexpression of CD38 in astrocytes cultured with neurones
Bruzzone, S., Verderio, C., Schenk, U., Fedele, E., Zocchi, E., Matteoli, M., & FLORA, A. D. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2003.02326.x · Cited by 57
N-methyl-d-aspartate (NMDA) receptors are inactivated by trypsin
Allen, C. N., Brady, R. J., Swann, J. W., Hori, N., & Carpenter, D. O. (1988) · Brain Research · doi:10.1016/0006-8993(88)90507-0 · Cited by 55
Norepinephrine and nitric oxide promote cell survival signaling in hippocampal neurons
Patel, N., Chen, M. J., & Russo‐Neustadt, A. A. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.01.012 · Cited by 54
In vitro models of axon regeneration
Al‐Ali, H., Beckerman, S. R., Bixby, J. L., & Lemmon, V. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.01.020 · Cited by 60
Ar ion plasma surface modification on the heterostructured TaOx/InGaZnO thin films for flexible memristor synapse
Sokolov, A. S., Jeon, Y.-R., Ku, B., & Choi, C. (2020) · Journal of Alloys and Compounds · doi:10.1016/j.jallcom.2019.153625 · Cited by 54
Spatial changes in calcium signaling during the establishment of neuronal polarity and synaptogenesis.
Verderio, C., Coco, S., Fumagalli, G. F., & Matteoli, M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.126.6.1527 · Cited by 54
Expression and distribution of phosphorylated MAP1B in growing axons of cultured hippocampal neurons
Boyne, L. J., Martin, K., Hockfield, S. J., & Fischer, I. (1995) · Journal of Neuroscience Research · doi:10.1002/jnr.490400403 · Cited by 54
Hippocampal Neurons Become More Vulnerable to Glutamate after Subcritical Hypoxia: An in vitro Study
Kohmura, E., Yamada, K., Hayakawa, T., Kinoshita, A., Matsumoto, K., & MOGAMI, H. (1990) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1990.144 · Cited by 54
A synaptomic analysis reveals dopamine hub synapses in the mouse striatum
Paget-Blanc, V., Pfeffer, M. E., Pronot, M., Lapios, P., Angelo, M., Walle, R., Cordelières, F. P., Levet, F., Claverol, S., Lacomme, S., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30776-9 · Cited by 60
Synaptic expression of the high-affinity kainate receptor subunit KA2 in hippocampal cultures
Roche, K. W., & Huganir, R. L. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00253-f · Cited by 53
Identification of a developmentally regulated pathway of membrane retrieval in neuronal growth cones
Bonanomi, D., Fornasiero, E. F., Valdez, G., Halegoua, S., Benfenati, F., Menegon, A., & Valtorta, F. (2008) · Journal of Cell Science · doi:10.1242/jcs.033803 · Cited by 55
The cell adhesion molecule neuroplastin‐65 inhibits hippocampal long‐term potentiation via a mitogen‐activated protein kinase p38‐dependent reduction in surface expression of GluR1‐containing glutamate receptors
Empson, R. M., Buckby, L. E., Kraus, M., Bates, K. J., Crompton, M. R., Gundelfinger, E. D., & Beesley, P. W. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.04123.x · Cited by 53
Endothelin B receptor deficiency is associated with an increased rate of neuronal apoptosis in the dentate gyrus
Ehrenreich, H., Nau, R., Dembowski, C., Hasselblatt, M., Barth, M., Hahn, A., Schilling, L., Sirén, A., & Brück, W. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00507-2 · Cited by 53
Merlin Links to the cAMP Neuronal Signaling Pathway by Anchoring the RIβ Subunit of Protein Kinase A
Grönholm, M., Vossebein, L., Carlson, C. R., Kuja‐Panula, J., Teesalu, T., Alfthan, K., Vaheri, A. I., Rauvala, H., Herberg, F. W., Taskén, K., et al. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m306149200 · Cited by 55
ToolBox: Live Imaging of intracellular organelle transport in induced pluripotent stem cell‐derived neurons
Boecker, C. A., Olenick, M. A., Gallagher, E. R., Ward, M. E., & Holzbaur, E. L. F. (2019) · Traffic · doi:10.1111/tra.12701 · Cited by 51
Molecular Tuning of Styryl Dyes Leads to Versatile and Efficient Plasma Membrane Probes for Cell and Tissue Imaging
Collot, M., Boutant, E., Fam, K. T., Danglot, L., & Klymchenko, A. S. (2020) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.0c00023 · Cited by 52
Distribution and trafficking of JHM coronavirus structural proteins and virions in primary neurons and the OBL-21 neuronal cell line
Pasick, J. M. M., Kalicharran, K., & Dales, S. (1994) · Journal of Virology · doi:10.1128/jvi.68.5.2915-2928.1994 · Cited by 52
Decreased G-Protein-Mediated Regulation and Shift in Calcium Channel Types with Age in Hippocampal Cultures
Blalock, E. M., Porter, N. M., & Landfield, P. W. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-19-08674.1999 · Cited by 52
Block of synapse formation between cerebral cortical neurons by a protein kinase inhibitor
Kuroda, Y., Ichikawa, M., Muramoto, K., Kobayashi, K., Matsuda, Y., Ogura, A., & Kudo, Y. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90449-h · Cited by 52
Cross-species neural transplants of embryonic septal nuclei to the hippocampal formation of adult rats
Daniloff, J. K., Low, W. C., Bodony, R., & Wells, J. (1985) · Experimental Brain Research · doi:10.1007/bf00237668 · Cited by 52
VGLUT1 and VGAT are sorted to the same population of synaptic vesicles in subsets of cortical axon terminals
Fattorini, G., Verderio, C., Melone, M., Giovedı̀, S., Benfenati, F., Matteoli, M., & Conti, F. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06251.x · Cited by 51
Neurite outgrowth is driven by actin polymerization even in the presence of actin polymerization inhibitors
Chia, J. X., Efimova, N., & Svitkina, T. (2016) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-04-0253 · Cited by 47
Dextromethorphan and phencyclidine receptor ligands: Differential effects on K+- and NMDA-evoked increases in cytosolic free Ca2+ concentration
Church, J., Shacklock, J. A., & Baimbridge, K. G. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90101-x · Cited by 51
Hippocampal growth cone responses to focally applied electric fields
Davenport, R. W., & McCaig, C. (1993) · Journal of Neurobiology · doi:10.1002/neu.480240108 · Cited by 51
2-(carboxycyclopropyl)glycines: binding, neurotoxicity and induction of intracellular free Ca2+ increase
Kawai, M., Horikawa, Y., Ishihara, T., Shimamoto, K., & Ohfune, Y. (1992) · European Journal of Pharmacology · doi:10.1016/0014-2999(92)90529-d · Cited by 51
Early Improved and Late Defective Cognition Is Reflected by Dendritic Spines in Tau.P301L Mice
Kremer, A., Maurin, H., Demedts, D., Devijver, H., Borghgraef, P., & LEUVEN, F. V. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4859-11.2011 · Cited by 50
Hypoxia-induced mitochondrial and nuclear DNA damage in the rat brain
Englander, E. W., Greeley, G. H., Wang, G., Perez-Polo, J. R., & Lee, H.-M. (1999) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19991015)58:2 · Cited by 51
ELKS1 localizes the synaptic vesicle priming protein bMunc13-2 to a specific subset of active zones
Kawabe, H., Mitkovski, M., Kaeser, P. S., Hirrlinger, J., Opazo, F., Nestvogel, D., Kalla, S., Fejtova, A., Verrier, S. E., Bungers, S. R., et al. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201606086 · Cited by 50
Arginine Methylation by PRMT2 Controls the Functions of the Actin Nucleator Cobl
Hou, W., Nemitz, S., Schopper, S., Nielsen, M. L., Kessels, M. M., & Qualmann, B. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.03.007 · Cited by 50
Novel Positive Allosteric Modulators of Glutamate Transport Have Neuroprotective Properties in an in Vitro Excitotoxic Model
Falcucci, R. M., Wertz, R., Green, J. L., Meucci, O., Salvino, J. M., & Fontana, A. C. K. (2019) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.9b00061 · Cited by 52
A comparative analysis of the mobility of 45 proteins in the synaptic bouton
Reshetniak, S., Ußling, J., Perego, E., Rammner, B., Schikorski, T., Fornasiero, E. F., Truckenbrodt, S., Köster, S., & Rizzoli, S. O. (2020) · The EMBO Journal · doi:10.15252/embj.2020104596 · Cited by 47
Regulation of dendritic growth by calcium and neurotrophin signaling
Dijkhuizen, P. A., & Ghosh, A. (2004) · Progress in brain research · doi:10.1016/s0079-6123(04)47002-2 · Cited by 50
BDNF Acutely Modulates Synaptic Transmission and Calcium Signalling in Developing Cortical Neurons
He, J., Gong, H., & Luo, Q. (2005) · Cellular Physiology and Biochemistry · doi:10.1159/000087733 · Cited by 50
An oxidative stress‐mediated positive‐feedback iron uptake loop in neuronal cells
Núñez‐Millacura, C., Tapia, V., Muñoz, P., Maccioni, R. B., & Núñez, M. T. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.00971.x · Cited by 50
Notch signaling in response to excitotoxicity induces neurodegeneration via erroneous cell cycle reentry
Marathe, S. V., Liu, S., Brai, E., Kaczarowski, M., & Alberi, L. A. (2015) · Cell Death and Differentiation · doi:10.1038/cdd.2015.23 · Cited by 49
C9-ALS/FTD-linked proline–arginine dipeptide repeat protein associates with paraspeckle components and increases paraspeckle formation
Suzuki, H., Shibagaki, Y., Hattori, S., & Matsuoka, M. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1983-5 · Cited by 49
Nocodazole-dependent transport, and brefeldin A--sensitive processing and sorting, of newly synthesized membrane proteins in cultured neurons
Cid-Arregui, Á., Parton, R. G., Simons, K., & Dotti, C. G. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-06-04259.1995 · Cited by 49
Blockade of N-methyl-d-aspartate receptors prevents cyanide-induced neuronal injury in primary hippocampal cultures
Patel, M. N., Yim, G. K. W., & Isom, G. E. (1992) · Toxicology and Applied Pharmacology · doi:10.1016/0041-008x(92)90375-3 · Cited by 49
Cytoskeletal events underlying dendrite formation by cultured pigment cells
Lacour, J. ‐., Gordon, P., Eller, M. S., Bhawan, J., & Gilchrest, B. A. (1992) · Journal of Cellular Physiology · doi:10.1002/jcp.1041510210 · Cited by 50
Fetal brain implants improve maze performance in hippocampal-lesioned rats
Kimble, D. P., Bremiller, R., & Stickrod, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)91023-1 · Cited by 49
Phosphorylation of Amyloid Precursor Protein at Threonine 668 Is Essential for Its Copper-responsive Trafficking in SH-SY5Y Neuroblastoma Cells
Acevedo, K. M., Opazo, C., Norrish, D., Challis, L. M., Li, Q., White, A. R., Bush, A. I., & Camakaris, J. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.538710 · Cited by 48
Regulation of neuronal P53 activity by CXCR4
Khan, M. Z., Shimizu, S., Patel, J. P., Nelson, A., Le, M.-T., Mullen-Przeworski, A., Brandimarti, R., Fatatis, A., & Meucci, O. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.05.007 · Cited by 48
Potent blockade of sodium channels and protection of brain tissue from ischemia by BIII 890 CL
Carter, A. J., Grauert, M., Pschorn, U., Bechtel, W. D., Bartmann-Lindholm, C., Qu, Y., Scheuer, T., Catterall, W. A., & Weiser, T. W. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.040577097 · Cited by 49
Cultured hippocampal neurons from trisomy 16 mouse, a model for Down's syndrome, have an abnormal action potential due to a reduced inward sodium current
Galdzicki, Z., Coan, E. J., & Рапопорт, С. И. (1993) · Brain Research · doi:10.1016/0006-8993(93)90353-o · Cited by 47
Invited review: Guidance cue patterns and cell migration in muiticeliuiar organisms
Katz, M. J., & Lasek, R. J. (1980) · Cell Motility · doi:10.1002/cm.970010111 · Cited by 48
Glutamate-stimulated protein phosphorylation in cultured hippocampal pyramidal neurons
Scholz, W., & Palfrey, H. C. (1991) · Journal of Neuroscience · doi:10.1523/jneurosci.11-08-02422.1991 · Cited by 48
Sorting nexin 17 regulates ApoER2 recycling and reelin signaling
Sotelo, P., Farfán, P., Benitez, M. L., Bu, G., & Marzolo, M.-P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093672 · Cited by 47
Receptor-Mediated Field Effect Transistor Biosensor for Real-Time Monitoring of Glutamate Release from Primary Hippocampal Neurons
Li, Y., Jin, X., Tang, L., Lv, W.-L., Xiao, M., Zhang, Z., Gao, C., & Zhang, G. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b00832 · Cited by 47
Astrocytes are required for the oscillatory activity in cultured hippocampal neurons
Verderio, C., Bacci, A., Coco, S., Pravettoni, E., Fumagalli, G. F., & Matteoli, M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00697.x · Cited by 47
Production of nerve growth factor by β‐amyloid‐stimulated astrocytes induces p75NTR‐dependent tau hyperphosphorylation in cultured hippocampal neurons
Sáez, E. T., Pehar, M., Vargas, M. R., Barbeito, L., & Maccioni, R. B. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.20996 · Cited by 48
Neuronal Depolarization Enhances the Transcription of the Neuronal Serine Protease Inhibitor Neuroserpin
Berger, P., Kozlov, S. V., Cinelli, P., Krueger, S., Vogt, L., & Sonderegger, P. (1999) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.1999.0804 · Cited by 47
Intrinsic and extrinsic factors influencing properties and growth patterns of identified leech neurons in culture
Acklin, S., & Nicholls, J. G. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01082.1990 · Cited by 47
Individual neural cell types express immunologically distinct N-CAM forms.
Williams, R. K., Goridis, C., & Akeson, R. A. (1985) · The Journal of Cell Biology · doi:10.1083/jcb.101.1.36 · Cited by 47
Uman-type neurofilament light antibodies are effective reagents for the imaging of neurodegeneration
Shaw, G., Madorsky, I., Li, Y., Wang, Y.-S., Jorgensen, M., Rana, S. D., & Fuller, D. D. (2023) · Brain Communications · doi:10.1093/braincomms/fcad067 · Cited by 49
Genetically Engineered Analogs of Ascomycin for Nerve Regeneration
Revill, W. P., Voda, J., Reeves, C. R., Chung, L., Schirmer, A., Ashley, G. W., Carney, J. R., Fardis, M., Carreras, C. W., Zhou, Y., et al. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.034264 · Cited by 46
Evidence of apoptosis in primary neuronal cultures after heat shock
Vogel, P., Dux, E., & Wießner, C. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00458-7 · Cited by 44
Characterization of the NF2 protein merlin and the ERM protein ezrin in human, rat, and mouse central nervous system
Grönholm, M., Teesalu, T., Tyynelä, J., Piltti, K. M., Böhling, T., Wartiovaara, K., Vaheri, A. I., & Carpén, O. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.11.014 · Cited by 50
Spontaneous activity and recurrent inhibition in cultured hippocampal networks
Siebler, M., Köller, H., Stichel, C. C., Müller, H. W., & Freund, H. (1993) · Synapse · doi:10.1002/syn.890140304 · Cited by 46
Long-Term Culture of Rat Hippocampal Neurons at Low Density in Serum-Free Medium: Combination of the Sandwich Culture Technique with the Three-Dimensional Nanofibrous Hydrogel PuraMatrix
Kaneko, A., & Sankai, Y. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102703 · Cited by 43
HPC ‐1/syntaxin 1A and syntaxin 1B play distinct roles in neuronal survival
Kofuji, T., Fujiwara, T., Sanada, M., Mishima, T., & Akagawa, K. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12722 · Cited by 45
Evaluation of in vitro neuronal platforms as surrogates for in vivo whole brain systems
Belle, A. M., Enright, H. A., Sales, A. P., Kulp, K. S., Osburn, J. J., Kuhn, E. A., Fischer, N. O., & Wheeler, E. K. (2018) · Scientific Reports · doi:10.1038/s41598-018-28950-5 · Cited by 45
Distal axotomy enhances retrograde presynaptic excitability onto injured pyramidal neurons via trans-synaptic signaling
Nagendran, T., Larsen, R. S., Bigler, R. L., Frost, S. B., Philpot, B. D., Nudo, R. J., & Taylor, A. M. (2017) · Nature Communications · doi:10.1038/s41467-017-00652-y · Cited by 43
In Vitro Studies of Glucocorticoid Effects on Neurons and Astrocytesa
Bohn, M. C., O’Banion, M. K., Young, D. A., Giuliano, R. E., Hussain, S. I., Dean, D., & Cunningham, L. A. (1994) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1994.tb39241.x · Cited by 45
Influence of meningeal cells on the proliferation and maturation of rat neuroblasts in culture
Gensburger, C., Labourdette, G., & Sensenbrenner, M. (1986) · Experimental Brain Research · doi:10.1007/bf00236849 · Cited by 45
Spatial and Temporal Regulation of Ca2+/Calmodulin-Dependent Protein Kinase II Activity in Developing Neurons
Menegon, A., Verderio, C., Leoni, C., Benfenati, F., Czernik, A. J., Greengard, P., Matteoli, M., & Valtorta, F. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07016.2002 · Cited by 44

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

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

Rat hippocampal neurons in dispersed cell culture.

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks