Literature DB >> 21629587

Synchronized changes to relative neuron populations in postnatal human neocortical development.

David L Cooper, James E Gentle, Ernest Barreto, James L Olds.   

Abstract

UNLABELLED: Mammalian prenatal neocortical development is dominated by the synchronized formation of the laminae and migration of neurons. Postnatal development likewise contains "sensitive periods" during which functions such as ocular dominance emerge. Here we introduce a novel neuroinformatics approach to identify and study these periods of active development. Although many aspects of the approach can be used in other studies, some specific techniques were chosen because of a legacy dataset of human histological data (Conel in The postnatal development of the human cerebral cortex, vol 1-8. Harvard University Press, Cambridge, 1939-1967). Our method calculates normalized change vectors from the raw histological data, and then employs k-means cluster analysis of the change vectors to explore the population dynamics of neurons from 37 neocortical areas across eight postnatal developmental stages from birth to 72 months in 54 subjects. We show that the cortical "address" (Brodmann area/sub-area and layer) provides the necessary resolution to segregate neuron population changes into seven correlated "k-clusters" in k-means cluster analysis. The members in each k-cluster share a single change interval where the relative share of the cortex by the members undergoes its maximum change. The maximum change occurs in a different change interval for each k-cluster. Each k-cluster has at least one totally connected maximal "clique" which appears to correspond to cortical function. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11571-010-9103-3) contains supplementary material, which is available to authorized users.

Entities:  

Keywords:  Broca’s area; Network clique; Primary visual cortex; Retrosplenial cortex; Sensorimotor

Year:  2010        PMID: 21629587      PMCID: PMC2866365          DOI: 10.1007/s11571-010-9103-3

Source DB:  PubMed          Journal:  Cogn Neurodyn        ISSN: 1871-4080            Impact factor:   5.082


  37 in total

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