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AuthorAzevedo, Leonardo C. de
AuthorPereira, Cecilia Hedin
AuthorLent, Roberto
Access date2013-02-20T17:14:42Z
Available date2013-02-20T17:14:42Z
Document date1997
CitationAZEVEDO, Leonardo C. de; HEIDIN-PEREIRA, Cecília; LENT, Roberto. Callosal neurons in the cingulate cortical plate and subplate of human fetuses. The Journal of Comparative Neurology, New York, v. 386, n.1, p. 60-70, Sept. 1997.pt_BR
ISSN0021-9967
URIhttps://www.arca.fiocruz.br/handle/icict/6321
SponsorshipFINEPpt_BR
Languageengpt_BR
PublisherWiley-Lisspt_BR
xmlui.metadata.dc.relation.isbasedonAboitiz, F., A.B. Scheibel, R.S. Fisher, and E. Zaidel (1992) Fiber composition of the human corpus callosum. Brain Res. 598:143–153.pt_BR
xmlui.metadata.dc.relation.isbasedonAggoun-Zouaoui, D., and G.M. Innocenti (1994) Juvenile visual callosal axons in kittens display origin- and fate-related morphology and distribution of arbors. Eur. J. Neurosci. 6:1846–1863.pt_BR
xmlui.metadata.dc.relation.isbasedonAntonini, A., and C.J. Shatz (1990) Relation between putative transmitter phenotypes and connectivity of subplate neurons during cerebral cortex development. Eur. J. Neurosci. 2:744–761.pt_BR
xmlui.metadata.dc.relation.isbasedonAuladell, C., A. Martinez, S. Alcantara, H. Supe`r, and E. Soriano (1995) Migrating neurons in the developing cerebral cortex of the mouse send callosal axons. Neuroscience 64:1091–1103.pt_BR
xmlui.metadata.dc.relation.isbasedonBecker, L.E., D.L. Armstrong, F. Chan, and M.M. Wood (1984) Dendritic development in human occipital cortical neurons. Dev. Brain Res. 13:117–124.pt_BR
xmlui.metadata.dc.relation.isbasedonBerbel, P., and G.M. Innocenti (1988) The development of the corpus callosum in cats: A light- and electron-microscopic study. J. Comp. Neurol. 276:132–156.pt_BR
xmlui.metadata.dc.relation.isbasedonChalupa, L.M., and H.P. Killackey (1989) Process elimination underlies ontogenetic change in the distribution of callosal projection neurons in the postcentral gyrus of the fetal rhesus monkey. Proc. Natl. Acad. Sci. USA86:1076–1079.pt_BR
xmlui.metadata.dc.relation.isbasedonChow, K.L., H.D. Baumbach, and R. Lawson (1981) Callosal projections of the striate cortex in the neonatal rabbit. Exp. Brain Res. 42:122–126.pt_BR
xmlui.metadata.dc.relation.isbasedonChun, J.J.M., M.J. Nakamura, and C.J. Shatz (1987) Transient cells of the developing mammalian telencephalon are peptide immunoreactive neurons. Nature 325:617–620.pt_BR
xmlui.metadata.dc.relation.isbasedonCode, R.A., and J.A. Winer (1985) Commissural neurons in layer III of cat primary auditory cortex (AI): Pyramidal and non-pyramidal cell input. J. Comp. Neurol. 242:485–510.pt_BR
xmlui.metadata.dc.relation.isbasedondeAzevedo, L.C., R. Lent, and C. Hedin-Pereira (1995) Callosal neurons and glial cells in the developing cerebral cortex of human fetuses. Neurosci. Abstr. 21:2021.pt_BR
xmlui.metadata.dc.relation.isbasedondeAzevedo, L.C., M.M. Rocha, C. Hedin-Pereira, J.G. Franca, and R. Lent (1996) The emergence of NADPH-diaphorase-positive neurons in the cortical subplate of human fetuses. Neurosci. Abstr. 22:1973.pt_BR
xmlui.metadata.dc.relation.isbasedonDe Carlos, J.A., and D.D.M. O’Leary (1992) Growth and targeting of subplate axons and establishment of major cortical pathways. J. Neurosci. 12:1194–1211.pt_BR
xmlui.metadata.dc.relation.isbasedonDiao, Y-C., and K-F. So (1991) Dendritic morphology of visual callosal neurons in the golden hamster. Brain Behav. Evol. 37:1–9.pt_BR
xmlui.metadata.dc.relation.isbasedonDursteler, M.R., C. Blakemore, and L.J. Garey (1979) Projections to the visual cortex in the golden hamster. J. Comp. Neurol. 183:185–204.pt_BR
xmlui.metadata.dc.relation.isbasedonGames, K.D., and J.A. Winer (1988) Layer V in rat auditory cortex: projections to the inferior colliculus and contralateral cortex. Hearing Res. 34:1–26.pt_BR
xmlui.metadata.dc.relation.isbasedonGodement, P., J. Vanselow, S. Thanos, and F. Bonhoeffer (1987) A study of developing visual systems with a new method of staining neurones and their processes in fixed tissue. Development 101:697–713.pt_BR
xmlui.metadata.dc.relation.isbasedonHallman, L.E., B.R. Schofield, and C-S. Lin (1988) Dendritic morphology and axon collaterals of corticotectal, corticopontine, and callosal neurons in layer V of primary visual cortex of the hooded rat. J. Comp. Neurol. 272:149–160.pt_BR
xmlui.metadata.dc.relation.isbasedonHonig, M.G., and R.I. Hume (1989) Dil and DiO: Versatile fluorescent dyes for neuronal labelling and pathway tracing. Trends Neurosci. 12:333– 341.pt_BR
xmlui.metadata.dc.relation.isbasedonHu¨ bener, M., and J. Bolz (1988) Morphology of identified projection neurons in layer V of rat visual cortex. Neurosci. Lett. 94:76–81.pt_BR
xmlui.metadata.dc.relation.isbasedonHughes, C.M., and A. Peters (1990) Morphological evidence for callosally projecting nonpyramidal neurons in rat visual cortex. Anat. Embryol. 182:591–604.pt_BR
xmlui.metadata.dc.relation.isbasedonInnocenti, G.M. (1981) Growth and reshaping of axons in the establishment of visual callosal connections. Science 212:824–827.pt_BR
xmlui.metadata.dc.relation.isbasedonInnocenti, G.M., and R. Caminiti (1980) Postnatal shaping of callosal connections from sensory areas. Exp. Brain Res. 38:381–394.pt_BR
xmlui.metadata.dc.relation.isbasedonInnocenti, G.M., and S.K. Clarke (1984) The organization of immature callosal connections. J. Comp. Neurol. 230:287–309.pt_BR
xmlui.metadata.dc.relation.isbasedonInnocenti, G.M., L. Fiore, and R. Caminiti (1977) Exuberant projection into the corpus callosum from the visual cortex of newborn cats. Neurosci. Lett. 4:237–242.pt_BR
xmlui.metadata.dc.relation.isbasedonIvy, G.O., and H.P. Killackey (1981) The ontogeny of the distribution of callosal projection neurons in the rat parietal cortex. J. Comp. Neurol. 195:367–389.pt_BR
xmlui.metadata.dc.relation.isbasedonJacobson, S., and J.Q. Trojanowski (1974) The cells of origin of the corpus callosum in rat, cat, and rhesus monkey. Brain Res. 74:149–155.pt_BR
xmlui.metadata.dc.relation.isbasedonJouandet, M.L., L.J. Garey, and H-P. Lipp (1984) Distribution of the cells of origin of the corpus callosum and anterior commissure in the marmoset monkey. Anat. Embryol. 169:45–59.pt_BR
xmlui.metadata.dc.relation.isbasedonKillackey, H.P., and L.M. Chalupa (1986) Ontogenetic change in the distribution of callosal projection neurons in the postcentral gyrus of the fetal rhesus monkey. J. Comp. Neurol. 244:331–348.pt_BR
xmlui.metadata.dc.relation.isbasedonKoenderink, M.J.Th., H.B.M. Uylings, and L. Mrzljak (1994) Postnatal maturation of the layer III pyramidal neurons in the human prefrontal cortex:Aquantitative Golgi analysis. Brain Res. 653:173–182.pt_BR
xmlui.metadata.dc.relation.isbasedonKoenderink, M.J.Th., and H.B.M. Uylings (1995) Postnatal maturation of layer V pyramidal neurons in the human prefrontal cortex: A quantitative Golgi analysis. Brain Res. 678:233–243.pt_BR
xmlui.metadata.dc.relation.isbasedonKoester, S.E., and D.D.M. O’Leary (1992) Functional classes of cortical projection neurons develop dendritic distinctions by class-specific sculpting of an early common pattern. J. Neurosci. 12:1382–1393.pt_BR
xmlui.metadata.dc.relation.isbasedonKoester, S.E., and D.D.M. O’Leary (1994) Axons of early generated neurons in cingulate cortex pioneer the corpus callosum. J. Neurosci. 14:6608– 6620.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I. (1990) Structural and histochemical reorganization of the human prefrontal cortex during perinatal and postnatal life. Progr. Brain Res. 85:223–240.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I., and P.S. Goldman-Rakic (1983) Transient cholinesterase staining in the mediodorsal nucleus of the thalamus and its connections in the developing human and monkey brain. J. Comp. Neurol. 219:431– 447.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I., and J. Krmpotic (1976) Early prenatal ontogenesis of the neuronal connections in the interhemispheric cortex of the human gyrus cinguli. Verh. Anat. Ges. 70:305–316.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I., and P. Rakic (1984) Development of prestriate visual projections in the monkey and human fetal cerebrum revealed by transient cholinesterase staining. J. Neurosci. 4:25–42.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I., and P. Rakic (1990) Developmental history of the transient subplate zone in the visual and somatosensory cortex of the macaque monkey and human brain. J. Comp. Neurol. 297:441–470.pt_BR
xmlui.metadata.dc.relation.isbasedonKostovic, I., J. Skavic, and D. Strinovic (1988) Acetylcholinesterase in the human frontal associative cortex during the period of cognitive development: Early laminar shifts and late innervation of pyramidal neurons. Neurosci. Lett. 90:107–112.pt_BR
xmlui.metadata.dc.relation.isbasedonKrmpotic-Nemanic, J., I. Kostovic, Z. Kelovic, and D. Nemanic (1980) Development of acetylcholinesterase (AChE) staining in human fetal auditory cortex. Acta Otolaryngol. 89:388–392.pt_BR
xmlui.metadata.dc.relation.isbasedonKrmpotic-Nemanic, J., I. Kostovic, Z. Kelovic, D. Nemanic, and L. Mrzljak (1983) Development of the human fetal auditory cortex: Growth of afferent fibers. Acta Anat. 116:69–73.pt_BR
xmlui.metadata.dc.relation.isbasedonLaMantia, A.S., and P. Rakic (1990) Axon overproduction and elimination in the corpus callosum of the developing Rhesus monkey. J. Neurosci. 10:2156–2175.pt_BR
xmlui.metadata.dc.relation.isbasedonLent, R., C. Hedin-Pereira, J.R.L. Menezes, and S. Jhaveri (1990) Neurogenesis and development of callosal and intracortical connections in the hamster. Neuroscience 38:21–37.pt_BR
xmlui.metadata.dc.relation.isbasedonLent, R., L. deAzevedo, and C. Hedin-Pereira (1995) Callosally-projecting subplate cells in fetal human brains. Neurosci. Abstr. 21:2021.pt_BR
xmlui.metadata.dc.relation.isbasedonMarin-Padilla, M. (1969) Origin of the pericellular baskets of the pyramidal cells of the human motor cortex:AGolgi study. Brain Res. 14:633–646.pt_BR
xmlui.metadata.dc.relation.isbasedonMarin-Padilla, M. (1970a) Prenatal and early postnatal ontogenesis of the human motor cortex: a Golgi study. I. The prenatal sequential development of the cortical layers. Brain Res. 23:167–183.pt_BR
xmlui.metadata.dc.relation.isbasedonMarin-Padilla, M. (1970b) Prenatal and early postnatal ontogenesis of the human motor cortex: A Golgi study. II. The basket-pyramidal cell system. Brain Res. 23:185–191.pt_BR
xmlui.metadata.dc.relation.isbasedonMarin-Padilla, M. (1992) Ontogenesis of the pyramidal cell of the mammalian neocortex and developmental cytoarchitectonics: A unifying theory. J. Comp. Neurol. 321:223–240.pt_BR
xmlui.metadata.dc.relation.isbasedonMcConnell, S.K., A. Ghosh, and C.J. Shatz (1989) Subplate neurons pioneer the first axon pathway from the cerebral cortex. Science 245:978–982.pt_BR
xmlui.metadata.dc.relation.isbasedonMrzljak, L., H.B.M. Uylings, I. Kostovic, and C.G. Van Eden (1988) Prenatal development of neurons in the human prefrontal cortex. I. A qualitative Golgi study. J. Comp. Neurol. 271:355–386.pt_BR
xmlui.metadata.dc.relation.isbasedonMrzljak, L., H.B.M. Uylings, C.G. Van Eden, and M. Juda´s (1990) Neuronal development in human prefrontal cortex in prenatal and postnatal stages. Prog. Brain Res. 85:185–222.pt_BR
xmlui.metadata.dc.relation.isbasedonMrzljak, L., H.B.M. Uylings, I. Kostovic, and C.G. Van Eden (1992) Prenatal development of neurons in the human prefrontal cortex. II. A quantitative Golgi study. J. Comp. Neurol. 316:485–496.pt_BR
xmlui.metadata.dc.relation.isbasedonO’Leary, D.D.M., B.B. Stanfield, and W.M. Cowan (1981) Evidence that the early postnatal restriction of the cells of origin of the callosal projection is due to the elimination of axonal collaterals rather than to the death of neurons. Dev. Brain Res. 1:607–617.pt_BR
xmlui.metadata.dc.relation.isbasedonPerry, E.K., C.J. Smith, J.R. Atack, J.M. Candy,M. Johnson, and R.H. Perry (1986) Neocortical cholinergic enzyme and receptor activities in the human fetal brain. J. Neurochem. 47:1262–1269.pt_BR
xmlui.metadata.dc.relation.isbasedonPeters, A., B.R. Payne, and K. Josephson (1990) Transcallosal nonpyramidal cell projections from visual cortex in the cat. J. Comp. Neurol. 302:124–142.pt_BR
xmlui.metadata.dc.relation.isbasedonPurpura, D.P. (1975) Dendritic differentiation in human cerebral cortex: Normal and aberrant developmental patterns. In G.W. Kreutzberg (ed): DEVELOPING CALLOSAL NEURONS IN HUMANS 69 Physiology and Pathology of Dendrites. Advances in Neurology, Vol. 12. New York: Raven Press, pp. 91–116.pt_BR
xmlui.metadata.dc.relation.isbasedonRakic, P., and P.I. Yakovlev (1968) Development of the corpus callosum and cavum septi in man. J. Comp. Neurol. 132:45–72.pt_BR
xmlui.metadata.dc.relation.isbasedonSchwartz, M.L., P. Rakic, and P.S. Goldman-Rakic (1991) Early phenotype expression of cortical neurons: Evidence that a subclass of migrating neurons have callosal axons. Proc. Natl. Acad. Sci. USA 88:1354–1358.pt_BR
xmlui.metadata.dc.relation.isbasedonSegraves, M.A., and A.C. Rosenquist (1982) The distribution of the cells of origin of callosal projections in cat visual cortex. J. Neurosci. 2:1079– 1089.pt_BR
xmlui.metadata.dc.relation.isbasedonSripanidkulchai, K., and J.M. Wyss (1987) The laminar organization of efferent neuronal bodies in the retrosplenial granular cortex. Brain Res. 406:255–269.pt_BR
xmlui.metadata.dc.relation.isbasedonVan Essen, D.C., W.T. Newsome, and J.L. Bixby (1982) The pattern of interhemispheric connections and its relationships to extrastriate visual areas in the macaque monkey. J. Neurosci. 2:265–283.pt_BR
xmlui.metadata.dc.relation.isbasedonVercelli, A., F. Assal, and G.M. Innocenti (1992) Emergence of callosallyprojecting neurons with stellate morphology in the visual cortex of the kitten. Exp. Brain Res. 90:346–358.pt_BR
xmlui.metadata.dc.relation.isbasedonWise, S.P., and E.G. Jones (1976) The organization and postnatal development of the commissural projection of the rat somatic sensory cortex. J. Comp. Neurol. 168:313–343.pt_BR
xmlui.metadata.dc.relation.isbasedonYorke, C.H., and V.S. Caviness (1975) Interhemispheric neocortical connections of the corpus callosum in the normal mouse: A study based on anterograde and retrograde methods. J. Comp. Neurol. 164: 233–246.pt_BR
Rightsrestricted access
TitleCallosal neurons in the cingulate cortical plate and subplate of human fetusespt_BR
TypeArticle
DOI10.1002/(SICI)1096-9861(19970915)386:1<60::AID-CNE7>3.0.CO;2-B
AbstractGiven the scarcity of data on the development of the cerebral cortex and its connections in man, four brains of human fetuses at 25, 26, 30, and 32 weeks postovulation were used to investigate the following: 1) the radial distribution of callosal neurons in the cingulate cortex at the immediate postmigratory period; 2) the existence of callosally projecting neurons in the cortical subplate; and 3) the dendritic morphology of developing callosal neurons. The carbocyanine dye (1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate) (DiI) was used as a fluorescent postmortem tracer for the identification and morphological description of callosal neurons, 4-6 months after the insertion of DiI crystals at the callosal midplane. Sixty-one completely labeled neurons were selected for microscopical analysis, drawn by use of a camera lucida and photographed. The main findings were the following: 1) the human cingulate cortex at 25-32 weeks postovulation contains callosally projecting neurons both in the cortical plate and in the subplate; 2) callosal cells in the plate are mostly spiny pyramids with somata distributed uniformly throughout the depth of the plate, irrespective of rostrocaudal position. They have well-differentiated basal dendrites and apical dendrites that consistently ramify within layer 1; 3) subplate callosal cells are smooth neurons of diverse dendritic morphology, distributed widely throughout the subplate depth. They were classified into four cell types according to the dendritic morphology: radially oriented, horizontally oriented, multipolars, and inverted pyramids. These findings extend to the human brain some of the evidence obtained in animals concerning the development of the cerebral cortex, especially those that are relevant to the formation of a transitory circuitry in the subplate.pt_BR
AffilliationFundação Oswaldo Cruz. Instituto Fernandes Figueira. Rio de Janeiro, RJ, Brasil / Universidade Federal do Rio de Janeiro. Instituto de Ciências Biomédicas. Departamento de Anatomia. Rio de Janeiro, RJ, Brasil.pt_BR
SubjectCorpus Callosumpt_BR
SubjectCortical Developmentpt_BR
SubjectLimbic Systempt_BR
SubjectInterhemispheric Connectionspt_BR
SubjectHuman Brainpt_BR
DeCSCórtex Cerebralpt_BR
DeCSCorpo Calosopt_BR
DeCSFetopt_BR
DeCSGiro do Cíngulopt_BR
Embargo date2030-12-31


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