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Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations

Cortical GABAergic (γ-aminobutyric acidergic) neurons include a recently identified subset whose projections extend over relatively long distances in adult rodents and primates. A number of these inhibitory projection neurons are located in and above the conventionally identified white matter, sugge...

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Autores principales: Clancy, Barbara, Teague-Ross, Terri J., Nagarajan, Radhakrishnan
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779099/
https://www.ncbi.nlm.nih.gov/pubmed/19936319
http://dx.doi.org/10.3389/neuro.05.020.2009
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author Clancy, Barbara
Teague-Ross, Terri J.
Nagarajan, Radhakrishnan
author_facet Clancy, Barbara
Teague-Ross, Terri J.
Nagarajan, Radhakrishnan
author_sort Clancy, Barbara
collection PubMed
description Cortical GABAergic (γ-aminobutyric acidergic) neurons include a recently identified subset whose projections extend over relatively long distances in adult rodents and primates. A number of these inhibitory projection neurons are located in and above the conventionally identified white matter, suggesting their persistence from, or a correspondence with, the developmental subplate. GABAergic and subplate neurons share some unique properties unlike those of the more prevalent pyramidal neurons. To better understand the GABAergic and subplate populations, we constructed a database of neural developmental events common to the three species most frequently used in experimental studies: rat, mouse, and macaque, using data from the online database www.translatingtime.net as well as GABAergic and subplate developmental data from the empirical literature. We used a general linear model to test for similarities and differences, a valid approach because the sequence of most neurodevelopmental events is remarkably conserved across mammalian species. Similarities between the two rodent populations are striking, permitting us to identify developmental dates for GABAergic and subplate neural events in rats that were previously identified only in mice, as well as the timing in mouse development for events previously identified in rats. Primate comparative data are also compelling, although slight variability in statistical error measurement indicates differences in primate GABAergic and subplate events when compared to rodents. Although human extrapolations are challenging because fewer empirical data points are available, and because human data display more variability, we also produce estimates of dates for GABAergic and subplate neural events that have not yet been, or cannot be, determined empirically in humans.
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spelling pubmed-27790992009-11-20 Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations Clancy, Barbara Teague-Ross, Terri J. Nagarajan, Radhakrishnan Front Neuroanat Neuroscience Cortical GABAergic (γ-aminobutyric acidergic) neurons include a recently identified subset whose projections extend over relatively long distances in adult rodents and primates. A number of these inhibitory projection neurons are located in and above the conventionally identified white matter, suggesting their persistence from, or a correspondence with, the developmental subplate. GABAergic and subplate neurons share some unique properties unlike those of the more prevalent pyramidal neurons. To better understand the GABAergic and subplate populations, we constructed a database of neural developmental events common to the three species most frequently used in experimental studies: rat, mouse, and macaque, using data from the online database www.translatingtime.net as well as GABAergic and subplate developmental data from the empirical literature. We used a general linear model to test for similarities and differences, a valid approach because the sequence of most neurodevelopmental events is remarkably conserved across mammalian species. Similarities between the two rodent populations are striking, permitting us to identify developmental dates for GABAergic and subplate neural events in rats that were previously identified only in mice, as well as the timing in mouse development for events previously identified in rats. Primate comparative data are also compelling, although slight variability in statistical error measurement indicates differences in primate GABAergic and subplate events when compared to rodents. Although human extrapolations are challenging because fewer empirical data points are available, and because human data display more variability, we also produce estimates of dates for GABAergic and subplate neural events that have not yet been, or cannot be, determined empirically in humans. Frontiers Research Foundation 2009-10-06 /pmc/articles/PMC2779099/ /pubmed/19936319 http://dx.doi.org/10.3389/neuro.05.020.2009 Text en Copyright © 2009 Clancy, Teague-Ross and Nagarajan. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Clancy, Barbara
Teague-Ross, Terri J.
Nagarajan, Radhakrishnan
Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title_full Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title_fullStr Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title_full_unstemmed Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title_short Cross-Species Analyses of the Cortical GABAergic and Subplate Neural Populations
title_sort cross-species analyses of the cortical gabaergic and subplate neural populations
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2779099/
https://www.ncbi.nlm.nih.gov/pubmed/19936319
http://dx.doi.org/10.3389/neuro.05.020.2009
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