ZFIN ID: ZDB-PUB-110110-31
Cartilage ultrastructure in proteoglycan-deficient zebrafish mutants brings to light new candidate genes for human skeletal disorders
Wiweger, M.I., Avramut, C.M., de Andrea, C.E., Prins, F.A., Koster, A.J., Ravelli, R.B., and Hogendoorn, P.C.
Date: 2011
Source: The Journal of pathology   223(4): 531-542 (Journal)
Registered Authors: Wiweger, Malgorzata
Keywords: bone, cartilage, electron microscopy, glycans, osteochondroma, skeletal dysplasia, zebrafish
MeSH Terms:
  • Animals
  • Bone Diseases, Developmental/genetics*
  • Bone Diseases, Developmental/metabolism
  • Bone Diseases, Developmental/pathology
  • Cartilage/metabolism
  • Cartilage/ultrastructure*
  • Cell Membrane/ultrastructure
  • Chondrocytes/ultrastructure
  • Disease Models, Animal
  • Extracellular Matrix/metabolism
  • Extracellular Matrix/ultrastructure
  • Genetic Association Studies
  • Glycosaminoglycans/analysis
  • Inclusion Bodies/ultrastructure
  • Intercellular Junctions/ultrastructure
  • Microscopy, Electron
  • Osteogenesis/genetics
  • Proteoglycans/deficiency*
  • Zebrafish
PubMed: 21294126 Full text @ J. Pathol.
Proteoglycans are molecules consisting of protein cores onto which sugar chains, i.e., glycosaminoglycans (GAGs) such as heparan or chondroitin sulphates, are attached. Proteoglycans are produced by nearly all cells, and once secreted they become a major component of the extracellular matrix. Cartilage is particularly rich in proteoglycans, and changes in the structure and composition of GAGs have been found in osteochondromas and osteoarthritis. The zebrafish (Danio rerio) exhibits fast development, a growth plate-like organization of its craniofacial skeleton and an availability of various mutants, making it a powerful model for the study of human skeletal disorders with unknown aetiology. We analysed skeletons from five zebrafish lines with known mutations in genes involved in proteoglycan synthesis: dackel (dak/ext2), lacking heparan sulphate; hi307 (β3gat3), deficient for most GAGs; pinscher (pic/slc35b2), presenting defective sulphation of GAGs and other molecules; hi954 (uxs1), lacking Notch and most GAGs due to impaired protein xylosylation; and knypek (kny/gpc4), missing the protein core of the Glypican-4 proteoglycan. Here we show that each mutant displays different phenotypes related to: (a) cartilage morphology; (b) composition of the extracellular matrix; (c) ultrastructure of the extracellular matrix; and (d) the intracellular ultrastructure of chondrocytes, proving that sulphated GAGs orchestrate the cartilage intra- and extracellular ultrastructures. The mild phenotype of the hi307 mutant suggests that proteoglycans consisting of a protein core and a short sugar linker might suffice for proper chondrocyte stacking. Finally, knypek supports the involvement of Glypican-4 in the craniofacial phenotype of Simpson-Golabi-Behmel syndrome and suggests GPC4 as a modulator of the overgrowth phenotype that is associated with this syndrome and is primarily caused by a mutation in GPC3. Moreover, we speculate on the potential involvement of SLC35B2, β3GAT3 and UXS1 in skeletal dysplasias. This work promotes the use of zebrafish as a model of human skeletal development and associated pathologies.