Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2004-6-8
pubmed:abstractText
Cartilage oligomeric matrix protein (COMP) is a large extracellular matrix protein expressed in cartilage, ligament and tendon. Mutations in the COMP gene cause two dominantly inherited skeletal dysplasias, pseudoachondroplasia (PSACH) and Multiple Epiphyseal Dysplasia (MED/EDM1). We report on a novel point mutation D511Y in the seventh calcium-binding repeat of the COMP gene and the resulting iliac crest growth plate pathology. The PSACH iliac crest growth plate is comprised of a large region of resting chondrocytes above a narrow region composed of clusters of disorganized proliferative and hypertrophic chondrocytes. Chondrocytes in all zones show massive intracellular retention of COMP and the surrounding extracellular matrix is deficient in COMP. Moreover, the 511Y COMP mutation selectively affects type IX collagen as little is found in the growth plate matrix whereas type II collagen and aggrecan are abundant in the matrix. Chondrocyte remnants are observed in the chondrocyte clusters and dead cells are found throughout the growth plate. Apoptosis studies demonstrate an unusual pattern of TUNEL staining in the PSACH chondrocytes compared to the control growth plate. These in vivo findings support our previous observation that retention of COMP leads to chondrocyte death. These results also add to the increasing evidence that PSACH and EDM1 are rER storage diseases and that impaired linear growth and joint erosion are caused by the disruptive effect of massive amounts of COMP within the chondrocytes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0736-0266
pubmed:author
pubmed:issnType
Print
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
759-67
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15183431-Achondroplasia, pubmed-meshheading:15183431-Aggrecans, pubmed-meshheading:15183431-Apoptosis, pubmed-meshheading:15183431-Child, pubmed-meshheading:15183431-Chondrocytes, pubmed-meshheading:15183431-Collagen Type II, pubmed-meshheading:15183431-Collagen Type X, pubmed-meshheading:15183431-DNA Mutational Analysis, pubmed-meshheading:15183431-Extracellular Matrix, pubmed-meshheading:15183431-Extracellular Matrix Proteins, pubmed-meshheading:15183431-Female, pubmed-meshheading:15183431-Glycoproteins, pubmed-meshheading:15183431-Growth Plate, pubmed-meshheading:15183431-Humans, pubmed-meshheading:15183431-Ilium, pubmed-meshheading:15183431-Immunoenzyme Techniques, pubmed-meshheading:15183431-In Situ Nick-End Labeling, pubmed-meshheading:15183431-Lectins, C-Type, pubmed-meshheading:15183431-Point Mutation, pubmed-meshheading:15183431-Proteoglycans
pubmed:year
2004
pubmed:articleTitle
Chondrocyte cell death and intracellular distribution of COMP and type IX collagen in the pseudoachondroplasia growth plate.
pubmed:affiliation
Division of Genetics and Genomic Biology, The Research Institute, University of Toronto, The Hospital for Sick Children, Toronto, Canada. jacqueline.t.hecht@uth.tmc.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't