Evidence map›Paper›PMID 28462915›Full record

ArticleNature communications2017

Developmental activities of the complement pathway in migrating neurons.

Anna Gorelik, Tamar Sapir, Rebecca Haffner-Krausz, Tsviya Olender, Trent M Woodruff, Orly Reiner

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

81 citing papers in PubMed, 1 synthesis or guideline pooled it, 122 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Redox modulation of the complement cascade contributes to synapse loss in Alzheimer's disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Differences in the Effectiveness of Uridine andPharmaceuticals (Basel, Switzerland) · 2025
    Article
  14. Article
  15. Genes & diseases · 2025
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Review

21 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

6 authors at 2 institutions in 2 countries.

Anna GorelikDepartment of Molecular Genetics, Weizmann Institute of Science, 234 Herzl St, Rehovot 7610001, Israel.
Tamar SapirDepartment of Molecular Genetics, Weizmann Institute of Science, 234 Herzl St, Rehovot 7610001, Israel.
Rebecca Haffner-KrauszDepartment of Veterinary Resources, Weizmann Institute of Science, 234 Herzl St, Rehovot 7610001, Israel.
Tsviya OlenderDepartment of Molecular Genetics, Weizmann Institute of Science, 234 Herzl St, Rehovot 7610001, Israel.
Trent M WoodruffSchool of Biomedical Sciences, University of Queensland, BNE, Brisbane, Queensland 4072, Australia.ORCID 0000-0003-1382-911X
Orly ReinerDepartment of Molecular Genetics, Weizmann Institute of Science, 234 Herzl St, Rehovot 7610001, Israel.ORCID 0000-0001-7560-9599
Weizmann Institute of Science · ILQueensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years the notion that malfunctioning of the immune system may result in developmental brain diseases has emerged. However, the role of immune molecules in the developing brain has not been well explored. The complement pathway converges to cleave C3. Here we show that key proteins in the lectin arm of this pathway, MASP1, MASP2 and C3, are expressed in the developing cortex and that neuronal migration is impaired in knockout and knockdown mice. Molecular mimics of C3 cleavage products rescue the migration defects that have been seen following knockdown of C3 or Masp2. Pharmacological activation of the downstream receptors rescue Masp2 and C3 knockdown as well as C3 knockout. Therefore, we propose that the complement pathway is functionally important in migrating neurons of the developing cortex.

Indexed as

AnimalsCell MovementCerebral CortexComplement C3Complement Pathway, Mannose-Binding LectinEmbryo, MammalianFemaleGene Expression Regulation, DevelopmentalMaleMannose-Binding Protein-Associated Serine ProteasesMiceMice, KnockoutNeuronsOligopeptidesReceptor, Anaphylatoxin C5aReceptors, G-Protein-CoupledC3a-derived anaphylatoxin receptor, mouseC5ar1 protein, mouseComplement C3Mannose-Binding Protein-Associated Serine ProteasesMASP-1 protein, mouseMASP-2 protein, mouseOligopeptidesReceptor, Anaphylatoxin C5aReceptors, G-Protein-CoupledRNA, Small Interfering

Identifiers

PMID28462915
PMCPMC5418580
OpenAlexW2611827321

What OpenQuestion holds

Textmetadata
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.