Evidence map›Paper›PMID 25873107›Full record

ArticleVisual neuroscience2015

CaV3.2 KO mice have altered retinal waves but normal direction selectivity.

Aaron M Hamby, Juliana M Rosa, Ching-Hsiu Hsu, Marla B Feller

Abstract read
In one paragraph

Article in Visual neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. The Role of Calcium Signaling in Sensorineural Hearing Loss.International journal of medical sciences · 2025
    Review
  2. Regulation of Presynaptic Calcium Channels.Advances in neurobiology · 2023
    Article
  3. Review
  4. Breeding of CaScientific reports · 2021
    Article
  5. Article
  6. Activity-dependent development of visual receptive fields.Current opinion in neurobiology · 2017
    Review
  7. Article
  8. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Aaron M HambyDepartment of Molecular and Cell Biology,University of California,Berkeley,Berkeley,California.
Juliana M RosaDepartment of Molecular and Cell Biology,University of California,Berkeley,Berkeley,California.
Ching-Hsiu HsuDepartment of Molecular and Cell Biology,University of California,Berkeley,Berkeley,California.
Marla B FellerDepartment of Molecular and Cell Biology,University of California,Berkeley,Berkeley,California.

Funding

UC Berkeley Vision Science COREP30EY003176 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RICHARD H KRAMER · 1985 to 2026
$16.4M
The Function of Neural Activity in Developing RetinaR01EY013528 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Marla Feller · 2002 to 2026
$8.1M
Development of direction selectivity in the retinaR01EY019498 · NEI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Marla Feller · 2009 to 2026
$6.6M
The Role of Spontaneous Neural Activity in the Development of Direction SelectiviF31NS071784 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HAMBY, AARON MICHAEL · 2011 to 2012
$52k
NEI NIH HHS P30 EY003176NEI NIH HHS P30EY003176NEI NIH HHS R01 EY013528NEI NIH HHS R01EY013528NEI NIH HHS R01 EY019498NEI NIH HHS R01EY019498NINDS NIH HHS 5F31NS071784NINDS NIH HHS F31 NS071784
6 · The paper itself

Abstract

Early in development, before the onset of vision, the retina establishes direction-selective responses. During this time period, the retina spontaneously generates bursts of action potentials that propagate across its extent. The precise spatial and temporal properties of these "retinal waves" have been implicated in the formation of retinal projections to the brain. However, their role in the development of direction selective circuits within the retina has not yet been determined. We addressed this issue by combining multielectrode array and cell-attached recordings to examine mice that lack the CaV3.2 subunit of T-type Ca2+ channels (CaV3.2 KO) because these mice exhibit disrupted waves during the period that direction selective circuits are established. We found that the spontaneous activity of these mice displays wave-associated bursts of action potentials that are altered from that of control mice: the frequency of these bursts is significantly decreased and the firing rate within each burst is reduced. Moreover, the projection patterns of the retina demonstrate decreased eye-specific segregation in the dorsal lateral geniculate nucleus (dLGN). However, after eye-opening, the direction selective responses of CaV3.2 KO direction selective ganglion cells (DSGCs) are indistinguishable from those of wild-type DSGCs. Our data indicate that although the temporal properties of the action potential bursts associated with retinal waves are important for activity-dependent refining of retinal projections to central targets, they are not critical for establishing direction selectivity in the retina.

Indexed as

Vision DisordersAction PotentialsAnimalsAnimals, NewbornCalcium Channels, T-TypeGeniculate BodiesIn Vitro TechniquesMiceMice, Inbred C57BLMice, KnockoutOrientationRetinaRetinal Ganglion CellsVisual PathwaysCacna1h protein, mouseCalcium Channels, T-TypeNeurodevelopment

Identifiers

PMID25873107
PMCPMC4547621

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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.