Evidence map›Paper›PMID 26704635›Full record

ArticleNeuroscience2016

Morphological and physiological analysis of type-5 and other bipolar cells in the Mouse Retina.

C B Hellmer, Y Zhou, B Fyk-Kolodziej, Z Hu, T Ichinose

Abstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Inducible CreEReNeuro · 2026
    Article
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  5. Article
  6. Review
  7. Article
  8. Article
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  13. Article
  14. Review
  15. Article
  16. Localization of Retinal CaFrontiers in molecular neuroscience · 2019
    Article
  17. Article
  18. Functional and Morphological Analysis of OFF Bipolar Cells.Methods in molecular biology (Clifton, N.J.) · 2018
    Article
  19. 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

5 authors.

C B HellmerDepartment of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201, United States.
Y ZhouDepartment of Otolaryngology, Wayne State University School of Medicine, Detroit, MI 48201, United States.
B Fyk-KolodziejDepartment of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201, United States.
Z HuDepartment of Otolaryngology, Wayne State University School of Medicine, Detroit, MI 48201, United States.
T IchinoseDepartment of Anatomy and Cell Biology, Wayne State University School of Medicine, Detroit, MI 48201, United States; Department of Ophthalmology, Wayne State University School of Medicine, Detroit, MI 48201, United States. Electronic address: tichinos@med.wayne.edu.

Funding

MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLSR01EY020533 · NEI · WAYNE STATE UNIVERSITY · PI ICHINOSE, TOMOMI · 2011 to 2015
$1.8M
Regeneration of auditory synaptic contacts using stem cell based approachesR01DC013275 · NIDCD · WAYNE STATE UNIVERSITY · PI HU, ZHENGQING · 2014 to 2018
$1.6M
NEI NIH HHS R01 EY020533NIDCD NIH HHS R01 DC013275
6 · The paper itself

Abstract

Retinal bipolar cells are second-order neurons in the visual system, which initiate multiple image feature-based neural streams. Among more than ten types of bipolar cells, type-5 cells are thought to play a role in motion detection pathways. Multiple subsets of type-5 cells have been reported; however, detailed characteristics of each subset have not yet been elucidated. Here, we found that they exhibit distinct morphological features as well as unique voltage-gated channel expression. We have conducted electrophysiological and immunohistochemical analysis of retinal bipolar cells. We defined type-5 cells by their axon terminal ramification in the inner plexiform layer between the border of ON/OFF sublaminae and the ON choline acetyltransferase (ChAT) band. We found three subsets of type-5 cells: XBCs had the widest axon terminals that stratified at a close approximation of the ON ChAT band as well as exhibiting large voltage-gated Na(+) channel activity, type-5-1 cells had compact terminals and no Na(+) channel activity, and type-5-2 cells contained umbrella-shaped terminals as well as large voltage-gated Na(+) channel activity. Hyperpolarization-activated cyclic nucleotide-gated (HCN) currents were also evoked in all type-5 bipolar cells. We found that XBCs and type-5-2 cells exhibited larger HCN currents than type-5-1 cells. Furthermore, the former two types showed stronger HCN1 expression than the latter. Our previous observations (Ichinose et al., 2014) match the current study: low temporal tuning cells that we named 5S corresponded to 5-1 in this study, while high temporal tuning 5f cells from the previous study corresponded to 5-2 cells. Taken together, we found three subsets of type-5 bipolar cells based on their morphologies and physiological features.

Indexed as

AnimalsAxonsBlotting, WesternCholine O-AcetyltransferaseHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsImmunohistochemistryMaleMembrane PotentialsMice, Inbred C57BLPatch-Clamp TechniquesPotassium ChannelsRetinal Bipolar CellsSodium Channel BlockersSodium ChannelsTetrodotoxinTissue Culture TechniquesCholine O-AcetyltransferaseHcn1 protein, mouseHyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsPotassium ChannelsSodium Channel BlockersSodium ChannelsTetrodotoxinbipolar cellsChAT bandHCN1 channelpatch clampvoltage-gated Na(+) channel

Identifiers

PMID26704635
PMCPMC4715942

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Registered trials

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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.