Evidence map›Paper›PMID 22046029›Full record

ArticleDisease models & mechanisms2012

Excessive activity of cathepsin K is associated with cartilage defects in a zebrafish model of mucolipidosis II.

Aaron C Petrey, Heather Flanagan-Steet, Steven Johnson, Xiang Fan, Mitche De la Rosa, Mark E Haskins, Alison V Nairn, Kelley W Moremen, Richard Steet

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Mucolipidoses Overview: Past, Present, and Future.International journal of molecular sciences · 2020
    Review
  10. Review
  11. Article
  12. Article
  13. Modeling Lysosomal Storage Diseases in the Zebrafish.Frontiers in molecular biosciences · 2020
    Review
  14. Article
  15. Characterization of mesenchymal stem cells in mucolipidosis type II (I-cell disease).Turkish journal of biology = Turk biyoloji dergisi · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
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

9 authors at 2 institutions in 1 country.

Aaron C PetreyComplex Carbohydrate Research Center, University of Georgia, Athens, GA 30602, USA.
Heather Flanagan-Steet
Steven Johnson
Xiang Fan
Mitche De la Rosa
Mark E Haskins
Alison V Nairn
Kelley W Moremen
Richard Steet
University of Georgia · USUniversity of Pennsylvania · US

Funding

ZINC DEFICIENCY &PROTEIN EXPRESSION IN RAT OLFACTORY BULBSP41RR018502 · NCRR · UNIVERSITY OF GEORGIA (UGA) · PI AZADI, PARASTOO · 2003 to 2011
$13.1M
X-LINKED SEVERE COMBINED IMMUNODEFICIENCY IN THE DOGP40RR002512 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI HASKINS, MARK E · 1985 to 2011
$7.6M
PATHOGENIC MECHANISMS OF LYSOSOMAL DISEASER01GM086524 · NIGMS · UNIVERSITY OF GEORGIA · PI STEET, RICHARD · 2009 to 2021
$4.0M
NCRR NIH HHS P40 RR002512NCRR NIH HHS P41 RR018502NCRR NIH HHS RR002512NCRR NIH HHS RR018502NIGMS NIH HHS GM086524NIGMS NIH HHS R01 GM086524
6 · The paper itself

Abstract

The severe pediatric disorder mucolipidosis II (ML-II; also known as I-cell disease) is caused by defects in mannose 6-phosphate (Man-6-P) biosynthesis. Patients with ML-II exhibit multiple developmental defects, including skeletal, craniofacial and joint abnormalities. To date, the molecular mechanisms that underlie these clinical manifestations are poorly understood. Taking advantage of a zebrafish model of ML-II, we previously showed that the cartilage morphogenesis defects in this model are associated with altered chondrocyte differentiation and excessive deposition of type II collagen, indicating that aspects of development that rely on proper extracellular matrix homeostasis are sensitive to decreases in Man-6-P biosynthesis. To further investigate the molecular bases for the cartilage phenotypes, we analyzed the transcript abundance of several genes in chondrocyte-enriched cell populations isolated from wild-type and ML-II zebrafish embryos. Increased levels of cathepsin and matrix metalloproteinase (MMP) transcripts were noted in ML-II cell populations. This increase in transcript abundance corresponded with elevated and sustained activity of several cathepsins (K, L and S) and MMP-13 during early development. Unlike MMP-13, for which higher levels of protein were detected, the sustained activity of cathepsin K at later stages seemed to result from its abnormal processing and activation. Inhibition of cathepsin K activity by pharmacological or genetic means not only reduced the activity of this enzyme but led to a broad reduction in additional protease activity, significant correction of the cartilage morphogenesis phenotype and reduced type II collagen staining in ML-II embryos. Our findings suggest a central role for excessive cathepsin K activity in the developmental aspects of ML-II cartilage pathogenesis and highlight the utility of the zebrafish system to address the biochemical underpinnings of metabolic disease.

Indexed as

AnimalsAnimals, Genetically ModifiedBase SequenceCartilageCathepsin KCollagen Type IICraniofacial AbnormalitiesDisease Models, AnimalExtracellular Matrix ProteinsHumansMannosephosphatesMucolipidosesRNA, MessengerZebrafishZebrafish ProteinsCathepsin KCollagen Type IIExtracellular Matrix Proteinsmannose-6-phosphateMannosephosphatesRNA, MessengerZebrafish Proteins

Identifiers

PMID22046029
PMCPMC3291639
OpenAlexW2134859844

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.