Evidence map›Paper›PMID 25349050›Full record

ArticleThe Journal of comparative neurology2015

Cell-specific and developmental expression of lectican-cleaving proteases in mouse hippocampus and neocortex.

C Levy, J M Brooks, J Chen, J Su, M A Fox

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. ADAMTS4 Enhances Oligodendrocyte Differentiation and Remyelination by Cleaving NG2 Proteoglycan and AttenuatingThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  5. Article
  6. Review
  7. Update on Perineuronal Net Staining WithFrontiers in integrative neuroscience · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Cerebellar plasticity and associative memories are controlled by perineuronal nets.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  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

5 authors at 2 institutions in 1 country.

C LevyVirginia Tech Carilion Research Institute, Roanoke, Virginia, 24016; Department of Biological Sciences, Virginia Tech, Blacksburg, Virginia, 24061.
J M Brooks
J Chen
J Su
M A Fox
Virginia Tech · USCarilion Clinic · US

Funding

Regulation of nuclei-specific retinogeniculate targetingR01EY021222 · NEI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI FOX, MICHAEL A · 2011 to 2021
$3.8M
NEI NIH HHS EY021222NEI NIH HHS R01 EY021222
6 · The paper itself

Abstract

Mounting evidence has demonstrated that a specialized extracellular matrix exists in the mammalian brain and that this glycoprotein-rich matrix contributes to many aspects of brain development and function. The most prominent supramolecular assemblies of these extracellular matrix glycoproteins are perineuronal nets, specialized lattice-like structures that surround the cell bodies and proximal neurites of select classes of interneurons. Perineuronal nets are composed of lecticans, a family of chondroitin sulfate proteoglycans that includes aggrecan, brevican, neurocan, and versican. These lattice-like structures emerge late in postnatal brain development, coinciding with the ending of critical periods of brain development. Despite our knowledge of the presence of lecticans in perineuronal nets and their importance in regulating synaptic plasticity, we know little about the development or distribution of the extracellular proteases that are responsible for their cleavage and turnover. A subset of a large family of extracellular proteases (called a disintegrin and metalloproteinase with thrombospondin motifs [ADAMTS]) is responsible for endogenously cleaving lecticans. We therefore explored the expression pattern of two aggrecan-degrading ADAMTS family members, ADAMTS15 and ADAMTS4, in the hippocampus and neocortex. Here, we show that both lectican-degrading metalloproteases are present in these brain regions and that each exhibits a distinct temporal and spatial expression pattern. Adamts15 mRNA is expressed exclusively by parvalbumin-expressing interneurons during synaptogenesis, whereas Adamts4 mRNA is exclusively generated by telencephalic oligodendrocytes during myelination. Thus, ADAMTS15 and ADAMTS4 not only exhibit unique cellular expression patterns but their developmental upregulation by these cell types coincides with critical aspects of neural development.

Indexed as

ADAM ProteinsADAMTS1 ProteinADAMTS4 ProteinADAMTS5 ProteinADAMTS ProteinsAnimalsGene Expression Regulation, DevelopmentalHippocampusImmunohistochemistryIn Situ Hybridization, FluorescenceInterneuronsMiceMice, Inbred C57BLNeocortexOligodendrogliaParvalbuminsADAM ProteinsADAMTS15 protein, mouseADAMTS1 ProteinAdamts1 protein, mouseADAMTS4 ProteinAdamts4 protein, mouseADAMTS5 ProteinAdamts5 protein, mouseAdamts8 protein, mouseADAMTS ProteinsParvalbuminsProcollagen N-EndopeptidaseRNA, MessengerADAMTSaggrecanaggrecanaseextracellular matrixhippocampusneocortexparvalbuminperineuronal netRRID:AB_2068506RRID:AB_221569RRID:AB_2255374RRID:AB_2278725RRID:AB_2314070RRID:AB_2314535RRID:AB_570666RRID:AB_839506RRID:AB_94270RRID:IMSR_JAX:005630RRID:IMSR_JAX:008069RRID:nif-0000-00509

Identifiers

PMID25349050
PMCPMC4304879
OpenAlexW2136795699

What OpenQuestion holds

Textmetadata
LicenceTDM
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.