Evidence map›Paper›PMID 35152437›Full record

ArticleThe Journal of comparative neurology2022

Digital reconstruction and quantitative morphometric analysis of bipolar cells in live rat retinal slices.

Rémi Fournel, Margaret L Veruki, Espen Hartveit

Open access · hybridAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

3 authors at 1 institution in 1 country.

Rémi FournelDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID 0000-0003-2486-0307
Margaret L VerukiDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID 0000-0002-0532-144X
Espen HartveitDepartment of Biomedicine, University of Bergen, Bergen, Norway.ORCID 0000-0003-1798-1901
University of Bergen · NO

Funding

European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement 674901Horizon 2020 Framework Programme 674901Norges Forskningsråd 182743Norges Forskningsråd 189662Norges Forskningsråd 214216Norges Forskningsråd 261914
6 · The paper itself

Abstract

Bipolar cells convey signals from photoreceptors in the outer retina to amacrine and ganglion cells in the inner retina. In mammals, there are typically 10-15 types of cone bipolar cells and one type of rod bipolar cell. Different types of cone bipolar cells are thought to code and transmit different features of a complex visual stimulus, thereby generating parallel channels that uniquely filter and transform the photoreceptor outputs. Differential synaptic connectivity and expression of ligand- and voltage-gated ion channels are thought to be important mechanisms for processing and filtering visual signals. Whereas the biophysical basis for such mechanisms has been investigated more extensively in rat retina, there is a lack of quantitative morphological data necessary for advancing the structure-function correlation in this species, as recent connectomics investigations have focused on mouse retina. Here, we performed whole-cell recordings from cone and rod bipolar cells in rat retinal slices, filled the cells with fluorescent dyes, and acquired image stacks by multiphoton excitation microscopy. Following deconvolution, we performed digital reconstruction and morphometric analysis of 25 cone and 14 rod bipolar cells. Compared to previous descriptions, the extent and complexity of branching of the axon terminal was surprisingly high. By precisely quantifying the level of stratification of the axon terminals in the inner plexiform layer, we have generated a reference system for reliable classification of individual cells in future studies focused on correlating physiological and morphological properties. The implemented workflow can be extended to the development of morphologically realistic compartmental models for these neurons.

Indexed as

DendritesRetinaAnimalsAxonsMammalsMiceRatsRetinal Bipolar CellsRetinal Cone Photoreceptor Cellsbranching patterncone bipolar cellsdendritesdigital reconstructionmorphometryretina

Identifiers

PMID35152437
PMCPMC9310816
OpenAlexW4213278640

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.