Cited by 597Axon Guidance and Neuronal SignalingNeurogenesis and neuroplasticity mechanismsVisual perception and processing mechanisms

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Growth and Reshaping of Axons in the Establishment of Visual Callosal Connections

Innocenti, G. M.·1981·Science

DOI 10.1126/science.7221566

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Abstract

The visual cortical areas in the two hemispheres are interconnected by axons running through the corpus callosum. In adult cats, these axons originate from, and terminate in, tangentially restricted portions of each area. In young kittens, however, callosal axons originate from the entire extent of each area, although they apparently enter the gray matter only in the restricted regions where they will also be found in adults. In kittens, but not in adults, callosal axons also reach other regions, but there they appear to be confined to the lowest part of layer VI. During the first two postnatal months, the callosal efferent zones become progressively restricted to their adult locations. During this process, many neurons eliminate the axons (or axon collaterals) that they had formerly sent through the corpus callosum and form permanent connections ipsilaterally.

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Two new fluorescent retrograde neuronal tracers which are transported over long distances
Bentivoglio, M., Kuypers, H. G. J. M., Catsman‐Berrevoets, C. E., Loewe, H., & Dann, O. (1980) · Neuroscience Letters · doi:10.1016/0304-3940(80)90208-6 · Cited by 442
Columnar distribution of cortico-cortical fibers in the frontal association, limbic, and motor cortex of the developing rhesus monkey
Goldman, P. S., & Nauta, W. J. H. (1977) · Brain Research · doi:10.1016/0006-8993(77)90453-x · Cited by 414
Double retrograde neuronal labeling through divergent axon collaterals, using two fluorescent tracers with the same excitation wavelength which label different features of the cell
Kuypers, H. G. J. M., Bentivoglio, M., Catsman‐Berrevoets, C. E., & Bharos, A. T. (1980) · Experimental Brain Research · doi:10.1007/bf00236147 · Cited by 406
Exuberant projection into the corpus callosum from the visual cortex of newborn cats
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Fluorescent retrograde neuronal labeling in rat by means of substances binding specifically to adeninethymine rich DNA
Bentivoglio, M., Kuypers, H. G. J. M., Catsman‐Berrevoets, C. E., & Dann, O. (1979) · Neuroscience Letters · doi:10.1016/0304-3940(79)96068-3 · Cited by 206
Anatomy of interhemispheric connections in the visual system of Boston Siamese and ordinary cats
Shatz, C. J. (1977) · The Journal of Comparative Neurology · doi:10.1002/cne.901730307 · Cited by 194
Differential distribution of callosal projection neurons in the neonatal and adult rat
Ivy, G. O., Akers, R. M., & Killackey, H. P. (1979) · Brain Research · doi:10.1016/0006-8993(79)90247-6 · Cited by 166

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Yakovlev, P. I., Regional Development of the Brain in Early Life: 3 (1967).

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Self-citation
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Fryer, R. H., Kaplan, D. R., Feinstein, S. C., Radeke, M. J., Grayson, D. R., & Kromer, L. F. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19961007)374:1 · Cited by 273
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The development of auditory callosal connections in normal and hypothyroid rats
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Multiple sets of visual cortical neurons projecting transitorily through the corpus callosum
Innocenti, G. M., & Clarke, S. (1983) · Neuroscience Letters · doi:10.1016/0304-3940(83)90218-5 · Cited by 62
Self-citation
Neuroimaging of Developmental Psychopathologies: The Importance of Self‐Regulatory and Neuroplastic Processes in Adolescence
SPESSOT, A. L., PLESSEN, K. J., & PETERSON, B. S. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1308.010 · Cited by 61
Staining of regenerated optic arbors in goldfish tectum: Progressive changes in immature arbors and a comparison of mature regenerated arbors with normal arbors
Schmidt, J. T., Turcotte, J. C., Buzzard, M., & Tieman, D. G. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902690408 · Cited by 61
Emergence of callosally projecting neurons with stellate morphology in the visual cortex of the kitten
Vercelli, A., Assal, F., & Innocenti, G. M. (1992) · Experimental Brain Research · doi:10.1007/bf00227248 · Cited by 60
Self-citation
NGF-induced remodeling of mature uninjured axon collaterals
Saffran, B. N., & Crutcher, K. A. (1990) · Brain Research · doi:10.1016/0006-8993(90)91315-8 · Cited by 60
Postnatal development of afferent projections to the lateral suprasylvian visual area in the cat: An HRP study
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Tolbert, D. L., & Der, T. C. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902600210 · Cited by 60
Development of Y‐axon innervation of cortical area 18 in the cat.
Friedlander, M. J., & Martin, K. A. C. (1989) · The Journal of Physiology · doi:10.1113/jphysiol.1989.sp017756 · Cited by 59
Binocular interaction in the fetal cat regulates the size of the ganglion cell population
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O’Leary, D. D. M. (2007) · Novartis Foundation symposium · doi:10.1002/9780470513422.ch8 · Cited by 59

Authors: Innocenti, G. M.
Affiliations: University of Lausanne (CH)
Corresponding author: Innocenti, G. M.
Venue: Science
Publisher: American Association for the Advancement of Science (AAAS)
Published: 1981-05-15
Volume: 212
Issue: 4496
Pages: 824-827
ISSN: 0036-8075 (ISSN-L)
1095-9203
DOI: 10.1126/science.7221566
OpenAlex: W1978268702
Cited by: 597
References: 15
Citations by year: 2026: 3 · 2025: 4 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 4 · 2019: 4 · 2018: 3 · 2017: 4 · 2016: 5 · 2015: 5 · 2014: 3 · 2013: 8 · 2012: 6
FWCI: 14.12
Type: journal article
Language: en
Open access: closed
Locations: Science (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Keywords: corpus callosum, callosal axons, visual cortex, axon growth, axon pruning, postnatal development, kittens, cats, axon collaterals, layer 6
MeSH terms: Age Factors, Animals, Axons, Cats, Corpus Callosum, Visual Pathways

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Growth and Reshaping of Axons in the Establishment of Visual Callosal Connections

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