Literature DB >> 3584547

Retinopretectal and accessory optic projections of normal mice and the OKN-defective mutant mice beige, beige-J, and pearl.

M W Pak, R A Giolli, L H Pinto, N J Mangini, K M Gregory, J W Vanable.   

Abstract

Retinal projections to the pretectal and terminal accessory optic nuclei were studied in normal wild-type mice and mutant mice with abnormal optokinetic nystagmus (OKN, Mangini, Vanable, Williams, and Pinto: J. Comp. Neurol. 241:191-209, '85). The mutants used were pearl, which exhibits an inverted OKN in response to stimulation of only the temporal retina, and beige and beige-J, which show inverted OKN in response to stimulation of only the temporal retina and, in addition, exhibit eye movements with a vertical component in response to horizontally moving, full-field stimuli. These projections were studied following intraocular injections of 3H-proline or horseradish peroxidase (HRP) with, respectively, light microscopic autoradiography or HRP histochemistry. In wild-type mice, strong contralateral retinal projections covered the entire nucleus of the optic tract, the anterior and posterior divisions of the olivary pretectal nucleus, and the posterior pretectal nucleus. Similar heavy contralateral projections were distributed over the dorsal and medial terminal nuclei of the accessory optic system. Also, terminals sparsely covered the entire neuropil of the contralateral lateral terminal nucleus in some but not all wild-type mice. The most prominent accessory optic input was to the medial terminal nucleus and was provided by the inferior fasciculus of the accessory optic tract. A typical mammalian superior fasciculus of the accessory optic system with anterior, middle, and posterior components was present. Ipsilateral label was found in anterior and posterior olivary pretectal nuclei in all of the wild-type animals, but was found inconsistently in the ipsilateral terminal accessory optic nuclei. The pattern of contralateral retinal projection to the nucleus of the optic tract and posterior pretectal nucleus in mutants was indistinguishable from that seen in the normal wild-type mice. However, retinal inputs to the ipsilateral anterior and posterior olivary pretectal nuclei were significantly reduced in pearl mutants and were exceedingly sparse in the beige and beige-J mutant mice, while the contralateral inputs to these nuclei were increased in a complementary fashion in the mutants. The labeling of the accessory optic input to the contralateral dorsal terminal nucleus appeared to be substantially reduced in all of the mutant mice. The size of the principal accessory optic fascicle, the inferior fasciculus, was significantly smaller in beige, beige-J, and pearl mice; this reduction was greater in the beige and beige-J than in the pearl mice.(ABSTRACT TRUNCATED AT 400 WORDS)

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Mesh:

Year:  1987        PMID: 3584547     DOI: 10.1002/cne.902580311

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


  14 in total

1.  The pearl mutation accelerates the schedule of natural cell death in the early postnatal retina.

Authors:  M A Williams; L G Piñon; R Linden; L H Pinto
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

2.  Central projections of melanopsin-expressing retinal ganglion cells in the mouse.

Authors:  Samer Hattar; Monica Kumar; Alexander Park; Patrick Tong; Jonathan Tung; King-Wai Yau; David M Berson
Journal:  J Comp Neurol       Date:  2006-07-20       Impact factor: 3.215

3.  Dynamic expression of transcription factor Brn3b during mouse cranial nerve development.

Authors:  Szilard Sajgo; Seid Ali; Octavian Popescu; Tudor Constantin Badea
Journal:  J Comp Neurol       Date:  2015-09-29       Impact factor: 3.215

4.  Contactin-4 mediates axon-target specificity and functional development of the accessory optic system.

Authors:  Jessica A Osterhout; Benjamin K Stafford; Phong L Nguyen; Yoshihiro Yoshihara; Andrew D Huberman
Journal:  Neuron       Date:  2015-05-07       Impact factor: 17.173

5.  Genetic dissection of retinal inputs to brainstem nuclei controlling image stabilization.

Authors:  Onkar S Dhande; Maureen E Estevez; Lauren E Quattrochi; Rana N El-Danaf; Phong L Nguyen; David M Berson; Andrew D Huberman
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

6.  Reduced light sensitivity of the circadian clock in a hypopigmented mouse mutant.

Authors:  M H Vitaterna; J C Wu; F W Turek; L H Pinto
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

Review 7.  Retinal ganglion cell maps in the brain: implications for visual processing.

Authors:  Onkar S Dhande; Andrew D Huberman
Journal:  Curr Opin Neurobiol       Date:  2013-11-19       Impact factor: 6.627

8.  Elevated dark-adapted thresholds in hypopigmented mice measured with a water maze screening apparatus.

Authors:  J M Hayes; G W Balkema
Journal:  Behav Genet       Date:  1993-07       Impact factor: 2.805

9.  A Cre-dependent, anterograde transsynaptic viral tracer for mapping output pathways of genetically marked neurons.

Authors:  Liching Lo; David J Anderson
Journal:  Neuron       Date:  2011-12-22       Impact factor: 17.173

10.  Functional assembly of accessory optic system circuitry critical for compensatory eye movements.

Authors:  Lu O Sun; Colleen M Brady; Hugh Cahill; Timour Al-Khindi; Hiraki Sakuta; Onkar S Dhande; Masaharu Noda; Andrew D Huberman; Jeremy Nathans; Alex L Kolodkin
Journal:  Neuron       Date:  2015-05-07       Impact factor: 17.173

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