Evidence map›Paper›PMID 18671302›Full record

ArticleThe Journal of comparative neurology2008

Probing neurochemical structure and function of retinal ON bipolar cells with a transgenic mouse.

Anuradha Dhingra, Pyroja Sulaiman, Ying Xu, Marie E Fina, Rüdiger W Veh, Noga Vardi

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
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

45 citing papers in PubMed, 65 citations in OpenAlex.

  1. Optogenetic vision restoration in the face of secondary and tertiary remodeling in the rd1 mouse retina.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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

6 authors at 2 institutions in 2 countries.

Anuradha DhingraDepartment of Neuroscience, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6058, USA.
Pyroja Sulaiman
Ying Xu
Marie E Fina
Rüdiger W Veh
Noga Vardi
University of Pennsylvania · USCharité - Universitätsmedizin Berlin · DE

Funding

Scientific TransparencyP30EY001583 · NEI · UNIVERSITY OF PENNSYLVANIA · PI CLAIRE H MITCHELL · 1985 to 2026
$19.5M
CHEMICAL ARCHITECTURE OF RETINAL CIRCUITSR01EY011105 · NEI · UNIVERSITY OF PENNSYLVANIA · PI VARDI, NOGA · 1995 to 2012
$6.2M
NEI NIH HHS EY11105NEI NIH HHS P30 EY001583NEI NIH HHS R01 EY011105
6 · The paper itself

Abstract

Retinal ON bipolar cells make up about 70% of all bipolar cells. Glutamate hyperpolarizes these cells by binding to the metabotropic glutamate receptor mGluR6, activating the G-protein G(o1), and closing an unidentified cation channel. To facilitate investigation of ON bipolar cells, we here report on the production of a transgenic mouse (Grm6-GFP) in which enhanced green fluorescent protein (EGFP), under control of mGluR6 promoter, was expressed in all and only ON bipolar cells. We used the mouse to determine density of ON bipolar cells, which in central retina was 29,600 cells/mm(2). We further sorted the fluorescent cells and created a pure ON bipolar cDNA library that was negative for photoreceptor unique genes. With this library, we determined expression of 27 genes of interest. We obtained positive transcripts for G(o) interactors: regulators of G-protein signaling (RGS), Ret-RGS1 (a variant of RGS20), RGS16, RGS7, purkinje cell protein 2 (PCP2, also called L7 or GPSM4), synembryn (RIC-8), LGN (GPSM2), RAP1GAP, and Gbeta5; cGMP modulators: guanylyl cyclase (GC) 1alpha1, GC1beta1, phosphodiesterase (PDE) 1C, and PDE9A; and channels: inwardly rectifying potassium channel Kir2.4, transient receptor potential TRPC2, and sperm-specific cation channels CatSper 2-4. The following transcripts were not found in our library: AGS3 (GPSM1), RGS10, RGS19 (GAIP), calbindin, GC1alpha2, GC1beta2, PDE5, PDE2A, amiloride-sensitive sodium channel ACCN4, and CatSper1. We then localized Kir2.4 to several cell types and showed that, in ON bipolar cells, the channel concentrates in their dendritic tips. The channels and modulators found in ON bipolar cells likely shape their light response. Additional uses of the Grm6-GFP mouse are also discussed.

Indexed as

Mice, TransgenicAnimalsBase SequenceCell LineGene Expression ProfilingGene LibraryGTP-Binding Protein alpha Subunits, Gi-GoHumansMiceMolecular Sequence DataPotassium Channels, Inwardly RectifyingPromoter Regions, GeneticProtein SubunitsReceptors, Metabotropic GlutamateRecombinant Fusion ProteinsRetinal Bipolar CellsGTP-Binding Protein alpha Subunits, Gi-GogustducinKir2.4 channelmetabotropic glutamate receptor 6Potassium Channels, Inwardly RectifyingProtein SubunitsReceptors, Metabotropic GlutamateRecombinant Fusion ProteinsTransducin

Identifiers

PMID18671302
PMCPMC2854669
OpenAlexW2158117070

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.