Evidence map›Paper›PMID 31626642›Full record

ArticlePLoS biology2019

Large-scale death of retinal astrocytes during normal development is non-apoptotic and implemented by microglia.

Vanessa M Puñal, Caitlin E Paisley, Federica S Brecha, Monica A Lee, Robin M Perelli, Jingjing Wang, Emily G O'Koren, Caroline R Ackley, Daniel R Saban, Benjamin E Reese and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Early Life Injury Alters Spinal Astrocyte Development.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  9. Development of Retinal Astroglia.Annual review of vision science · 2025
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Astrocyte Development in the Rodent.Advances in neurobiology · 2024
    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

11 authors at 2 institutions in 1 country.

Vanessa M PuñalDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID 0000-0002-2969-3993
Caitlin E PaisleyDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID 0000-0003-0623-8223
Federica S BrechaDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID 0000-0001-8984-5816
Monica A LeeDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.
Robin M PerelliDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.
Jingjing WangDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID 0000-0002-9362-0115
Emily G O'KorenDepartment of Ophthalmology, Duke University School of Medicine, Durham, North Carolina, United States of America.
Caroline R AckleyNeuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, California, United States of America.
Daniel R SabanDepartment of Ophthalmology, Duke University School of Medicine, Durham, North Carolina, United States of America.
Benjamin E ReeseNeuroscience Research Institute, University of California, Santa Barbara, Santa Barbara, California, United States of America.
Jeremy N KayDepartment of Neurobiology, Duke University School of Medicine, Durham, North Carolina, United States of America.ORCID 0000-0001-6145-1604
Duke University · USUniversity of California, Santa Barbara · US

Funding

VISION RESEARCHP30EY005722 · NEI · DUKE UNIVERSITY · PI Vadim Y Arshavsky · 1985 to 2026
$19.3M
Defining the Immune Cell Roles in Meibomian Gland Dysfunction in the Context of Ocular Surface Immune DiseasesR01EY021798 · NEI · SCHEPENS EYE RESEARCH INSTITUTE · PI SABAN, DANIEL RAPHAEL · 2012 to 2025
$5.3M
Development of Retinal Bipolar CellsR01EY019968 · NEI · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI REESE, BENJAMIN E · 2010 to 2023
$4.9M
Cellular and Molecular Dynamics of Retinal Microglial in the Context of Photoreceptor DegenerationR01EY030906 · NEI · DUKE UNIVERSITY · PI Daniel Raphael Saban · 2020 to 2026
$3.5M
Mechanisms of naturally-occurring astrocyte death during retinal developmentR01EY030611 · NEI · DUKE UNIVERSITY · PI Jeremy N Kay · 2019 to 2026
$2.7M
Molecular control of neuronal position during retinal developmentR01EY024694 · NEI · DUKE UNIVERSITY · PI KAY, JEREMY N · 2014 to 2018
$2.0M
NEI NIH HHS P30 EY005722NEI NIH HHS R01 EY019968NEI NIH HHS R01 EY024694NEI NIH HHS R01 EY030611NEI NIH HHS R01 EY030906
6 · The paper itself

Abstract

Naturally occurring cell death is a fundamental developmental mechanism for regulating cell numbers and sculpting developing organs. This is particularly true in the nervous system, where large numbers of neurons and oligodendrocytes are eliminated via apoptosis during normal development. Given the profound impact of death upon these two major cell populations, it is surprising that developmental death of another major cell type-the astrocyte-has rarely been studied. It is presently unclear whether astrocytes are subject to significant developmental death, and if so, how it occurs. Here, we address these questions using mouse retinal astrocytes as our model system. We show that the total number of retinal astrocytes declines by over 3-fold during a death period spanning postnatal days 5-14. Surprisingly, these astrocytes do not die by apoptosis, the canonical mechanism underlying the vast majority of developmental cell death. Instead, we find that microglia engulf astrocytes during the death period to promote their developmental removal. Genetic ablation of microglia inhibits astrocyte death, leading to a larger astrocyte population size at the end of the death period. However, astrocyte death is not completely blocked in the absence of microglia, apparently due to the ability of astrocytes to engulf each other. Nevertheless, mice lacking microglia showed significant anatomical changes to the retinal astrocyte network, with functional consequences for the astrocyte-associated vasculature leading to retinal hemorrhage. These results establish a novel modality for naturally occurring cell death and demonstrate its importance for the formation and integrity of the retinal gliovascular network.

Indexed as

AnimalsAnimals, NewbornAstrocytesBacterial ProteinsBlood VesselsCell CommunicationCell CountCell DeathDiphtheria ToxinGene Expression Regulation, DevelopmentalGenes, ReporterGlial Fibrillary Acidic ProteinLuminescent ProteinsMiceMice, Inbred C57BLMice, TransgenicBacterial ProteinsDiphtheria ToxinGlial Fibrillary Acidic Proteinglial fibrillary astrocytic protein, mouseLuminescent ProteinsPax2 protein, mousePAX2 Transcription FactorReceptor, Platelet-Derived Growth Factor alphaSox9 protein, mouseSOX9 Transcription FactorVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouseyellow fluorescent protein, Bacteria

Identifiers

PMID31626642
PMCPMC6821132
OpenAlexW2981310068

What OpenQuestion holds

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LicenceCC BY
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.