Evidence map›Paper›PMID 36094265›Full record

ArticleJournal of visualized experiments : JoVE2022

Developing Drosophila melanogaster Models for Imaging and Optogenetic Control of Cardiac Function.

Elena Gracheva, Fei Wang, Abigail Matt, Hongwu Liang, Matthew Fishman, Chao Zhou

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  3. bioRxiv : the preprint server for biology · 2025
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  5. Attention LSTM U-Net model forBiomedical optics express · 2024
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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 1 institution in 1 country.

Elena GrachevaDepartment of Biomedical Engineering, Washington University in St. Louis.
Fei WangDepartment of Biomedical Engineering, Washington University in St. Louis.
Abigail MattDepartment of Biomedical Engineering, Washington University in St. Louis.
Hongwu LiangDepartment of Biomedical Engineering, Washington University in St. Louis.
Matthew FishmanDepartment of Biomedical Engineering, Washington University in St. Louis; Department of Computer Science and Engineering, Washington University in St. Louis.
Chao ZhouDepartment of Biomedical Engineering, Washington University in St. Louis; chaozhou@wustl.edu.
Washington University in St. Louis · US

Funding

High-throughput integrated live imaging and optogenetic pacing platform to assess hypoxia responsiveness in the fly heartR01HL156265 · NHLBI · WASHINGTON UNIVERSITY · PI ZHOU, CHAO · 2021 to 2024
$2.1M
High throughput optical coherence tomography (OCT)-based imaging platform for label-free, non-invasive characterization of 3D tumor spheroids.R01EB025209 · NIBIB · WASHINGTON UNIVERSITY · PI ZHOU, CHAO · 2017 to 2021
$1.4M
NHLBI NIH HHS R01 HL156265NIBIB NIH HHS R01 EB025209
6 · The paper itself

Abstract

Using Drosophila melanogaster (fruit fly) as a model organism has ensured significant progress in many areas of biological science, from cellular organization and genomic investigations to behavioral studies. Due to the accumulated scientific knowledge, in recent years, Drosophila was brought to the field of modeling human diseases, including heart disorders. The presented work describes the experimental system for monitoring and manipulating the heart function in the context of a whole live organism using red light (617 nm) and without invasive procedures. Control over the heart was achieved using optogenetic tools. Optogenetics combines the expression of light-sensitive transgenic opsins and their optical activation to regulate the biological tissue of interest. In this work, a custom integrated optical coherence tomography (OCT) imaging and optogenetic stimulation system was used to visualize and modulate the functioning D. melanogaster heart at the 3rd instar larval and early pupal developmental stages. The UAS/GAL4 dual genetic system was employed to express halorhodopsin (eNpHR2.0) and red-shifted channelrhodopsin (ReaChR), specifically in the fly heart. Details on preparing D. melanogaster for live OCT imaging and optogenetic pacing are provided. A lab-developed integration software processed the imaging data to create visual presentations and quantitative characteristics of Drosophila heart function. The results demonstrate the feasibility of initiating cardiac arrest and bradycardia caused by eNpHR2.0 activation and performing heart pacing upon ReaChR activation.

Indexed as

Drosophila melanogasterOptogeneticsAnimalsCardiovascular Physiological PhenomenaDrosophilaHeartHumans

Identifiers

PMID36094265
PMCPMC9825051
OpenAlexW4293237510

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.