Cited by 674Neuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanismsNeuroinflammation and Neurodegeneration Mechanisms

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Trophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture

Banker, Gary A.·1980·Science

DOI 10.1126/science.7403847

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Abstract

Astroglial cells in primary culture release factors into the medium that promote the growth and prolong the survival of rat hippocampal neurons in vitro.

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Crossref · 10.1126/science.7403847

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Growth of a rat neuroblastoma cell line in serum-free supplemented medium.
Bottenstein, J. E., & SATO, G. H. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.1.514 · Cited by 2,268
Rat hippocampal neurons in dispersed cell culture.
Banker, G. A., & Cowan, W. M. (1977) · Brain Research · doi:10.1016/0006-8993(77)90594-7 · Cited by 1,110
Self-citation
Growth and cultivation of dissociated neurons and glial cells from embryonic chick, rat and human brain in flask cultures.
Booher, J., & Sensenbrenner, M. (1972) · PubMed · Cited by 760
Adult rat brain astrocytes support survival of both NGF-dependent and NGF-insensitive neurones
Lindsay, R. M. (1979) · Nature · doi:10.1038/282080a0 · Cited by 373
Trophic Mechanisms in the Peripheral Nervous System
Varon, S. S., & Bunge, R. P. (1978) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.01.030178.001551 · Cited by 326
Further observations on hippocampal neurons in dispersed cell culture
Banker, G. A., & Cowan, W. M. (1979) · Journal of Comparative Neurology · doi:10.1002/cne.901870302 · Cited by 285
Self-citation
Nerve Growth Factor
Bradshaw, R. A. (1978) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.47.070178.001203 · Cited by 246
Neuron-glia interactions.
Varon, S. S., & Gg, S. (1979) · PubMed · Cited by 244
Induction of neurite outgrowth by a conditioned-medium factor bound to the culture substratum
Collins, F. (1978) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.75.10.5210 · Cited by 241
Survival and development in culture of dissociated parasympathetic neurons from ciliary ganglia
Helfand, S. L., Smith, G. A., & Wessells, N. K. (1976) · Developmental Biology · doi:10.1016/0012-1606(76)90174-3 · Cited by 177

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ADLER, R, NEUROSCIENCE ABSTRACTS 5: 753 (1979).
ARENANDER, A.T., NEUROSCIENCE ABSTRACTS 5: 753 (1979).
BOOHER, J, NEUROBIOLOGY 2: 97 (1972).
SCHOUSBOE, A, CELL TISSUE ORGAN CU: 441 (1977).
STEIG, P.E., NEUROSCIENCE ABSTRACTS 5: 759 (1979).
VARON, S, NEUROSCIENCES RESEARCH PROGRAM BULLETIN 17: 1 (1979).

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Blount, J. B., Kondoh, T., Pundt, L. L., Conrad, J. A., Jansen, E. M., & Low, W. C. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037286 · Cited by 1
Amyloid β-protein impairs astrocyte-mediated differentiation of hippocampal neurons
Liu, Q., Schaffner, A. E., Chang, Y. H., Maric, D., & Barker, J. L. (1998) · Neuroreport · doi:10.1097/00001756-199809140-00026 · Cited by 1
The NGF superfamily of neurotrophins: Potential treatment for Alzheimer's and Parkinson's disease
Mufson, E. J., & Sobreviela, T. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037432 · Cited by 1
Thinking about repairing thinking
Ridley, R. M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037468 · Cited by 1
Studying restoration of brain function with fetal tissue grafts: Optimal models
Silver, R., & LeSauter, J. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0003750x · Cited by 1
Multiple potential mechanisms of graft action is not a new idea
Dunnett, S. B. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037353 · Cited by 1
Lessons on transplant survival from a successful model system
Moffett, S. B. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037420 · Cited by 1
Isolation and characterisation of proliferating cells from the telencephalic vesicles of gestational-day 13 rats
Koppel, H., McDermott, K. W. G., & Lantos, P. L. (1991) · Journal of Neuroscience Methods · doi:10.1016/0165-0270(91)90165-v · Cited by 1
Neural transplants are grey matters
Anderson, B., Chatterjee, A. K., & Graham, G. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037262 · Cited by 1
The structure, operation, and functionality of intracerebral grafts
Cassel, J., & Will, B. E. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00037304 · Cited by 1
Developmental Neurobiology and the Physiopathology of Brain Injury
Moonen, G., Delrée, P., Leprince, P., Rigo, J., Rogister, B., & Lefebvre, P. P. (1988) · Springer eBooks · doi:10.1007/978-1-4613-0927-7_13 · Cited by 1
Functions of NGF on Central Cholinergic Neurons
Gage, F. H., Chen, K. S., Tuszynski, M. H., & Fagan, A. M. (1990) · doi:10.1007/978-1-349-11358-3_9 · Cited by 1
Olfactory Stem Cells From Adult Rats
Wetzig, A. R. (2007) · Griffith Research Online · doi:10.25904/1912/907 · Cited by 1
Gradual inhibition of inducible nitric oxide synthase but not of interleukin-1β production in rat microglial cells of endotoxin- treated mixed glial cell cultures
(1996) · Pure Amsterdam UMC · doi:10.1002/(sici)1098-1136(199606)17:2
Factors Promoting the Growth and Regeneration of Neuronal Cells
Skaper, S. D., Leon, A., & Toffano, G. (1989) · Neuroendocrine perspectives · doi:10.1007/978-1-4612-3554-5_3

Authors: Banker, G. A.
Affiliations: Albany Medical College (US)
Corresponding author: Banker, Gary A.
ORCID: Banker, Gary A.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 1980-08-15
Volume: 209
Issue: 4458
Pages: 809-810
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.7403847
OpenAlex: W2034038906
Cited by: 674
References: 25
Citations by year: 2026: 3 · 2025: 6 · 2024: 15 · 2023: 7 · 2022: 18 · 2021: 10 · 2020: 16 · 2019: 17 · 2018: 13 · 2017: 10 · 2016: 11 · 2015: 9 · 2014: 9 · 2013: 9 · 2012: 8
FWCI: 3.80
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
Keywords: astroglial cells, hippocampal neurons, trophic interactions, neuron-glia interactions, neuronal survival, neuronal growth, glial cell culture, rat hippocampus
MeSH terms: Animals, Astrocytes, Cell Communication, Cells, Cultured, Culture Media, Hippocampus, Nerve Growth Factors, Rats

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Trophic Interactions Between Astroglial Cells and Hippocampal Neurons in Culture

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