Evidence map›Paper›PMID 28287587›Full record

ArticleJournal of visualized experiments : JoVE2017

Analyzing Synaptic Modulation of Drosophila melanogaster Photoreceptors after Exposure to Prolonged Light.

Atsushi Sugie, Christoph Möhl, Satoko Hakeda-Suzuki, Hideaki Matsui, Takashi Suzuki, Gaia Tavosanis

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. eLife · 2024
    Article
  2. Article
  3. A Quantitative Model of Sporadic Axonal Degeneration in theThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  4. 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

6 authors at 3 institutions in 2 countries.

Atsushi SugieDepartment of Neuroscience of Disease, Center for Transdisciplinary Research, Niigata University; Brain Research Institute, Niigata University; Dendrite Differentiation, German Center for Neurodegenerative Diseases (DZNE); atsushi.sugie@bri.niigata-u.ac.jp.
Christoph MöhlImage and Data Analysis Facility, German Center for Neurodegenerative Diseases (DZNE); christoph.moehl@dzne.de.
Satoko Hakeda-SuzukiGraduate School of Life Science and Technology, Tokyo Institute of Technology (Titech).
Hideaki MatsuiDepartment of Neuroscience of Disease, Center for Transdisciplinary Research, Niigata University; Brain Research Institute, Niigata University.
Takashi SuzukiGraduate School of Life Science and Technology, Tokyo Institute of Technology (Titech).
Gaia TavosanisDendrite Differentiation, German Center for Neurodegenerative Diseases (DZNE).
German Center for Neurodegenerative Diseases · DENiigata University · JPTokyo Institute of Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The nervous system has the remarkable ability to adapt and respond to various stimuli. This neural adjustment is largely achieved through plasticity at the synaptic level. The Active Zone (AZ) is the region at the presynaptic membrane that mediates neurotransmitter release and is composed of a dense collection of scaffold proteins. AZs of Drosophila melanogaster (Drosophila) photoreceptors undergo molecular remodeling after prolonged exposure to natural ambient light. Thus the level of neuronal activity can rearrange the molecular composition of the AZ and contribute to the regulation of the functional output. Starting from the light exposure set-up preparation to the immunohistochemistry, this protocol details how to quantify the number, the spatial distribution, and the delocalization level of synaptic molecules at AZs in Drosophila photoreceptors. Using image analysis software, clusters of the GFP-fused AZ component Bruchpilot were identified for each R8 photoreceptor (R8) axon terminal. Detected Bruchpilot spots were automatically assigned to individual R8 axons. To calculate the distribution of spot frequency along the axon, we implemented a customized software plugin. Each axon's start-point and end-point were manually defined and the position of each Bruchpilot spot was projected onto the connecting line between start and end-point. Besides the number of Bruchpilot clusters, we also quantified the delocalization level of Bruchpilot-GFP within the clusters. These measurements reflect in detail the spatially resolved synaptic dynamics in a single neuron under different environmental conditions to stimuli.

Indexed as

LightAnimalsDrosophila melanogasterDrosophila ProteinsGreen Fluorescent ProteinsLuminescent AgentsPhotoreceptor Cells, InvertebratePresynaptic TerminalsProtein BindingProtein TransportSynapsesSynaptic TransmissionDrosophila ProteinsGreen Fluorescent ProteinsLuminescent Agents

Identifiers

PMID28287587
PMCPMC5408834
OpenAlexW2586975178

What OpenQuestion holds

Textmetadata
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.