Literature DB >> 10223310

Cellular distribution of the calcium-binding proteins parvalbumin, calbindin, and calretinin in the neocortex of mammals: phylogenetic and developmental patterns.

P R Hof1, I I Glezer, F Condé, R A Flagg, M B Rubin, E A Nimchinsky, D M Vogt Weisenhorn.   

Abstract

The three calcium-binding proteins parvalbumin, calbindin, and calretinin are found in morphologically distinct classes of inhibitory interneurons as well as in some pyramidal neurons in the mammalian neocortex. Although there is a wide variability in the qualitative and quantitative characteristics of the neocortical subpopulations of calcium-binding protein-immunoreactive neurons in mammals, most of the available data show that there is a fundamental similarity among the mammalian species investigated so far, in terms of the distribution of parvalbumin, calbindin, and calretinin across the depth of the neocortex. Thus, calbindin- and calretinin-immunoreactive neurons are predominant in layers II and III, but are present across all cortical layers, whereas parvalbumin-immunoreactive neurons are more prevalent in the middle and lower cortical layers. These different neuronal populations have well defined regional and laminar distribution, neurochemical characteristics and synaptic connections, and each of these cell types displays a particular developmental sequence. Most of the available data on the development, distribution and morphological characteristics of these calcium-binding proteins are from studies in common laboratory animals such as the rat, mouse, cat, macaque monkey, as well as from postmortem analyses in humans, but there are virtually no data on other species aside of a few incidental reports. In the context of the evolution of mammalian neocortex, the distribution and morphological characteristics of calcium-binding protein-immunoreactive neurons may help defining taxon-specific patterns that may be used as reliable phylogenetic traits. It would be interesting to extend such neurochemical analyses of neuronal subpopulations to other species to assess the degree to which neurochemical specialization of particular neuronal subtypes, as well as their regional and laminar distribution in the cerebral cortex, may represent sets of derived features in any given mammalian order. This could be particularly interesting in view of the consistent differences in neurochemical typology observed in considerably divergent orders such as cetaceans and certain families of insectivores and metatherians, as well as in monotremes. The present article provides an overview of calcium-binding protein distribution across a large number of representative mammalian species and a review of their developmental patterns in the species where data are available. This analysis demonstrates that while it is likely that the developmental patterns are quite consistent across species, at least based on the limited number of species for which ontogenetic data exist, the distribution and morphology of calcium-binding protein-containingneurons varies substantially among mammalian orders and that certain species show highly divergent patterns compared to closely related taxa. Interestingly, primates, carnivores, rodents and tree shrews appear closely related on the basis of the observed patterns, marsupials show some affinities with that group, whereas prototherians have unique patterns. Our findings also support the relationships of cetaceans and ungulates, and demonstrates possible affinities between carnivores and ungulates, as well as the existence of common, probably primitive, traits in cetaceans and insectivores.

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Year:  1999        PMID: 10223310     DOI: 10.1016/s0891-0618(98)00065-9

Source DB:  PubMed          Journal:  J Chem Neuroanat        ISSN: 0891-0618            Impact factor:   3.052


  108 in total

1.  A neuronal morphologic type unique to humans and great apes.

Authors:  E A Nimchinsky; E Gilissen; J M Allman; D P Perl; J M Erwin; P R Hof
Journal:  Proc Natl Acad Sci U S A       Date:  1999-04-27       Impact factor: 11.205

2.  Late development of the GABAergic system in the human cerebral cortex and white matter.

Authors:  Gang Xu; Kevin G Broadbelt; Robin L Haynes; Rebecca D Folkerth; Natalia S Borenstein; Richard A Belliveau; Felicia L Trachtenberg; Joseph J Volpe; Hannah C Kinney
Journal:  J Neuropathol Exp Neurol       Date:  2011-10       Impact factor: 3.685

3.  Expression of the transcription factor, tailless, is required for formation of superficial cortical layers.

Authors:  P W Land; A P Monaghan
Journal:  Cereb Cortex       Date:  2003-09       Impact factor: 5.357

4.  Cortical white matter: beyond the pale remarks, main conclusions and discussion.

Authors:  Javier Defelipe; R Douglas Fields; Patrick R Hof; Malin Höistad; Ivica Kostovic; Gundela Meyer; Kathleen S Rockland
Journal:  Front Neuroanat       Date:  2010-03-24       Impact factor: 3.856

Review 5.  New insights into the classification and nomenclature of cortical GABAergic interneurons.

Authors:  Javier DeFelipe; Pedro L López-Cruz; Ruth Benavides-Piccione; Concha Bielza; Pedro Larrañaga; Stewart Anderson; Andreas Burkhalter; Bruno Cauli; Alfonso Fairén; Dirk Feldmeyer; Gord Fishell; David Fitzpatrick; Tamás F Freund; Guillermo González-Burgos; Shaul Hestrin; Sean Hill; Patrick R Hof; Josh Huang; Edward G Jones; Yasuo Kawaguchi; Zoltán Kisvárday; Yoshiyuki Kubota; David A Lewis; Oscar Marín; Henry Markram; Chris J McBain; Hanno S Meyer; Hannah Monyer; Sacha B Nelson; Kathleen Rockland; Jean Rossier; John L R Rubenstein; Bernardo Rudy; Massimo Scanziani; Gordon M Shepherd; Chet C Sherwood; Jochen F Staiger; Gábor Tamás; Alex Thomson; Yun Wang; Rafael Yuste; Giorgio A Ascoli
Journal:  Nat Rev Neurosci       Date:  2013-02-06       Impact factor: 34.870

6.  Crk and Crk-like play essential overlapping roles downstream of disabled-1 in the Reelin pathway.

Authors:  Tae-Ju Park; Tom Curran
Journal:  J Neurosci       Date:  2008-12-10       Impact factor: 6.167

7.  Parvalbumin and calbindin expression in parallel thalamocortical pathways in a gleaning bat, Antrozous pallidus.

Authors:  Heather Martin del Campo; Kevin Measor; Khaleel A Razak
Journal:  J Comp Neurol       Date:  2014-07-01       Impact factor: 3.215

8.  Thalamic connections of architectonic subdivisions of temporal cortex in grey squirrels (Sciurus carolinensis).

Authors:  Peiyan Wong; Omar A Gharbawie; Lynn E Luethke; Jon H Kaas
Journal:  J Comp Neurol       Date:  2008-10-01       Impact factor: 3.215

9.  Plasticity between neuronal pairs in layer 4 of visual cortex varies with synapse state.

Authors:  Ignacio Sáez; Michael J Friedlander
Journal:  J Neurosci       Date:  2009-12-02       Impact factor: 6.167

10.  Inhibitory interneurons of the human prefrontal cortex display conserved evolution of the phenotype and related genes.

Authors:  Chet C Sherwood; Mary Ann Raghanti; Cheryl D Stimpson; Muhammad A Spocter; Monica Uddin; Amy M Boddy; Derek E Wildman; Christopher J Bonar; Albert H Lewandowski; Kimberley A Phillips; Joseph M Erwin; Patrick R Hof
Journal:  Proc Biol Sci       Date:  2009-12-02       Impact factor: 5.349

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