Literature DB >> 1586644

Nonlagged relay cells and interneurons in the cat lateral geniculate nucleus: receptive-field properties and retinal inputs.

D N Mastronarde1.   

Abstract

Simultaneous recording in the cat's retina and lateral geniculate nucleus (LGN) was used to find excitatory inputs to LGN cells. These recordings, correlated with measurements of LGN cell receptive-field properties, suggested new functional subdivisions of LGN cells. Distinctions between lagged and nonlagged cells were described before (Mastronarde, 1987a,b; Mastronarde et al., 1991), classification of nonlagged cells is examined here. The XS-type relay cells described before (Mastronarde, 1987a,b) each had detectable excitatory input from only one retinal X cell. Cells that received significant input from more than one retinal X cell were of three kinds: relay cells with pure X input (XM); relay cells with mixed X and Y input (X/Y); and cells that could not be antidromically activated from visual cortex (XI). In the series of relay cells, XS-XM-X/Y-Y, cells had progressively larger receptive-field centers, lower spatial resolution, and faster and more Y-like responses to various stimuli. XI cells resembled XM and X/Y cells in some respects but tended to have higher maintained firing rates, more sustained responses, and weaker surround suppression of the center response. The distinctness of XS, XM, X/Y, XI, and Y from each other was examined with a modification of discriminant analysis that allowed cells to lack measurements for some parameters. Any given pair of categories could be distinguished reliably with only three parameters, although less so for X/Y-Y. In particular, XI cells were distinguishable from relay cells by properties other than the results of cortical stimulation, thus supporting the identity of XI cells as a separate class of X interneurons. Two discontinuities in the behavior of retinal input suggest that XM cells are a separate class from XS and X/Y cells: (1) LGN X cells received either no detectable input from any of the retinal X cells adjacent to their main input, or an easily detectable amount from several such cells; and (2) cells received either no Y input or a certain minimum amount. No such discontinuity in input underlies the distinction between X/Y and Y cells. LGN Y cells were also heterogeneous. Those with substantial input from more than one retinal Y cell had larger receptive fields and a greater preference for fast-moving stimuli than did Y cells dominated by a single input. Three Y cells could not be antidromically activated. They tended to differ from Y relay cells and resemble X interneurons in several ways.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1992        PMID: 1586644     DOI: 10.1017/s0952523800004934

Source DB:  PubMed          Journal:  Vis Neurosci        ISSN: 0952-5238            Impact factor:   3.241


  32 in total

1.  Development of response timing and direction selectivity in cat visual thalamus and cortex.

Authors:  Alan B Saul; Jordan C Feidler
Journal:  J Neurosci       Date:  2002-04-01       Impact factor: 6.167

2.  Rules of connectivity between geniculate cells and simple cells in cat primary visual cortex.

Authors:  J M Alonso; W M Usrey; R C Reid
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  Brainstem modulation of visual response properties of single cells in the dorsal lateral geniculate nucleus of cat.

Authors:  I T Fjeld; O Ruksenas; P Heggelund
Journal:  J Physiol       Date:  2002-09-01       Impact factor: 5.182

Review 4.  Retinogeniculate connections: A balancing act between connection specificity and receptive field diversity.

Authors:  J-M Alonso; C-I Yeh; C Weng; C Stoelzel
Journal:  Prog Brain Res       Date:  2006       Impact factor: 2.453

Review 5.  Inhibitory circuits for visual processing in thalamus.

Authors:  Xin Wang; Friedrich T Sommer; Judith A Hirsch
Journal:  Curr Opin Neurobiol       Date:  2011-07-13       Impact factor: 6.627

6.  Interspike interval analysis of retinal ganglion cell receptive fields.

Authors:  Daniel L Rathbun; Henry J Alitto; Theodore G Weyand; W Martin Usrey
Journal:  J Neurophysiol       Date:  2007-05-23       Impact factor: 2.714

7.  Functional consequences of neuronal divergence within the retinogeniculate pathway.

Authors:  Chun-I Yeh; Carl R Stoelzel; Chong Weng; Jose-Manuel Alonso
Journal:  J Neurophysiol       Date:  2009-01-28       Impact factor: 2.714

8.  Visual stimuli modulate precise synchronous firing within the thalamus.

Authors:  Jose-Manuel Alonso; Chun-I Yeh; Carl R Stoelzel
Journal:  Thalamus Relat Syst       Date:  2008

9.  Visual orientation and directional selectivity through thalamic synchrony.

Authors:  Garrett B Stanley; Jianzhong Jin; Yushi Wang; Gaëlle Desbordes; Qi Wang; Michael J Black; Jose-Manuel Alonso
Journal:  J Neurosci       Date:  2012-06-27       Impact factor: 6.167

10.  Statistical wiring of thalamic receptive fields optimizes spatial sampling of the retinal image.

Authors:  Luis M Martinez; Manuel Molano-Mazón; Xin Wang; Friedrich T Sommer; Judith A Hirsch
Journal:  Neuron       Date:  2014-02-19       Impact factor: 17.173

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