Mutation (D472Y) in the type 3 repeat domain of cartilage oligomeric matrix protein affects its early vesicle trafficking in endoplasmic reticulum and induces apoptosis

Am J Pathol. 2003 Jul;163(1):101-10. doi: 10.1016/S0002-9440(10)63634-6.

Abstract

Cartilage oligomeric matrix protein (COMP) is a large pentameric extracellular glycoprotein found in cartilage, tendon, and synovium, and plays structural roles in cartilage as the fifth member of the thrombospondin family. Familial mutations in type 3 repeats of COMP are known to cause pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (EDM1). Although such mutations induce enlarged rough endoplasmic reticulum (rER) as a morphological change, the metabolic trafficking of mutated COMP remains unclear. In transfected COS7 cells, wild-type COMP was rapidly secreted into culture medium, while the great majority of COMP with the type 3 repeats mutation (D472Y) remained in the cells and a small portion of mutated COMP was secreted. This finding was followed up with a confocal study with an antibody specific to COMP, which demonstrated mutated COMP tightly associated with abnormally enlarged rER. Phosphorylated eIF2alpha, an ER stress protein, was expressed as a pathological reaction in virtually all COS7 cells expressing mutated but not wild-type COMP. Moreover, COS7 cells expressing mutated COMP exhibited significantly more apoptotic reaction than those expressing wild-type COMP. Pathological accumulation of COMP in rER and apoptosis in COS7 cells that were induced by the mutation (D472Y) in COMP imply that COMP mutations play a role in the pathogenesis of PSACH.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Achondroplasia / genetics
  • Achondroplasia / metabolism
  • Animals
  • Apoptosis / physiology*
  • COS Cells
  • Cartilage Oligomeric Matrix Protein
  • Chondrocytes / cytology
  • Chondrocytes / metabolism
  • DNA Fragmentation
  • Endoplasmic Reticulum / metabolism*
  • Extracellular Matrix Proteins / genetics*
  • Extracellular Matrix Proteins / metabolism*
  • Glycoproteins / genetics*
  • Glycoproteins / metabolism*
  • Golgi Apparatus / metabolism
  • Hexosaminidases / metabolism
  • Humans
  • In Situ Nick-End Labeling
  • Knee Joint / anatomy & histology
  • Matrilin Proteins
  • Mice
  • Point Mutation*
  • Protein Transport*
  • Staurosporine / metabolism
  • Transport Vesicles / metabolism*

Substances

  • Cartilage Oligomeric Matrix Protein
  • Extracellular Matrix Proteins
  • Glycoproteins
  • Matn1 protein, mouse
  • Matrilin Proteins
  • TSP5 protein, human
  • Hexosaminidases
  • Staurosporine