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Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain
Abstract
The cytological organization and the timetable of emergence and dissolution of the transient subplate zone subjacent to the developing visual and somatosensory cortex were studied in a series of human and monkey fetal brains. Cerebral walls processed with Nissl, Golgi, electron‐microscopic, and histochemical methods show that this zone consists of migratory and postmigratory neurons, growth cones, loosely arranged axons, dendrites, synapses, and glial cells. In both species the subplate zone becomes visible at the beginning of the mid‐third of gestation as a cell‐poor/fiber‐rich layer situated between the intermediate zone and the developing cortical plate. The subplate zone appears earlier in the somatosensory than in the visual area and reaches maximal width at the beginning of the last third of gestation in both regions. At the peak of its size the ratio between the width of the subplate zone and cortical plate in the somatosensory cortex is 2:1 in monkey and 4:1 in man while in the occipital lobe these structures have about equal width in both species. The dissolution of the subplate zone begins during the last third of gestation with degeneration of some subplate neurons and the relocation of fiber terminals into the cortex. The subplate zone disappears faster in the visual than in the somatosensory area. The present results together with our previous findings support the hypothesis that the subplate zone may serve as a “waiting” compartment for transient cellular interactions and a substrate for competition, segregation, and growth of afferents originated sequentially from the brain stem, basal forebrain, thalamus, and from the ipsi‐ and contralateral cerebral hemisphere. After a variable and partially overlapping time period, these fibers enter the cortical plate while the subplate zone disappears leaving only a vestige of cells scattered throughout the subcortical white matter. A comparison between species indicates that the size and duration of the subplate zone increases during mammalian evolution and culminates in human fetuses concomitantly with an enlargement of cortico‐cortical fiber systems. The regional difference in the size, pattern, and resolution of the subplate zone correlates also with the pattern of cerebral convolutions. Our findings indicate that, contrary to prevailing notions, the subplate may not be a vestige of the phylogenetically old network but a transient embryonic structure that expanded during evolution to subserve the increasing number of its connections.
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Citations
Cites
Specification of Cerebral Cortical Areas
Rakic, P. (1988) · Science · doi:10.1126/science.3291116 · Cited by 3,127
Self-citationMode of cell migration to the superficial layers of fetal monkey neocortex
Rakic, P. (1972) · Journal of Comparative Neurology · doi:10.1002/cne.901450105 · Cited by 2,170
Self-citationRakic, P. (1974) · Science · doi:10.1126/science.183.4123.425 · Cited by 1,161
Self-citationConcurrent overproduction of synapses in diverse regions of the primate cerebral cortex
Rakic, P., Bourgeois, J.-P., Eckenhoff, M. F., Zecevic, N., & Goldman-Rakic, P. S. (1986) · Science · doi:10.1126/science.3952506 · Cited by 1,133
Self-citationSynaptogenesis in human visual cortex—evidence for synapse elimination during normal development
Huttenlocher, P. R., de Courten, C., Garey, L. J., & Van der Loos, H. (1982) · Neuroscience Letters · doi:10.1016/0304-3940(82)90379-2 · Cited by 745
Kostovic, I., & Goldman‐Rakic, P. S. (1983) · Journal of Comparative Neurology · doi:10.1002/cne.902190405 · Cited by 260
Changes in synaptic density in motor cortex of rhesus monkey during fetal and postnatal life
Zecevic, N., Bourgeois, J.-P., & Rakic, P. (1989) · Developmental Brain Research · doi:10.1016/0165-3806(89)90124-7 · Cited by 253
Self-citation
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Neurodevelopmental Trajectories of the Human Cerebral Cortex
Shaw, P., Kabani, N. J., Lerch, J. P., Eckstrand, K., Lenroot, R., Gogtay, N., Greenstein, D., Clasen, L., Evans, A., Rapoport, J. L., et al. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5309-07.2008 · Cited by 1,644
Evolution of the neocortex: a perspective from developmental biology
Rakic, P. (2009) · Nature reviews. Neuroscience · doi:10.1038/nrn2719 · Cited by 1,565
Self-citationIntellectual ability and cortical development in children and adolescents
Shaw, P., Greenstein, D., Lerch, J., Clasen, L., Lenroot, R., Gogtay, N., Evans, A., Rapoport, J., & Giedd, J. (2006) · Nature · doi:10.1038/nature04513 · Cited by 1,543
Normal development of brain circuits
Tau, G. Z., & Peterson, B. S. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2009.115 · Cited by 1,391
Kadoshima, T., Sakaguchi, H., Nakano, T., Soen, M., Ando, S., Eiraku, M., & Sasai, Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1315710110 · Cited by 999
Akbarian, S. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160008002 · Cited by 1,002
Development of the human cerebral cortex: Boulder Committee revisited
Bystron, I., Blakemore, C., & Rakic, P. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2252 · Cited by 977
Self-citationOgawa, M., Miyata, T., Nakajimat, K., Yagyu, K., Seike, M., Ikenaka, K., Yamamoto, H., & Mikoshibat, K. (1995) · Neuron · doi:10.1016/0896-6273(95)90329-1 · Cited by 889
The Cellular and Molecular Landscapes of the Developing Human Central Nervous System
Silbereis, J. C., Pochareddy, S., Zhu, Y., Li, M., & Sestan, N. (2016) · Neuron · doi:10.1016/j.neuron.2015.12.008 · Cited by 818
Consciousness without a cerebral cortex: A challenge for neuroscience and medicine
Merker, B. (2007) · Behavioral and Brain Sciences · doi:10.1017/s0140525x07000891 · Cited by 868
Longitudinal Analysis of Neural Network Development in Preterm Infants
Smyser, C. D., Inder, T. E., Shimony, J. S., Hill, J. E., Degnan, A. J., Snyder, A. Z., & Neil, J. J. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq035 · Cited by 791
Smart, I. H. M. (2002) · Cerebral Cortex · doi:10.1093/cercor/12.1.37 · Cited by 687
Allendoerfer, K. L., & Shatz, C. J. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001153 · Cited by 653
Cell-cycle control and cortical development
Dehay, C., & Kennedy, H. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2097 · Cited by 655
The development of the subplate and thalamocortical connections in the human foetal brain
Kostović, I., & Judaš, M. (2010) · Acta Paediatrica · doi:10.1111/j.1651-2227.2010.01811.x · Cited by 462
Self-citationThe subplate and early cortical circuits
Kanold, P. O., & Luhmann, H. J. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153244 · Cited by 440
Schizophrenia: a tale of two critical periods for prefrontal cortical development
Selemon, L. D., & Zecevic, N. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.115 · Cited by 336
G1 Phase Regulation, Area-Specific Cell Cycle Control, and Cytoarchitectonics in the Primate Cortex
Lukaszewicz, A., Savatier, P., Cortay, V., Giroud, P., Huissoud, C., Berland, M., Kennedy, H., & Dehay, C. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.032 · Cited by 315
Oligodendrocyte development and the onset of myelination in the human fetal brain
Jakovcevski, I. (2009) · Frontiers in Neuroanatomy · doi:10.3389/neuro.05.005.2009 · Cited by 323
Entry and distribution of microglial cells in human embryonic and fetal cerebral cortex
Monier, A., Adle-Biassette, H., Delezoide, A.-L., Evrard, P., Gressens, P., & Verney, C. (2007) · Journal of Neuropathology and Experimental Neurology · doi:10.1097/nen.0b013e3180517b46 · Cited by 291
Cortical development: View from neurological mutants two decades later
Rakic, P., & Caviness, V. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90258-9 · Cited by 287
Self-citationMarín‐Padilla, M. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903210205 · Cited by 285
Transient cortical circuits match spontaneous and sensory-driven activity during development
Molnár, Z., Luhmann, H. J., & Kanold, P. O. (2020) · Science · doi:10.1126/science.abb2153 · Cited by 280
Kwan, K. Y., Lam, M. M. S., Krsnik, Ž., Kawasawa, Y. I., Lefebvre, V., & Šestan, N. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0806791105 · Cited by 271
Contributions of cortical subventricular zone to the development of the human cerebral cortex
Zecevic, N., Chen, Y., & Filipovic, R. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20714 · Cited by 269
Chapter 9 Neuronal development in human prefrontal cortex in prenatal and postnatal stages
Mrzljak, L., Uylings, H. B. M., Van Eden, G. G., & Judáš, M. (1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62681-3 · Cited by 247
Simms, M. L., Kemper, T. L., Timbie, C. M., Bauman, M. L., & Blatt, G. J. (2009) · Acta Neuropathologica · doi:10.1007/s00401-009-0568-2 · Cited by 183
Exploring early human brain development with structural and physiological neuroimaging
Vasung, L., Abaci Turk, E., Ferradal, S. L., Sutin, J., Stout, J. N., Ahtam, B., Lin, P.-Y., & Grant, P. E. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2018.07.041 · Cited by 177
Vasung, L., Huang, H., Jovanov‐Milošević, N., Pletikos, M., Mori, S., & Kostović, I. (2010) · Journal of Anatomy · doi:10.1111/j.1469-7580.2010.01260.x · Cited by 169
Exploring the Early Organization and Maturation of Linguistic Pathways in the Human Infant Brain
Dubois, J., Poupon, C., Thirion, B., Simonnet, H., Kulikova, S., Leroy, F., Hertz-Pannier, L., & Dehaene-Lambertz, G. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv082 · Cited by 165
In vitro MRI of brain development
Radoš, M., Judaš, M., & Kostović, I. (2006) · European Journal of Radiology · doi:10.1016/j.ejrad.2005.11.019 · Cited by 152
Zecevic, N., & Verney, C. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903510404 · Cited by 149
Ontogenesis of goal-directed behavior: anatomo-functional considerations
Kostović, I., Judaš, M., Petanjek, Z., & Šimić, G. (1995) · International Journal of Psychophysiology · doi:10.1016/0167-8760(94)00081-o · Cited by 139
Species-dependent posttranscriptional regulation of NOS1 by FMRP in the developing cerebral cortex
Kwan, K. Y., Lam, M. M. S., Johnson, M. B., Dube, U., Shim, S., Rašin, M.-R., Sousa, A. M. M., Fertuzinhos, S., Chen, J.-G., Arellano, J. I., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.060 · Cited by 137
Self-citationDifferential survival of Cajal-Retzius cells in organotypic cultures of hippocampus and neocortex
Del Rı́o, J. A., Heimrich, B., Supèr, H., Borrell, V., Frotscher, M., & Soriano, E. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-21-06896.1996 · Cited by 133
Sestan, N., & State, M. W. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.015 · Cited by 127
Kostović, I. (1991) · Progress in Brain Research · doi:10.1016/s0079-6123(08)62682-5 · Cited by 127
Self-citationGrowth trajectories of the human fetal brain tissues estimated from 3D reconstructed in utero MRI
Scott, J. A., Habas, P. A., Kim, K., Rajagopalan, V., Hamzelou, K. S., Corbett‐Detig, J. M., Barkovich, A. J., Glenn, O. A., & Studholme, C. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.04.001 · Cited by 119
Verney, C., Lebrand, C., & Gaspar, P. (2002) · The Anatomical Record · doi:10.1002/ar.10089 · Cited by 119
Early human brain development: Starring the subplate
Hadders-Algra, M. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.06.017 · Cited by 100
Samuelsen, G. B. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.2.115 · Cited by 95
Transcriptomic Perspectives on Neocortical Structure, Development, Evolution, and Disease
Lein, E. S., Belgard, T. G., Hawrylycz, M., & Molnár, Z. (2017) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-070815-013858 · Cited by 92
In search of common developmental and evolutionary origin of the claustrum and subplate
Bruguier, H., Suarez, R., Manger, P., Hoerder‐Suabedissen, A., Shelton, A. M., Oliver, D. K., Packer, A. M., Ferran, J. L., García‐Moreno, F., Puelles, L., et al. (2020) · Journal of Comparative Neurology · doi:10.1002/cne.24922 · Cited by 84
Spatio-temporal extension in site of origin for cortical calretinin neurons in primates
Hladnik, A., Džaja, D., Darmopil, S., Jovanov-MiloÅ¡ević, N., & Petanjek, Z. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00050 · Cited by 72
Total number of cells in the human newborn telencephalic wall
Larsen, C. C., Bonde Larsen, K., Bogdanovic, N., Laursen, H., Græm, N., Badsberg Samuelsen, G., & Pakkenberg, B. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.01.005 · Cited by 79
Comparative Aspects of Subplate Zone Studied with Gene Expression in Sauropsids and Mammals
Wang, W. Z., Oeschger, F. M., Montiel, J. F., García-Moreno, F., Hoerder-Suabedissen, A., Krubitzer, L., Ek, C. J., Saunders, N. R., Reim, K., Villalón, A., et al. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq278 · Cited by 76
Hypothesis on the Dual Origin of the Mammalian Subplate
Montiel, J. F., Wang, W. Z., Oeschger, F. M., Hoerder-Suabedissen, A., Tung, W. L., García-Moreno, F., Holm, I. E., Villalón, A., & Molnár, Z. (2011) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2011.00025 · Cited by 70
Human fetal brain connectome: structural network development from middle fetal stage to birth
Song, L., Mishra, V., Ouyang, M., Peng, Q., Slinger, M., Liu, S., & Huang, H. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00561 · Cited by 71
Lessons from infant learning for unsupervised machine learning
Zaadnoordijk, L., Besold, T. R., & Cusack, R. (2022) · Nature Machine Intelligence · doi:10.1038/s42256-022-00488-2 · Cited by 65
Ip, B. K., Bayatti, N., Howard, N. J., Lindsay, S., & Clowry, G. J. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq219 · Cited by 58
Dubois, J., Adibpour, P., Poupon, C., Hertz-Pannier, L., & Dehaene-Lambertz, G. (2016) · Brain Plasticity · doi:10.3233/bpl-160031 · Cited by 40
Development of the Cell Population in the Brain White Matter of Young Children
Sigaard, R. K., Kjær, M., & Pakkenberg, B. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhu178 · Cited by 43
Global Network Organization of the Fetal Functional Connectome
De Asis-Cruz, J., Andersen, N., Kapse, K., Khrisnamurthy, D., Quistorff, J., Lopez, C., Vezina, G., & Limperopoulos, C. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhaa410 · Cited by 40
Exploiting human anatomical variability as a link between genome and cognome
Leonard, C. M., Eckert, M. A., & Kuldau, J. M. (2006) · Genes, Brain and Behavior · doi:10.1111/j.1601-183x.2006.00196.x · Cited by 38
Concurrent Generation of Subplate and Cortical Plate Neurons in Developing Trisomy 16 Mouse Cortex
Cheng, A., Haydar, T. F., Yarowsky, P. J., & Krueger, B. K. (2004) · Developmental Neuroscience · doi:10.1159/000082142 · Cited by 22
Metadata
- Authors
- Kostovic, I., & Rakic, P.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1990-07-15
- Volume
- 297
- Issue
- 3
- Pages
- 441-470
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2077552569
- Cited by
- 913
- References
- 7
- FWCI
- 7.55
- Type
- journal article
- Language
- en
- Open access
- closed
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