Evidence map›Paper›PMID 25653313›Full record

ArticleG3 (Bethesda, Md.)2015

Comparison of larval and adult Drosophila astrocytes reveals stage-specific gene expression profiles.

Yanmei Huang, Fanny S Ng, F Rob Jackson

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Article
  3. Insects · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Astrocyte Development in the Rodent.Advances in neurobiology · 2024
    Review
  10. Article
  11. TDP-43 pathology inbioRxiv : the preprint server for biology · 2023
    Article
  12. Article
  13. Astrocyte development-More questions than answers.Frontiers in cell and developmental biology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. International journal of molecular sciences · 2020
    Review
  19. Article
  20. 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.

Yanmei HuangDepartment of Neuroscience, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111.
Fanny S NgDepartment of Neuroscience, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111.
F Rob JacksonDepartment of Neuroscience, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111 rob.jackson@tufts.edu.

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
Regulation of Astrocyte Heterogeneity and Developmental Maturation in the CNSR01MH099554 · NIMH · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB, YANG, YONGJIE · 2013 to 2017
$2.8M
Glial Cell Regulation of Circadian BehaviorR01NS065900 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2010 to 2014
$1.8M
Genetic Analysis of Glia-to-Neuron CommunicationR21NS077886 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2012 to 2013
$447k
NIMH NIH HHS R01 MH099554NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS065900NINDS NIH HHS R21 NS077886PHS HHS R21 077886
6 · The paper itself

Abstract

The analysis of adult astrocyte glial cells has revealed a remarkable heterogeneity with regard to morphology, molecular signature, and physiology. A key question in glial biology is how such heterogeneity arises during brain development. One approach to this question is to identify genes with differential astrocyte expression during development; certain genes expressed later in neural development may contribute to astrocyte differentiation. We have utilized the Drosophila model and Translating Ribosome Affinity Purification (TRAP)-RNA-seq methods to derive the genome-wide expression profile of Drosophila larval astrocyte-like cells (hereafter referred to as astrocytes) for the first time. These studies identified hundreds of larval astrocyte-enriched genes that encode proteins important for metabolism, energy production, and protein synthesis, consistent with the known role of astrocytes in the metabolic support of neurons. Comparison of the larval profile with that observed for adults has identified genes with astrocyte-enriched expression specific to adulthood. These include genes important for metabolism and energy production, translation, chromatin modification, protein glycosylation, neuropeptide signaling, immune responses, vesicle-mediated trafficking or secretion, and the regulation of behavior. Among these functional classes, the expression of genes important for chromatin modification and vesicle-mediated trafficking or secretion is overrepresented in adult astrocytes based on Gene Ontology analysis. Certain genes with selective adult enrichment may mediate functions specific to this stage or may be important for the differentiation or maintenance of adult astrocytes, with the latter perhaps contributing to population heterogeneity.

Indexed as

TranscriptomeAnimalsAstrocytesDrosophilaGenes, ReporterGenomeImmunohistochemistryLarvaLife Cycle StagesMicroscopy, FluorescenceNervous SystemSequence Analysis, RNAastrocyteDrosophilatranslational profilingvesicle trafficking and secretion

Identifiers

PMID25653313
PMCPMC4390571

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Registered trials

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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.