Literature DB >> 1500541

Ontogenesis of the pyramidal cell of the mammalian neocortex and developmental cytoarchitectonics: a unifying theory.

M Marín-Padilla1.   

Abstract

The prenatal development of the mammalian neocortex has been analyzed, with the rapid Golgi method, in a variety of experimental animals (hamster, mouse, rat, and cat) and in humans. A new developmental conception of the structural organization of the mammalian neocortex is discussed. Neocortical development begins with the establishment of the primordial plexiform layer (PPL) which precedes and is a prerequisite for the subsequent formation of the cortical plate (CP). The formation of the CP occurs, in its entirety, within the PPL. During its development, three fundamental neuronal events occur: migration, early differentiation, and late maturation. All migrating neurons, travelling on radial glial fibers, reach layer I, develop an apical dendrite, and establish contacts with its elements. These newly differentiated neurons assume similar morphology resembling embryonic pyramidal cells. As such, an early differentiation stage common to all neurons of the CP is established. During the late maturation stage, all CP neurons acquire their specific phenotypic structural and functional features. Only pyramidal neurons retain and expand their original connections with layer I while other neuronal types lose these connections. The pyramidal cell is redefined in developmental terms: the neocortex's pyramidal cell is both structurally and functionally locked into position between layer I and the cortical depth of its soma. During mammalian evolution pyramidal cells are forced to structurally and functionally elongate their apical dendrite outwardly to accommodate an increasing amount of information without losing either their original anchorage to layer I or their cortical depth. This unique property of pyramidal neurons is considered to be a mammalian innovation. Based on these observations, a unifying developmental cytoarchitectonic theory applicable to all mammals is proposed. The theory considers the CP to be a mammalian innovation and to represent a single, stratified, and expanding telencephalic nucleus. The theory envisions the mammalian neocortex as an open biological system capable of progressive expansion by the recruitment and transformation of primitive neurons from upper layer II into pyramidal cells. Hence, the number of pyramidal cell strata increases over the course of mammalian phylogeny. The developmental roles of layer I in the migration of neurons, formation of the CP, unique morphology of pyramidal cells, and overall structural organization of the mammalian neocortex are emphasized.

Entities:  

Mesh:

Year:  1992        PMID: 1500541     DOI: 10.1002/cne.903210205

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  58 in total

1.  The establishment of GABAergic and glutamatergic synapses on CA1 pyramidal neurons is sequential and correlates with the development of the apical dendrite.

Authors:  R Tyzio; A Represa; I Jorquera; Y Ben-Ari; H Gozlan; L Aniksztejn
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Formation and structural organization of the barrier on the outer surface of the brain.

Authors:  V A Otellin; D E Korzhevskii
Journal:  Neurosci Behav Physiol       Date:  2004-05

Review 3.  Neurons of layer I and their significance in the embryogenesis of the neocortex.

Authors:  V E Okhotin; S G Kalinichenko
Journal:  Neurosci Behav Physiol       Date:  2004-01

4.  Developing neocortex organization and connectivity in cats revealed by direct correlation of diffusion tractography and histology.

Authors:  Emi Takahashi; Guangping Dai; Glenn D Rosen; Ruopeng Wang; Kenichi Ohki; Rebecca D Folkerth; Albert M Galaburda; Van J Wedeen; P Ellen Grant
Journal:  Cereb Cortex       Date:  2010-05-21       Impact factor: 5.357

5.  The cerebral cortex overlying periventricular leukomalacia: analysis of pyramidal neurons.

Authors:  Sarah E Andiman; Robin L Haynes; Felicia L Trachtenberg; Saraid S Billiards; Rebecca D Folkerth; Joseph J Volpe; Hannah C Kinney
Journal:  Brain Pathol       Date:  2010-02-08       Impact factor: 6.508

6.  Developmental changes and injury induced disruption of the radial organization of the cortex in the immature rat brain revealed by in vivo diffusion tensor MRI.

Authors:  Stéphane V Sizonenko; Emily J Camm; Joel R Garbow; Stephan E Maier; Terrie E Inder; Chris E Williams; Jeffrey J Neil; Petra S Huppi
Journal:  Cereb Cortex       Date:  2007-01-27       Impact factor: 5.357

7.  Association of impaired neuronal migration with cognitive deficits in extremely preterm infants.

Authors:  Ken-Ichiro Kubo; Kimiko Deguchi; Taku Nagai; Yukiko Ito; Keitaro Yoshida; Toshihiro Endo; Seico Benner; Wei Shan; Ayako Kitazawa; Michihiko Aramaki; Kazuhiro Ishii; Minkyung Shin; Yuki Matsunaga; Kanehiro Hayashi; Masaki Kakeyama; Chiharu Tohyama; Kenji F Tanaka; Kohichi Tanaka; Sachio Takashima; Masahiro Nakayama; Masayuki Itoh; Yukio Hirata; Barbara Antalffy; Dawna D Armstrong; Kiyofumi Yamada; Ken Inoue; Kazunori Nakajima
Journal:  JCI Insight       Date:  2017-05-18

8.  Developmental Trajectories for Visuo-Spatial Attention are Altered by Prenatal Alcohol Exposure: A Longitudinal FMRI Study.

Authors:  P Gautam; S C Nuñez; K L Narr; S N Mattson; P A May; C M Adnams; E P Riley; K L Jones; E C Kan; E R Sowell
Journal:  Cereb Cortex       Date:  2014-08-04       Impact factor: 5.357

Review 9.  Nitric oxide signaling in the development and evolution of language and cognitive circuits.

Authors:  Owen H Funk; Kenneth Y Kwan
Journal:  Neurosci Res       Date:  2014-06-13       Impact factor: 3.304

10.  Surface based analysis of diffusion orientation for identifying architectonic domains in the in vivo human cortex.

Authors:  Jennifer A McNab; Jonathan R Polimeni; Ruopeng Wang; Jean C Augustinack; Kyoko Fujimoto; Allison Stevens; Christina Triantafyllou; Thomas Janssens; Reza Farivar; Rebecca D Folkerth; Wim Vanduffel; Lawrence L Wald
Journal:  Neuroimage       Date:  2012-12-16       Impact factor: 6.556

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