Evidence map›Paper›PMID 30647151›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2019

Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia.

Sarah R Anderson, Jianmin Zhang, Michael R Steele, Cesar O Romero, Amanda G Kautzman, Dorothy P Schafer, Monica L Vetter

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
6.0field-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

76 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
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  4. Complement in brain and eye disease: shared mechanisms, convergent pathologies, and common therapeutic opportunities.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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  16. The neuroimmune interface in retinal regeneration.Progress in retinal and eye research · 2025
    Review
  17. Article
  18. Article
  19. Article
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16 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Sarah R AndersonDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84112.
Jianmin ZhangDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84112.
Michael R SteeleDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84112.
Cesar O RomeroDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84112.
Amanda G KautzmanDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655.
Dorothy P SchaferDepartment of Neurobiology, University of Massachusetts Medical School, Worcester, Massachusetts 01655.
Monica L VetterDepartment of Neurobiology and Anatomy, University of Utah, Salt Lake City, Utah 84112, monica.vetter@neuro.utah.edu.
University of Utah · USUniversity of Massachusetts Chan Medical School · US

Funding

Microglia-dependent mechanisms governing neural circuit plasticityR01MH113743 · NIMH · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Dorothy Patricia Schafer · 2017 to 2026
$4.9M
Role of microglia during retinal neurogenesisR21EY025082 · NEI · UNIVERSITY OF UTAH · PI VETTER, MONICA L · 2015 to 2016
$410k
Microglial Crosstalk with Progenitors and Neurons during Retinal NeurogenesisF31EY025967 · NEI · UNIVERSITY OF UTAH · PI ANDERSON, SARAH ROSE · 2016 to 2017
$82k
NEI NIH HHS F31 EY025967NEI NIH HHS R21 EY025082NIMH NIH HHS R01 MH113743
6 · The paper itself

Abstract

Microglia play important roles in shaping the developing CNS, and at early stages they have been proposed to regulate progenitor proliferation, differentiation, and neuronal survival. However, these studies reveal contradictory outcomes, highlighting the complexity of these cell-cell interactions. Here, we investigate microglia function during embryonic mouse retina development, where only microglia, progenitors, and neurons are present. In both sexes, we determine that microglia primarily interact with retinal neurons and find that depletion of microglia via conditional KO of the

Indexed as

AnimalsCell CountComplement System ProteinsFemaleMacrophage Colony-Stimulating FactorMaleMice, KnockoutMicrogliaPhagocytosisRetinaRetinal Ganglion CellsComplement System ProteinsCSF1 protein, mouseMacrophage Colony-Stimulating Factorcomplementmicrogliaphagocytosisretinaretinal ganglion cell

Identifiers

PMID30647151
PMCPMC6507095
OpenAlexW2911063894

What OpenQuestion holds

Textmetadata
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.