Evidence map›Paper›PMID 19385989›Full record

ArticleThe European journal of neuroscience2009

Differential loss and preservation of glutamate receptor function in bipolar cells in the rd10 mouse model of retinitis pigmentosa.

Theresa Puthussery, Jacqueline Gayet-Primo, Shilpi Pandey, Robert M Duvoisin, W Rowland Taylor

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

58 citing papers in PubMed, 85 citations in OpenAlex.

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  19. Non-photoreceptor Expression ofFrontiers in neuroscience · 2020
    Article
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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

5 authors at 1 institution in 1 country.

Theresa PuthusseryCasey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, Portland, OR, USA.
Jacqueline Gayet-Primo
Shilpi Pandey
Robert M Duvoisin
W Rowland Taylor
Oregon Health & Science University · US

Funding

MOLECULAR MECHANISMS OF SIGNAL TRANSDUCTION IN RETINAR01EY009534 · NEI · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI DUVOISIN, ROBERT M · 1992 to 2010
$2.8M
Biophysical limitations to signal transmission in the mammalian retinaR01EY017095 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TAYLOR, WILLIAM ROWLAND · 2006 to 2009
$1.2M
NEI NIH HHS EY017095NEI NIH HHS EY09534NEI NIH HHS R01 EY009534NEI NIH HHS R01 EY017095
6 · The paper itself

Abstract

Photoreceptor degenerations can trigger morphological alterations in second-order neurons, however, the functional implications of such changes are not well known. We conducted a longitudinal study, using whole-cell patch-clamp, immunohistochemistry and electron microscopy to correlate physiological with anatomical changes in bipolar cells of the rd10 mouse - a model of autosomal recessive retinitis pigmentosa. Rod bipolar cells (RBCs) showed progressive changes in mGluR6-induced currents with advancing rod photoreceptor degeneration. Significant changes in response amplitude and kinetics were observed as early as postnatal day (P)20, and by P45 the response amplitudes were reduced by 91%, and then remained relatively stable until 6 months. These functional changes correlated with the loss of rod photoreceptors and mGluR6 receptor expression. Moreover, we showed that RBCs make transient ectopic connections with cones during progression of the disease. At P45, ON-cone bipolar cells (ON-CBCs) retain mGluR6 responses for longer periods than the RBCs, but by about 6 months these cells also strongly downregulate mGluR6 expression. We propose that the relative longevity of mGluR6 responses in CBCs is due to the slower loss of the cones. In contrast, ionotropic glutamate receptor expression and function in OFF-CBCs remains normal at 6 months despite the loss of synaptic input from cones. Thus, glutamate receptor expression is differentially regulated in bipolar cells, with the metabotropic receptors being absolutely dependent on synaptic input. These findings define the temporal window over which bipolar cells may be receptive to photoreceptor repair or replacement.

Indexed as

Disease Models, AnimalAnimalsGlutamic AcidHumansLightLongitudinal StudiesMiceMice, Inbred C57BLPatch-Clamp TechniquesReceptors, AMPAReceptors, GlutamateRetinal Bipolar CellsRetinal Cone Photoreceptor CellsRetinal Rod Photoreceptor CellsRetinitis PigmentosaGlutamic AcidReceptors, AMPAReceptors, Glutamate

Identifiers

PMID19385989
PMCPMC2818147
OpenAlexW2094975664

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.