Literature DB >> 7119173

Anatomical binding of intrinsic connections in striate cortex of tree shrews (Tupaia glis).

K S Rockland, J S Lund, A L Humphrey.   

Abstract

The intrinsic connectivity of striate cortex was investigated by injecting horseradish peroxidase (HRP) into this area in tree shrews. Such HRP injections demonstrated periodically organized, stripelike connections within area 17. These stripes occur in layers I-IIIA and consist of a small number or retrogradely filled neurons, some clearly pyramidal, together with HRP-labeled axon terminals. HRP-filled axons trunks run between labeled stripes, interconnecting adjacent and distant regions of the stripe pattern. Correlation with Golgi-stained tissue suggests that these stripes are horizontally interconnected by pyramidal neurons with long intracortical axon collaterals (followed for distances over 1 mm from the soma). The HRP-labeled strips measure about 230 micrometers in width, with a center-to-center repeat distance of 450--500 micrometers. They have been mapped over an 8 mm2 area of striate cortex and would thus seem capable of effecting lateral interactions over considerable portions of the retinotopic map. In their dimensions and overall pattern, these anatomical stripes resemble the 2-deoxyglucose (2-DG) bands resulting from visual stimulation of trees shrews with stripes of a single orientation. While the functional role of the HRP-labeled stripes is unclear, their similarities with the 2-DG pattern raise the intriguing possibility that they may be related to orientation selectivity. The striking regularity of these extensive lateral interconnections emphasizes the importance of horizontal intralaminar connections within the cortex.

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Year:  1982        PMID: 7119173     DOI: 10.1002/cne.902090105

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


  41 in total

1.  How does connectivity between cortical areas depend on brain size? Implications for efficient computation.

Authors:  Jan Karbowski
Journal:  J Comput Neurosci       Date:  2003 Nov-Dec       Impact factor: 1.621

2.  Optogenetic spatial and temporal control of cortical circuits on a columnar scale.

Authors:  Arani Roy; Jason J Osik; Neil J Ritter; Shen Wang; James T Shaw; József Fiser; Stephen D Van Hooser
Journal:  J Neurophysiol       Date:  2015-12-02       Impact factor: 2.714

3.  Areal specialization of pyramidal cell structure in the visual cortex of the tree shrew: a new twist revealed in the evolution of cortical circuitry.

Authors:  Guy N Elston; Alejandra Elston; Vivien Casagrande; Jon H Kaas
Journal:  Exp Brain Res       Date:  2005-01-20       Impact factor: 1.972

4.  Spatial distribution of inhibitory synaptic connections during development of ferret primary visual cortex.

Authors:  Bingzhong Chen; Kaoutar Boukamel; Joseph P-Y Kao; Birgit Roerig
Journal:  Exp Brain Res       Date:  2004-10-19       Impact factor: 1.972

5.  Stereotypical bouton clustering of individual neurons in cat primary visual cortex.

Authors:  Tom Binzegger; Rodney J Douglas; Kevan A C Martin
Journal:  J Neurosci       Date:  2007-11-07       Impact factor: 6.167

6.  Learning to link visual contours.

Authors:  Wu Li; Valentin Piëch; Charles D Gilbert
Journal:  Neuron       Date:  2008-02-07       Impact factor: 17.173

7.  Spatially distributed responses induced by contrast reversal in cat visual cortex.

Authors:  M Kitano; T Kasamatsu; A M Norcia; E E Sutter
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

8.  Dual action of a ligand for Eph receptor tyrosine kinases on specific populations of axons during the development of cortical circuits.

Authors:  V Castellani; Y Yue; P P Gao; R Zhou; J Bolz
Journal:  J Neurosci       Date:  1998-06-15       Impact factor: 6.167

9.  Membrane-associated molecules regulate the formation of layer-specific cortical circuits.

Authors:  V Castellani; J Bolz
Journal:  Proc Natl Acad Sci U S A       Date:  1997-06-24       Impact factor: 11.205

10.  A comparison of visual callosal organization in normal, bilaterally enucleated and congenitally anophthalmic mice.

Authors:  R W Rhoades; R D Mooney; S E Fish
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

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