Literature DB >> 11353027

Visual response properties of neurons in the LGN of normally reared and visually deprived macaque monkeys.

J B Levitt1, R A Schumer, S M Sherman, P D Spear, J A Movshon.   

Abstract

It is now well appreciated that parallel retino-geniculo-cortical pathways exist in the monkey as in the cat, the species in which parallel visual pathways were first and most thoroughly documented. What remains unclear is precisely how many separate pathways pass through the parvo- and magnocellular divisions of the macaque lateral geniculate nucleus (LGN), what relationships-homologous or otherwise-these pathways have to the cat's X, Y, and W pathways, and whether these are affected by visual deprivation. To address these issues of classification and trans-species comparison, we used achromatic stimuli to obtain an extensive set of quantitative measurements of receptive field properties in the parvo- and magnocellular laminae of the LGN of nine macaque monkeys: four normally reared and five monocularly deprived of vision by lid suture near the time of birth. In agreement with previous studies, we find that on average magnocellular neurons differ from parvocellular neurons by having shorter response latencies to optic chiasm stimulation, greater sensitivity to luminance contrast, and better temporal resolution. Magnocellular laminae are also distinguished by containing neurons that summate luminance over their receptive fields nonlinearly (Y cells) and whose temporal response phases decrease with increasing stimulus contrast (indicative of a contrast gain control mechanism). We found little evidence for major differences between magno- and parvocellular neurons on the basis of most spatial parameters except that at any eccentricity, the neurons with the smallest receptive field centers tended to be parvocellular. All parameters were distributed unimodally and continuously through the parvo- and magnocellular populations, giving no indications of subpopulations within each division. Monocular deprivation led to clear anatomical effects: cells in deprived-eye laminae were pale and shrunken compared with those in nondeprived eye laminae, and Cat-301 immunoreactivity in deprived laminae was essentially uniformly abolished. However, deprivation had only subtle effects on the response properties of LGN neurons. Neurons driven by the deprived eye in both magno- and parvocellular laminae had lower nonlinearity indices (i.e., summed signals across their receptive fields more linearly) and were somewhat less responsive. In magnocellular laminae driven by the deprived eye, neuronal response latencies to stimulation of the optic chiasm were slightly shorter than those in the nondeprived laminae, and receptive field surrounds were a bit stronger. No other response parameters were affected by deprivation, and there was no evidence for loss of a specific cell class as in the cat.

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Year:  2001        PMID: 11353027     DOI: 10.1152/jn.2001.85.5.2111

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  51 in total

1.  The timing of response onset and offset in macaque visual neurons.

Authors:  Wyeth Bair; James R Cavanaugh; Matthew A Smith; J Anthony Movshon
Journal:  J Neurosci       Date:  2002-04-15       Impact factor: 6.167

2.  Different circuits for ON and OFF retinal ganglion cells cause different contrast sensitivities.

Authors:  Kareem A Zaghloul; Kwabena Boahen; Jonathan B Demb
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

3.  Seeing blur: 'motion sharpening' without motion.

Authors:  Mark A Georgeson; Stephen T Hammett
Journal:  Proc Biol Sci       Date:  2002-07-22       Impact factor: 5.349

Review 4.  Corticogeniculate feedback and visual processing in the primate.

Authors:  Farran Briggs; W Martin Usrey
Journal:  J Physiol       Date:  2010-08-19       Impact factor: 5.182

5.  A comparison of visual responses in the lateral geniculate nucleus of alert and anaesthetized macaque monkeys.

Authors:  Henry J Alitto; Bartlett D Moore; Daniel L Rathbun; W Martin Usrey
Journal:  J Physiol       Date:  2010-07-05       Impact factor: 5.182

6.  Properties of pattern and component direction-selective cells in area MT of the macaque.

Authors:  Helena X Wang; J Anthony Movshon
Journal:  J Neurophysiol       Date:  2015-11-11       Impact factor: 2.714

7.  Long-term Monocular Deprivation during Juvenile Critical Period Disrupts Binocular Integration in Mouse Visual Thalamus.

Authors:  Carey Y L Huh; Karim Abdelaal; Kirstie J Salinas; Diyue Gu; Jack Zeitoun; Dario X Figueroa Velez; John P Peach; Charless C Fowlkes; Sunil P Gandhi
Journal:  J Neurosci       Date:  2019-11-25       Impact factor: 6.167

8.  Human vision with a lesion of the parvocellular pathway: an optic neuritis model for selective contrast sensitivity deficits with severe loss of midget ganglion cell function.

Authors:  Amal M Al-Hashmi; Daniel J Kramer; Kathy T Mullen
Journal:  Exp Brain Res       Date:  2011-10-18       Impact factor: 1.972

9.  Modeling lateral geniculate nucleus response with contrast gain control. Part 1: formulation.

Authors:  Davis Cope; Barbara Blakeslee; Mark E McCourt
Journal:  J Opt Soc Am A Opt Image Sci Vis       Date:  2013-11-01       Impact factor: 2.129

10.  Functional maturation of the macaque's lateral geniculate nucleus.

Authors:  J Anthony Movshon; Lynne Kiorpes; Michael J Hawken; James R Cavanaugh
Journal:  J Neurosci       Date:  2005-03-09       Impact factor: 6.167

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