Literature DB >> 7298914

Areal and laminar distribution of neurons interconnecting the central visual cortical areas 17, 18, 19, and MT in squirrel monkey (Saimiri).

J Tigges, M Tigges, S Anschel, N A Cross, W D Letbetter, R L McBride.   

Abstract

The retrogradely transported horseradish peroxidase (HRP) method was used to study the areal and laminar distribution of neurons sending their axons to ipsilateral and contralateral visual cortical areas 17, 18, 19, and MT in the squirrel monkey. Further details regarding neuron type (stellate or pyramidal), size class, and spatial grouping of the cells making these corticocortical connections also were obtained. All interareal connections are reciprocal. Ipsilaterally, such connections exist between areas 17 and 18, 17 and MT, 18 and 19, 18 and MT, and 19 and MT. In addition, areas 18, 19, and MT receive association fibers from the ipsilateral frontal eye field; when combined with previous findings, these results indicate the existence of reciprocal connections between area 18 and the frontal eye field and between area MT and the frontal eye field. Each of areas 18, 19, and MT. Area 17 has only weak callosal connections. Both the ipsilateral and the contralateral connections are topographically organized such that they obey a hodological principle of visuotopic connectivity: that is, only representations of the same part of the visual field are interconnected. With regard to layers of origin, the callosal neurons of these visual areas conform to the general concept of corticocortical fibers arising from supragranular layers in that most of them are located in layer IIIb; only a few of them reside at the junction between layers V and VI. On the other hand, for all the visuocortical connections investigated, the anteriormost area of a reciprocally interconnected pair has its association neurons located predominantly in the infragranular layers while the posteriormost area has its association neurons located primarily in layer III. All callosal fibers and most association fibers arise from pyramidal cells. The callosal cells are larger and reside at a deeper level in layer III than neurons with ipsilateral corticocortical connections. However, some of the association cells at the junction of layers V and VI in area 17 which project to area MT are relatively large and may include the solitary cells of Meynert; but medium-sized pyramidal cells also participate in this projection. In area 17, some association neurons in layers IIIb and IIIc which project to area 18, as well as some in layer IIIc which project to area MT, are most likely stellate cells. Several different patterns of cell groupings were observed for the central representation interconnections. Neither ipsilateral area MT nor any of the contralateral visuocortical areas had multiple groupings of labeled neurons. The ipsilateral projections from area 17 to 18, 17 to MT, and 18 to 19 were arranged similarly according to a plan involving separate, multiple loci of origin for cells projecting to a small and isolated subregion of the central representation in the target cortical area; following larger injections, cells throughout the central representation of the projecting cortex were labeled...

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Year:  1981        PMID: 7298914     DOI: 10.1002/cne.902020407

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


  26 in total

1.  Laminar distribution of neurons in extrastriate areas projecting to visual areas V1 and V4 correlates with the hierarchical rank and indicates the operation of a distance rule.

Authors:  P Barone; A Batardiere; K Knoblauch; H Kennedy
Journal:  J Neurosci       Date:  2000-05-01       Impact factor: 6.167

2.  Expression of GAP-43 and SCG10 mRNAs in lateral geniculate nucleus of normal and monocularly deprived macaque monkeys.

Authors:  N Higo; T Oishi; A Yamashita; K Matsuda; M Hayashi
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

3.  Responses of neurons in the middle temporal visual area after long-standing lesions of the primary visual cortex in adult new world monkeys.

Authors:  Christine E Collins; David C Lyon; Jon H Kaas
Journal:  J Neurosci       Date:  2003-03-15       Impact factor: 6.167

4.  Optical imaging of visually evoked responses in prosimian primates reveals conserved features of the middle temporal visual area.

Authors:  Xiangmin Xu; Christine E Collins; Peter M Kaskan; Ilya Khaytin; Jon H Kaas; Vivien A Casagrande
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-24       Impact factor: 11.205

5.  Regular structural organization of intrahemisphere interzonal connections in the visual cortex of the cat.

Authors:  F N Makarov; V A Lyakhovetskii; L A Markova
Journal:  Neurosci Behav Physiol       Date:  2004-11

Review 6.  The importance of being agranular: a comparative account of visual and motor cortex.

Authors:  Stewart Shipp
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2005-04-29       Impact factor: 6.237

7.  Occipital network for figure/ground organization.

Authors:  Lora T Likova; Christopher W Tyler
Journal:  Exp Brain Res       Date:  2008-07-05       Impact factor: 1.972

8.  Patterns of projections from area 2 of the sensory cortex to area 3a and to the motor cortex in cats.

Authors:  L L Porter
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

9.  Anatomical evidence for classical and extra-classical receptive field completion across the discontinuous horizontal meridian representation of primate area V2.

Authors:  Janelle Jeffs; Jennifer M Ichida; Frederick Federer; Alessandra Angelucci
Journal:  Cereb Cortex       Date:  2008-08-28       Impact factor: 5.357

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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