Evidence map›Paper›PMID 22061481›Full record

ArticleDevelopmental biology2012

Time-lapse imaging reveals stereotypical patterns of Drosophila midline glial migration.

Scott R Wheeler, Joseph C Pearson, Stephen T Crews

Open access · greenAbstract read
In one paragraph

Article in Developmental biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Genetics · 2019
    Review
  3. I Spy in the Developing Fly a Multitude of Ways to Die.Journal of developmental biology · 2018
    Review
  4. Article
  5. Article
  6. Netrin and Frazzled regulate presynaptic gap junctions at a Drosophila giant synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  7. Review
  8. 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.

Scott R WheelerDepartment of Biochemistry and Biophysics, Program in Molecular Biology and Biotechnology, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
Joseph C Pearson
Stephen T Crews
University of North Carolina at Chapel Hill · US

Funding

Molecular Biology of NeurogenesisR37HD025251 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CREWS, STEPHEN T · 2001 to 2010
$3.1M
Molecular Genetics of Midline Glial DevelopmentR01NS075079 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CREWS, STEPHEN T · 2011 to 2015
$1.6M
UNC Developmental Biology Training ProgramT32HD046369 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAGNUSON, TERRY R · 2005 to 2009
$1.4M
Molecular Genetics of Midline Glial DevelopmentR01NS064264 · NINDS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CREWS, STEPHEN T · 2009 to 2010
$737k
Analysis of Cis-Regulatory Mechanisms in Drosophila CNS Midline GenesF32HD061175 · NICHD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PEARSON, JOSEPH CARLISLE · 2010 to 2011
$107k
NICHD NIH HHS F32 HD061175NICHD NIH HHS R37 HD025251NICHD NIH HHS T32 HD046369NINDS NIH HHS R01 NS064264NINDS NIH HHS R01 NS075079NINDS NIH HHS R01 NS64264ORD VA R37 RD25251
6 · The paper itself

Abstract

The Drosophila CNS midline glia (MG) are multifunctional cells that ensheath and provide trophic support to commissural axons, and direct embryonic development by employing a variety of signaling molecules. These glia consist of two functionally distinct populations: the anterior MG (AMG) and posterior MG (PMG). Only the AMG ensheath axon commissures, whereas the function of the non-ensheathing PMG is unknown. The Drosophila MG have proven to be an excellent system for studying glial proliferation, cell fate, apoptosis, and axon-glial interactions. However, insight into how AMG migrate and acquire their specific positions within the axon-glial scaffold has been lacking. In this paper, we use time-lapse imaging, single-cell analysis, and embryo staining to comprehensively describe the proliferation, migration, and apoptosis of the Drosophila MG. We identified 3 groups of MG that differed in the trajectories of their initial inward migration: AMG that migrate inward and to the anterior before undergoing apoptosis, AMG that migrate inward and to the posterior to ensheath commissural axons, and PMG that migrate inward and to the anterior to contact the commissural axons before undergoing apoptosis. In a second phase of their migration, the surviving AMG stereotypically migrated posteriorly to specific positions surrounding the commissures, and their final position was correlated with their location prior to migration. Most noteworthy are AMG that migrated between the commissures from a ventral to a dorsal position. Single-cell analysis indicated that individual AMG possessed wide-ranging and elaborate membrane extensions that partially ensheathed both commissures. These results provide a strong foundation for future genetic experiments to identify mutants affecting MG development, particularly in guidance cues that may direct migration. Drosophila MG are homologous in structure and function to the glial-like cells that populate the vertebrate CNS floorplate, and study of Drosophila MG will provide useful insights into floorplate development and function.

Indexed as

Cell MovementAnimalsApoptosisAxonsCell DivisionDrosophila melanogasterEmbryonic DevelopmentEmbryo, NonmammalianMembranesModels, BiologicalNeurogliaTime-Lapse Imaging

Identifiers

PMID22061481
PMCPMC3246554
OpenAlexW2090631431

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.