Evidence map›Paper›PMID 27557572›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

In Vitro Culturing and Live Imaging of Drosophila Egg Chambers: A History and Adaptable Method.

Nathaniel C Peters, Celeste A Berg

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. EB-SUN, a new microtubule plus-end tracking protein inMolecular biology of the cell · 2024
    Article
  4. EB-SUN, a New Microtubule Plus-End Tracking Protein inbioRxiv : the preprint server for biology · 2024
    Article
  5. Article
  6. Finishing the egg.Genetics · 2024
    Article
  7. Live Imaging of Nurse Cell Behavior in Late Stages of Drosophila Oogenesis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. 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

2 authors at 1 institution in 1 country.

Nathaniel C PetersDepartment of Genome Sciences, University of Washington, 3720 15th Ave NE, Seattle, WA, 98195-5065, USA. ncpeters@uw.edu.
Celeste A BergDepartment of Genome Sciences, University of Washington, 3720 15th Ave NE, Seattle, WA, 98195-5065, USA. caberg@uw.edu.
University of Washington · US

Funding

Regulation of tubulogenesis in the Drosophila ovaryR01GM079433 · NIGMS · UNIVERSITY OF WASHINGTON · PI BERG, CELESTE A. · 2009 to 2023
$4.2M
Leica SP8 WWL Confocal MicroscopeS10OD016240 · OD · UNIVERSITY OF WASHINGTON · PI CATTERALL, WILLIAM A · 2014 to 2014
$581k
NIGMS NIH HHS R01 GM079433NIH HHS S10 OD016240
6 · The paper itself

Abstract

The development of the Drosophila egg chamber encompasses a myriad of diverse germline and somatic events, and as such, the egg chamber has become a widely used and influential developmental model. Advantages of this system include physical accessibility, genetic tractability, and amenability to microscopy and live culturing, the last of which is the focus of this chapter. To provide adequate context, we summarize the structure of the Drosophila ovary and egg chamber, the morphogenetic events of oogenesis, the history of egg-chamber live culturing, and many of the important discoveries that this culturing has afforded. Subsequently, we discuss various culturing methods that have facilitated analyses of different stages of egg-chamber development and different types of cells within the egg chamber, and we present an optimized protocol for live culturing Drosophila egg chambers.We designed this protocol for culturing late-stage Drosophila egg chambers and live imaging epithelial tube morphogenesis, but with appropriate modifications, it can be used to culture egg chambers of any stage. The protocol employs a liquid-permeable, weighted "blanket" to gently hold egg chambers against the coverslip in a glass-bottomed culture dish so the egg chambers can be imaged on an inverted microscope. This setup provides a more buffered, stable, culturing environment than previously published methods by using a larger volume of culture media, but the setup is also compatible with small volumes. This chapter should aid researchers in their efforts to culture and live-image Drosophila egg chambers, further augmenting the impressive power of this model system.

Indexed as

OogenesisAnimalsCells, CulturedDrosophilaFemaleGerm CellsMicroscopy, ConfocalMolecular ImagingOocytesOvaryOvumTime-Lapse ImagingConfocal microscopyDrosophilaEgg chamberEpithelial tube morphogenesisGermlineLive culturingLive imagingNurse cellOocyteOogenesisOvarySomatic follicle cell

Identifiers

PMID27557572
PMCPMC5244852
OpenAlexW2512483666

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.