Evidence map›Paper›PMID 25649160›Full record

ArticleDevelopmental neurobiology2015

Ephrin-As are required for the topographic mapping but not laminar choice of physiologically distinct RGC types.

Neal T Sweeney, Kiely N James, Emily C Sales, David A Feldheim

Abstract read
In one paragraph

Article in Developmental neurobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Neal T SweeneyMolecular, Cell & Developmental Biology, University of California, Santa Cruz, Santa Cruz, California, 95064.
Kiely N JamesMolecular, Cell & Developmental Biology, University of California, Santa Cruz, Santa Cruz, California, 95064.
Emily C SalesMolecular, Cell & Developmental Biology, University of California, Santa Cruz, Santa Cruz, California, 95064.
David A FeldheimMolecular, Cell & Developmental Biology, University of California, Santa Cruz, Santa Cruz, California, 95064.

Funding

Development of Retinal Ganglion Cell typesR01EY022117 · NEI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI FELDHEIM, DAVID A · 2012 to 2020
$3.5M
TOPOGRAPHIC MAPPING LABELS IN VISUAL DEVELOPMENTR01EY014689 · NEI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI FELDHEIM, DAVID A · 2003 to 2012
$3.1M
NEI NIH HHS R01 EY014689NEI NIH HHS R01 EY022117NEI NIH HHS R01EY022117
6 · The paper itself

Abstract

In the retinocollicular projection, the axons from functionally distinct retinal ganglion cell (RGC) types form synapses in a stereotypical manner along the superficial to deep axis of the superior colliculus (SC). Each lamina contains an orderly topographic map of the visual scene but different laminae receive inputs from distinct sets of RGCs, and inputs to each lamina are aligned with the others to integrate parallel streams of visual information. To determine the relationship between laminar organization and topography of physiologically defined RGC types, we used genetic and anatomical axon tracing techniques in wild type and ephrin-A mutant mice. We find that adjacent RGCs of the same physiological type can send axons to both ectopic and normal topographic locations, supporting a penetrance model for ephrin-A independent mapping cues. While the overall laminar organization in the SC is unaffected in ephrin-A2/A5 double mutant mice, analysis of the laminar locations of ectopic terminations shows that the topographic maps of different RGC types are misaligned. These data lend support to the hypothesis that the retinocollicular projection is a superimposition of a number of individual two-dimensional topographic maps that originate from specific types of RGCs, require ephrin-A signaling, and form independently of the other maps.

Indexed as

Brain MappingVisual PathwaysAmino AcidsAnimalsBrainEphrinsMiceMice, TransgenicMutationRetinal Ganglion CellsSuperior ColliculiAmino AcidsdolaisoleucineEphrinsephrin-Atopographic mappingvisual system development

Identifiers

PMID25649160
PMCPMC4437846

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.