Evidence map›Paper›PMID 11733375›Full record

ArticleThe American journal of pathology2001

A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic mice.

O Jacenko, D Chan, A Franklin, S Ito, C B Underhill, J F Bateman, M R Campbell

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

14 citing papers in PubMed, 45 citations in OpenAlex.

  1. How cell migration helps immune sentinels.Frontiers in cell and developmental biology · 2022
    Review
  2. Article
  3. Extracellular matrix degradation and remodeling in development and disease.Cold Spring Harbor perspectives in biology · 2011
    Review
  4. Article
  5. Beta-catenin, cartilage, and osteoarthritis.Annals of the New York Academy of Sciences · 2010
    Review
  6. Article
  7. Article
  8. Altered endochondral ossification in collagen X mouse models leads to impaired immune responses.Developmental dynamics : an official publication of the American Association of Anatomists · 2008
    Article
  9. Heparan sulfate proteoglycans: a GAGgle of skeletal-hematopoietic regulators.Developmental dynamics : an official publication of the American Association of Anatomists · 2008
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. 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

7 authors at 5 institutions in 3 countries.

O JacenkoDepartment of Animal Biology, University of Pennsylvania School of Veterinary Medicine, Philadelphia, Pennsylvania 19104-6046, USA. jecenko@vet.upenn.edu
D Chan
A Franklin
S Ito
C B Underhill
J F Bateman
M R Campbell
University of Pennsylvania · USGeorgetown University · USHarvard University · USRoyal Children's Hospital · AUUniversity of Hong Kong · HK

Funding

MECHANISMS OF SKELETO-HEMATOPOIETIC DIFFERENTIATIONR01DK057904 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI JACENKO, OLENA · 2000 to 2008
$3.5M
MOLECULAR MECHANISMS OF SKELETOGENESISR01AR043362 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI JACENKO, OLENA · 1996 to 1999
–
NIAMS NIH HHS AR43362NIDDK NIH HHS DK57904NIDDK NIH HHS R01 DK057904
6 · The paper itself

Abstract

Collagen X transgenic (Tg) mice displayed skeleto-hematopoietic defects in tissues derived by endochondral skeletogenesis.(1) Here we demonstrate that co-expression of the transgene product containing truncated chicken collagen X with full-length mouse collagen X in a cell-free translation system yielded chicken-mouse hybrid trimers and truncated chicken homotrimers; this indicated that the mutant could assemble with endogenous collagen X and thus had potential for dominant interference. Moreover, species-specific collagen X antibodies co-localized the transgene product with endogenous collagen X to hypertrophic cartilage in growth plates and ossification centers; proliferative chondrocytes also stained diffusely. Electron microscopy revealed a disrupted hexagonal lattice network in the hypertrophic chondrocyte pericellular matrix in Tg growth plates, as well as altered mineral deposition. Ruthenium hexamine trichloride-positive aggregates, likely glycosaminoglycans (GAGs)/proteoglycans (PGs), were also dispersed throughout the chondro-osseous junction. These defects likely resulted from transgene co-localization and dominant interference with endogenous collagen X. Moreover, altered GAG/PG distribution in growth plates of both collagen X Tg and null mice was confirmed by a paucity of staining for hyaluronan and heparan sulfate PG. A provocative hypothesis links the disruption of the collagen X pericellular network and GAG/PG decompartmentalization to the potential locus for hematopoietic failure in the collagen X mice.

Indexed as

AnimalsAnimals, NewbornAntibodies, MonoclonalCartilageChickensChondrocytesCollagen Type XExtracellular MatrixGene ExpressionGenotypeGlycosaminoglycansGrowth PlateMiceMice, KnockoutMice, TransgenicMicroscopy, ElectronAntibodies, MonoclonalCollagen Type XGlycosaminoglycansProteoglycans

Identifiers

PMID11733375
PMCPMC1850580
OpenAlexW2080900460

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.