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Research article summary (published 12 Oct 2009):

Direction-specific disruption of subcortical visual behavior and receptive fields in mice lacking the beta2 subunit of nicotinic acetylcholine receptor.

Full Abstract

Retinotopic mapping is a basic feature of visual system organization, but its role in processing visual information is unknown. Mutant mice lacking the beta2 subunit of nicotinic acetylcholine receptor have imprecise maps in both visual cortex (V1) and the superior colliculus (SC) due to the disruption of spontaneous retinal activity during development. Here, we use behavioral and physiological approaches to study their visual functions. We find that beta2-/- mice fail to track visual stimuli moving along the nasotemporal axis in a subcortical optomotor behavior, but track normally along the dorsoventral axis. In contrast, these mice display normal acuity along both axes in the visual water task, a behavioral test of cortical functions. Consistent with the behavioral results, we find that V1 neurons in beta2-/- mice have normal response properties, while SC neurons have disrupted receptive fields, including enlarged structure and decreased direction and orientation selectivity along the nasotemporal axis. The subcortical-specific deficits indicate that retinotopic map disruption has different impacts on the development of functional properties in V1 and the SC.

 

Author information

Author/s: Wang, Lupeng (L); Rangarajan, Krsna V (KV); Lawhn-Heath, Courtney A (CA); Sarnaik, Rashmi (R); Wang, Bor-Shuen (BS); Liu, Xiaorong (X); Cang, Jianhua (J);

Affiliation: Department of Neurobiology and Physiology and Interdepartmental Neuroscience Program, Northwestern University, Evanston, Illinois 60208, USA.

Grants: EY018621 (Agency:NEI NIH HHS) ; EY019034 (Agency:NEI NIH HHS)

Journal and publication information

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience (J Neurosci), published in United States. (Language: eng)

Reference: 2009-Oct; vol 29 (issue 41) : pp 12909-18

Dates: Created 2009/10/15; Completed 2009/10/30;

PMID: 19828805, status: MEDLINE (last retrieval date: 10/30/2009, IMS Date: )

Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.

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MeSH headings (categories)

This article was linked to the MESH Headings shown below.

Associated Chemicals: Chrnb2 protein, mouse (0) ; Receptors, Nicotinic (0)

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