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Aggrecan and versican: two brothers close or apart

Hideto Watanabe

2022American Journal of Physiology-Cell Physiology46 citationsDOI

Abstract

Aggrecan (Acan) and versican (Vcan) are large chondroitin sulfate proteoglycans of the extracellular matrix. They share the same structural domains at both N- and C-termini. The N-terminal G1 domain binds hyaluronan (HA), forms an HA-rich matrix, and regulates HA-mediated signaling. The C-terminal G3 domain binds other extracellular matrix molecules and forms a supramolecular structure that stores transforming growth factor β (TGFβ) and bone morphogenetic proteins (BMPs) and regulates their signaling. EGF-like motifs in the G3 domain may directly act like an EGF ligand. Both Acan and Vcan are present in cartilage, intervertebral disc, brain, heart, and aorta. Their localizations are essentially reciprocal. This review describes their structural domains, expression patterns and functions, and regulation of their expression.

Topics & Concepts

VersicanAggrecanExtracellular matrixCell biologyChemistryProteoglycanChondroitin sulfateBiglycanADAMTSCartilageMatrix metalloproteinaseBiochemistryAnatomyGlycosaminoglycanDecorinBiologyMetalloproteinaseArticular cartilageMedicineThrombospondinOsteoarthritisPathologyAlternative medicineProteoglycans and glycosaminoglycans researchProtease and Inhibitor MechanismsCell Adhesion Molecules Research
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