Evidence map›Paper›PMID 30136399›Full record

ArticleDevelopmental neurobiology2018

Glial Cell Expansion Coincides with Neural Circuit Formation in the Developing Auditory Brainstem.

Ashley N Brandebura, Michael Morehead, Daniel T Heller, Paul Holcomb, Douglas R Kolson, Garrett Jones, Peter H Mathers, George A Spirou

Abstract read
In one paragraph

Article in Developmental neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Research square · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Distinct Cellular Profiles ofBrain sciences · 2021
    Article
  11. Review
  12. Article
  13. 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

8 authors.

Ashley N BrandeburaRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.ORCID 0000-0001-9862-0977
Michael MoreheadRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
Daniel T HellerRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
Paul HolcombRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
Douglas R KolsonRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
Garrett JonesRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
Peter H MathersRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.
George A SpirouRockefeller Neuroscience Institute, West Virginia University, Morgantown, West Virginia.

Funding

Development of the Calyx of HeldR01DC007695 · NIDCD · WEST VIRGINIA UNIVERSITY · PI GEORGE A SPIROU, HENRIQUE Prado VON GERSDORFF · 2007 to 2026
$6.2M
COBRE Transitional Center in NeuroscienceP30GM103503 · NIGMS · WEST VIRGINIA UNIVERSITY · PI SPIROU, GEORGE A · 2012 to 2014
$3.2M
Single Cell Transcriptional Characterization of a Developing Neural CircuitF31DC017080 · NIDCD · WEST VIRGINIA UNIVERSITY · PI BRANDEBURA, ASHLEY N · 2018 to 2019
$73k
NIDCD NIH HHS F31 DC017080NIDCD NIH HHS R01 DC007695NIDCD NIH HHS R01 DC007695 (GS)NIGMS NIH HHS CoBRE P30 GM103503NIGMS NIH HHS P30 GM103503
6 · The paper itself

Abstract

Neural circuit formation involves maturation of neuronal, glial and vascular cells, as well as cell proliferation and cell death. A fundamental understanding of cellular mechanisms is enhanced by quantification of cell types during key events in synapse formation and pruning and possessing qualified genetic tools for cell type-specific manipulation. Acquiring this information in turn requires validated cell markers and genetic tools. We quantified changing proportions of neurons, astrocytes, oligodendrocytes, and microglia in the medial nucleus of the trapezoid body (MNTB) during neural circuit development. Cell type-specific markers, light microscopy and 3D virtual reality software, the latter developed in our laboratory, were used to count cells within distinct cell populations at postnatal days (P)3 and P6, bracketing the period of nerve terminal growth and pruning in this system. These data revealed a change from roughly equal numbers of neurons and glia at P3 to a 1.5:1 ratio of glia to neurons at P6. PCNA and PH3 labeling revealed that proliferation of oligodendrocytes contributed to the increase in glial cell number during this timeframe. We next evaluated Cre driver lines for selectivity in labeling cell populations. En1-Cre was specific for MNTB neurons. PDGFRα-Cre and Aldh1L1-Cre, thought to be mostly specific for oligodendrocyte lineage cells and astrocytes, respectively, both labeled significant numbers of neurons, oligodendrocytes, and astrocytes and are non-specific genetic tools in this neural system.

Indexed as

AnimalsAstrocytesBrain StemCell CycleCell ProliferationMiceMicrogliaNerve Tissue ProteinsNeurogliaNeuronsOligodendrogliaNerve Tissue Proteinsastrocytegliogenesismicroglianeuronoligodendrocyte

Identifiers

PMID30136399
PMCPMC9245928

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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.