Evidence map›Paper›PMID 22884367›Full record

ArticleCell reports2012

Target-derived matricryptins organize cerebellar synapse formation through α3β1 integrins.

Jianmin Su, Renee S Stenbjorn, Karen Gorse, Kaiwen Su, Kurt F Hauser, Sylvie Ricard-Blum, Taina Pihlajaniemi, Michael A Fox

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  6. Article
  7. Proteolysis: a key post-translational modification regulating proteoglycans.American journal of physiology. Cell physiology · 2022
    Review
  8. Article
  9. Paracrine Role for Somatostatin Interneurons in the Assembly of Perisomatic Inhibitory Synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  10. Review
  11. Article
  12. From Structure to Phenotype: Impact of Collagen Alterations on Human Health.International journal of molecular sciences · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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 at 3 institutions in 3 countries.

Jianmin SuDepartment of Anatomy and Neurobiology, Virginia Commonwealth University, Richmond, 23298, USA.
Renee S Stenbjorn
Karen Gorse
Kaiwen Su
Kurt F Hauser
Sylvie Ricard-Blum
Taina Pihlajaniemi
Michael A Fox
Virginia Commonwealth University · USInstitut de Biologie et de Chimie des Protéines · FRUniversity of Oulu · FI

Funding

VCU Neuroscience Center Core GrantP30NS047463 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI POVLISHOCK, JOHN T · 2003 to 2013
$5.0M
Regulation of nuclei-specific retinogeniculate targetingR01EY021222 · NEI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI FOX, MICHAEL A · 2011 to 2021
$3.8M
Neuron-Glia Mechanisms & Interactions Underlying Opioid Abuse-HIV-1 ComorbidityK02DA027374 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI HAUSER, KURT F · 2009 to 2018
$1.3M
NEI NIH HHS EY021222NEI NIH HHS R01 EY021222NIDA NIH HHS K02 DA027374NINDS NIH HHS NS047463NINDS NIH HHS P30 NS047463
6 · The paper itself

Abstract

Trans-synaptic organizing cues must be passed between synaptic partners for synapses to properly form. Much of our understanding of this process stems from studies at the neuromuscular junction, where target-derived growth factors, extracellular matrix (ECM) molecules, and matricryptins (proteolytically released fragments of ECM molecules) are all essential for the formation and maintenance of motor nerve terminals. While growth factors and ECM molecules also contribute to the formation of brain synapses, it remains unclear whether synaptic roles exist for matricryptins in the mammalian brain. We report that collagen XVIII and its matricryptin endostatin are generated by cerebellar Purkinje cells and are necessary for the organization of climbing fiber terminals in these neurons. Moreover, endostatin is sufficient to induce climbing fiber terminal formation in vitro by binding and signaling through α3β1 integrins. Taken together, these studies reveal roles for both matricryptins and integrins in the organization of brain synapses.

Indexed as

AnimalsCollagen Type XVIIIEndostatinsExtracellular MatrixIntegrin alpha3beta1MiceMice, KnockoutMotor NeuronsPurkinje CellsSynapsesCollagen Type XVIIIEndostatinsIntegrin alpha3beta1

Identifiers

PMID22884367
PMCPMC3432753
OpenAlexW2103091108

What OpenQuestion holds

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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.