Certain clinical symptoms such as hernias or joint contracture in patients with mucopolysaccharidoses (MPS) cannot be explained as direct consequences of the disturbed glycosaminoglycan metabolism. They may be related to secondary changes of connective tissue components. The glycoprotein fibronectin is a constituent of connective tissue with a high affinity to polyanions such as heparan sulfate or heparin. Fibronectin in addition is a potent stimulus for fibroblasts to migrate chemotactically. We studied this cell property in MPS fibroblasts. The chemotactic activity of all MPS types was diminished. MPS II fibroblasts were chemotactically inactive. When the cells were corrected for the lacking enzyme by adding conditioned medium from control fibroblasts, the chemotactic migration increased except for MPS type II cells. The known enzyme defect in the degradation process of glycosaminoglycans in MPS results in lysosomal storage of degradation products and in addition causes changes of other cell properties

Albini, A., Pontz, B., Mensing, H., Cantz, M., Muller, P. (1983). [Chemotactic activity of fibroblasts in mucopolysaccharidoses]. FT Chemotaktische Aktivitat von Fibroblasten bei Mukopolysaccharidosen. PAEDIATRIE UND PAEDOLOGIE, 18(3), 263-267.

[Chemotactic activity of fibroblasts in mucopolysaccharidoses]. FT Chemotaktische Aktivitat von Fibroblasten bei Mukopolysaccharidosen

Albini A;
1983

Abstract

Certain clinical symptoms such as hernias or joint contracture in patients with mucopolysaccharidoses (MPS) cannot be explained as direct consequences of the disturbed glycosaminoglycan metabolism. They may be related to secondary changes of connective tissue components. The glycoprotein fibronectin is a constituent of connective tissue with a high affinity to polyanions such as heparan sulfate or heparin. Fibronectin in addition is a potent stimulus for fibroblasts to migrate chemotactically. We studied this cell property in MPS fibroblasts. The chemotactic activity of all MPS types was diminished. MPS II fibroblasts were chemotactically inactive. When the cells were corrected for the lacking enzyme by adding conditioned medium from control fibroblasts, the chemotactic migration increased except for MPS type II cells. The known enzyme defect in the degradation process of glycosaminoglycans in MPS results in lysosomal storage of degradation products and in addition causes changes of other cell properties
Articolo in rivista - Articolo scientifico
Chemotaxis, Child, Enzymes/metabolism, Fibroblasts/enzymology, Fibronectins/pharmacology, Human Mucopolysaccharidoses/enzymology
German
1983
18
3
263
267
none
Albini, A., Pontz, B., Mensing, H., Cantz, M., Muller, P. (1983). [Chemotactic activity of fibroblasts in mucopolysaccharidoses]. FT Chemotaktische Aktivitat von Fibroblasten bei Mukopolysaccharidosen. PAEDIATRIE UND PAEDOLOGIE, 18(3), 263-267.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/215299
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