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Perlecan Knockdown Significantly Alters Extracellular Matrix Composition and Organization During Cartilage Development.

Molecular & cellular proteomics : MCP2020Ocken AR, Ku MM, Kinzer-Ursem TL, et al.
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抄録

Perlecan is a critical proteoglycan found in the extracellular matrix (ECM) of cartilage. In healthy cartilage, perlecan regulates cartilage biomechanics and we previously demonstrated perlecan deficiency leads to reduced cellular and ECM stiffness in vivo This change in mechanics may lead to the early onset osteoarthritis seen in disorders resulting from perlecan knockdown such as Schwartz-Jampel syndrome (SJS). To identify how perlecan knockdown affects the material properties of developing cartilage, we used imaging and liquid chromatography-tandem mass spectrometry (LC-MS/MS) to study the ECM in a murine model of SJS, Hspg2C1532Y-Neo Perlecan knockdown led to defective pericellular matrix formation, whereas the abundance of bulk ECM proteins, including many collagens, increased. Post-translational modifications and ultrastructure of collagens were not significantly different; however, LC-MS/MS analysis showed more protein was secreted by Hspg2C1532Y-Neo cartilage in vitro, suggesting that the incorporation of newly synthesized ECM was impaired. In addition, glycosaminoglycan deposition was atypical, which may explain the previously observed decrease in mechanics. Overall, these findings provide insight into the influence of perlecan on functional cartilage assembly and the progression of osteoarthritis in SJS.

MeSH

AnimalsCalcium-Binding ProteinsCartilageCell Adhesion MoleculesChondrocytesChromatography, LiquidCollagen Type XDisease Models, AnimalExtracellular MatrixExtracellular Matrix ProteinsGene OntologyGlycosaminoglycansHeparan Sulfate ProteoglycansMiceMice, Inbred DBAMice, KnockoutMicroscopy, Electron, TransmissionOsteoarthritisOsteochondrodysplasiasTandem Mass Spectrometry

DOI 10.1074/mcp.ra120.001998

PMID 32381549

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