High binding capacity of cyclophilin B to chondrocyte heparan sulfate
Experiments with 125 I-labeled cyclophilin B demonstrated the presence of high-capacity, low-affinity, NaCl-sensitive binding sites at the surface of chondrocytes.
Experiments with 125 I-labeled cyclophilin B demonstrated the presence of high-capacity, low-affinity, NaCl-sensitive binding sites at the surface of chondrocytes.
To study cyclophilin B, a protein newly identified as a secretion product of cultured chondrocytes, in the context of chondrocyte pathobiology. Cyclophilin B was purified by sequential...
Recent studies using in vitro and in vivo models have demonstrated a role for cyclophilin–CD147 interactions in the regulation of inflammatory responses in a number of diseases, including acute
Results. Cyclophilin B was present at the surface of cultured chondrocytes and within cartilage, both in cells and in the extracellular matrix, with a particularly intense staining in the superficial layer. It was
Osteoarthritis (OA) is a disease in which the pathogenesis affects the joint and its surrounding tissues. Cartilage degeneration is the main hallmark of OA, and chondrocytes within the
Binding sites at the surface of chondrocytes were characterized by Scatchard plot analysis using 125 I‐labeled cyclophilin B, and by glycosidase treatments. The release of cyclophilin B from
Heparan sulfate (HS)4 proteoglycans on the cell surface or in the extracellular matrix are involved in developmental, regeneratory, and inflammatory processes, as a consequence of their interactions
Article: High binding capacity of cyclophilin B to chondrocyte heparan sulfate proteoglycans and its release from the cell surface by matrix metalloproteinases: Possible role as a proinflammatory
Read "High binding capacity of cyclophilin B to chondrocyte heparan sulfate proteoglycans and its release from the cell surface by matrix metalloproteinases: Possible role as a proinflammatory
To elucidate how the specificity of CyPB binding is determined, we explored the relationships between the expression of these sulfotransferases and the generation of HS motifs with CyPB-binding properties.
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