Literature DB >> 2376772

Axon overproduction and elimination in the corpus callosum of the developing rhesus monkey.

A S LaMantia1, P Rakic.   

Abstract

We have studied the cytological and quantitative aspects of axon addition and elimination in the corpus callosum of the developing rhesus monkey. Electron microscopic analysis reveals that during fetal development the number of callosal axons increases from 4 million at embryonic day 65 (E65) to 188 million at birth (E 165). Thus, the number of callosal axons in newborn monkeys exceeds the number present in the adult (an average of 56 million; LaMantia and Rakic, 1990a) by at least 3.5 times. Although there is some variability among the 11 fetal and newborn monkeys examined, there appears to be a progressive increase in the total number of callosal axons from midgestation through birth. The presence and numbers of growth cones from E65 through birth suggests that axon addition occurs exclusively during this period. There is no ultrastructural or quantitative indication of postnatal axon addition. After birth, about 70% of the axons in the callosum are eliminated in 2 phases. During the first phase, which includes the first 3 postnatal weeks, approximately 80 million axons are lost at an estimated rate of 4.4 million/d or 50/sec. During the second phase, which continues for the following 3 months, an additional 50 million axons are eliminated at a rate of 0.5 million/d or 5/sec until the adult value is reached. A discontinuous distribution of different classes of axons along the anterior-posterior axis of the tract reminiscent of the pattern seen in the adult is detectable before the onset of the first phase of axon elimination. Since the basic topography and terminal field patterns of callosal projections are well established before birth in all regions of the monkey cortex examined so far (Goldman-Rakic et al., 1983; Killackey and Chalupa, 1986; Dehay et al., 1988; Schwartz and Goldman-Rakic, 1990), we conclude that the massive postnatal elimination of callosal axons described here is unlikely to play a significant role in the development of discretely patterned callosal projection zones or their columnar terminations. The coincidence of axon elimination and the increase in synaptic density throughout the primate cerebral cortex during the first 6 postnatal months (Rakic et al., 1986), however, suggests that supernumerary axons may be lost during a process that results in the local proliferation of synapses from a subset of initial interhemispheric projections.

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Year:  1990        PMID: 2376772      PMCID: PMC6570389     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  134 in total

1.  Microstructural development: organizational differences of the fiber architecture between children and adults in dorsal and ventral visual streams.

Authors:  Thomas Loenneker; Peter Klaver; Kerstin Bucher; Janine Lichtensteiger; Adrian Imfeld; Ernst Martin
Journal:  Hum Brain Mapp       Date:  2010-06-09       Impact factor: 5.038

2.  The corpus callosum in primates: processing speed of axons and the evolution of hemispheric asymmetry.

Authors:  Kimberley A Phillips; Cheryl D Stimpson; Jeroen B Smaers; Mary Ann Raghanti; Bob Jacobs; Anastas Popratiloff; Patrick R Hof; Chet C Sherwood
Journal:  Proc Biol Sci       Date:  2015-11-07       Impact factor: 5.349

3.  Early phenotype expression of cortical neurons: evidence that a subclass of migrating neurons have callosal axons.

Authors:  M L Schwartz; P Rakic; P S Goldman-Rakic
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-15       Impact factor: 11.205

4.  The development of corpus callosum microstructure and associations with bimanual task performance in healthy adolescents.

Authors:  Ryan L Muetzel; Paul F Collins; Bryon A Mueller; Ann M Schissel; Kelvin O Lim; Monica Luciana
Journal:  Neuroimage       Date:  2007-10-25       Impact factor: 6.556

Review 5.  The radial edifice of cortical architecture: from neuronal silhouettes to genetic engineering.

Authors:  Pasko Rakic
Journal:  Brain Res Rev       Date:  2007-03-31

6.  Development of human brain structural networks through infancy and childhood.

Authors:  Hao Huang; Ni Shu; Virendra Mishra; Tina Jeon; Lina Chalak; Zhiyue J Wang; Nancy Rollins; Gaolang Gong; Hua Cheng; Yun Peng; Qi Dong; Yong He
Journal:  Cereb Cortex       Date:  2013-12-11       Impact factor: 5.357

Review 7.  LTD-like molecular pathways in developmental synaptic pruning.

Authors:  Claire Piochon; Masanobu Kano; Christian Hansel
Journal:  Nat Neurosci       Date:  2016-09-27       Impact factor: 24.884

8.  Asymmetry of White Matter Pathways in Developing Human Brains.

Authors:  Jae W Song; Paul D Mitchell; James Kolasinski; P Ellen Grant; Albert M Galaburda; Emi Takahashi
Journal:  Cereb Cortex       Date:  2014-05-08       Impact factor: 5.357

9.  Cognitive control and white matter callosal microstructure in methamphetamine-dependent subjects: a diffusion tensor imaging study.

Authors:  Ruth Salo; Thomas E Nordahl; Michael H Buonocore; Yutaka Natsuaki; Christy Waters; Charles D Moore; Gantt P Galloway; Martin H Leamon
Journal:  Biol Psychiatry       Date:  2008-09-23       Impact factor: 13.382

10.  Normal centrolineal myelination of the callosal splenium reflects the development of the cortical origin and size of its commissural fibers.

Authors:  Matthew T Whitehead; Anand Raju; Asim F Choudhri
Journal:  Neuroradiology       Date:  2014-01-26       Impact factor: 2.804

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