Cited by 3,592Neurogenesis and neuroplasticity mechanismsMemory and Neural MechanismsNeuroscience and Neuropharmacology Research

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Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats

Altman, Joseph, Das, Gopal D.·1965·Journal of Comparative Neurology

DOI 10.1002/cne.901240303

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Abstract

In the autoradiograms of young rats injected with thymidine‐H 3 many of the granule cells of the dentate gyrus were found labeled. The number of labeled cells declined rapidly with increased age at the time of injection. Histological studies showed the presence in young rats of a large germinal matrix of mitotic cells in the ependymal and subependymal layers of the third and lateral ventricles. The areal extent and cell population of this germinal pool declined rapidly from birth on, with a transient rise with a peak at about 15 days. During this latter period the number of “undifferentiated” cells near the granular layer of the dentate gyrus showed a rapid rise with a subsequent decline. The decline in the number of “undifferentiated” cells was accompanied by a rise in the number of differentiated granule cells. Cell counts in homologous parts of the dentate gyrus indicated a six‐fold increase in the number of differentiated granule cells from birth to three months. We postulated that undifferentiated cells migrate postnatally from the forebrain ventricles to the hippocampus where they become differentiated. The possible functional significance of delayed hippocampal neurogenesis is discussed with reference to our finding of incorporation of testosterone‐H 3 by cells of the hippocampus, implicating that they may function as receptors of gonadal hormones.

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Are New Neurons Formed in the Brains of Adult Mammals?
Altman, J. (1962) · Science · doi:10.1126/science.135.3509.1127 · Cited by 975
Self-citation
The Kinetics of Cellular Proliferation
(1960) · The Medical Journal of Australia · doi:10.5694/j.1326-5377.1960.tb68825.x · Cited by 938
IMPROVEMENTS IN THE COATING TECHNIQUE OF RADIOAUTOGRAPHY
Kopriwa, B. M., & Leblond, C. P. (1962) · Journal of Histochemistry & Cytochemistry · doi:10.1177/10.3.269 · Cited by 934
THE ORGANIZATION AND DUPLICATION OF CHROMOSOMES AS REVEALED BY AUTORADIOGRAPHIC STUDIES USING TRITIUM-LABELED THYMIDINEE
Taylor, J. H., Woods, P. S., & Hughes, W. L. (1957) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.43.1.122 · Cited by 832
Autoradiographic investigation of cell proliferation in the brains of rats and cats
Altman, J. (1963) · The Anatomical Record · doi:10.1002/ar.1091450409 · Cited by 623
Self-citation
The subependymal layer of the mouse brain and its cell production as shown by radioautography after thymidine‐H3 injection
Smart, I. H. M. (1961) · The Journal of Comparative Neurology · doi:10.1002/cne.901160306 · Cited by 449
MEDULLOBLASTOMA CEREBELLI
Bailey, P. (1925) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1925.02200140055002 · Cited by 399
CELLULAR PROLIFERATION IN THE MOUSE AS REVEALED BY AUTORADIOGRAPHY WITH TRITIATED THYMIDINE
Hughes, W. L., Bond, V. P., Brecher, G., Cronkite, E. P., Painter, R. B., Quastler, H., & Sherman, F. G. (1958) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.44.5.476 · Cited by 357
CEREBRAL REPRESENTATION OF PENILE ERECTION
MacLean, P. D., & Ploog, D. W. (1962) · Journal of Neurophysiology · doi:10.1152/jn.1962.25.1.29 · Cited by 258
Thymidine-H3 as a tool for the investigation of the renewal of cell populations.
Cp, L., Messier, B., & Kopriwa, B. M. (1959) · PubMed · Cited by 213

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Allen E., 1912, The cessation of mitosis in the central nervous system of the albino rat, J. Comp. Neur., 22, 547
Kjellgren K., 1944, Studien über die Entwicklung der Neuronen nach der Geburt, ihre Regeneration und die Asymmetrien ihrer Verteilung beim Menschen, Acta Psychiat. Neurol. Scand., Suppl., 29, 1

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Authors: Altman, J., & Das, G. D.
Affiliations: Massachusetts Institute of Technology (US)
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1965-06
Volume: 124
Issue: 3
Pages: 319-335
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.901240303
OpenAlex: W1980499453
Cited by: 3,592
References: 18
Citations by year: 2026: 55 · 2025: 79 · 2024: 66 · 2023: 92 · 2022: 112 · 2021: 131 · 2020: 130 · 2019: 136 · 2018: 116 · 2017: 128 · 2016: 132 · 2015: 143 · 2014: 142 · 2013: 145 · 2012: 160
FWCI: 6.21
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 14374 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: dentate gyrus granule cells, germinal matrix, ependymal layer, undifferentiated cells, cell migration, rat brain development
MeSH terms: Animals, Animals, Newborn, Autoradiography, Cell Differentiation, Hippocampus, Testosterone, Thymidine, Tritium, Rats, In Vitro Techniques

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Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats

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