uPARAP/Endo 180 Is Essential for Cellular Uptake of Collagen and Promotes Fibroblast Collagen Adhesion

The uptake and lysosomal degradation of collagen by fibroblasts constitute a major pathway in the turnover of connective tissue. However, the molecular mechanisms governing this pathway are poorly understood. Here, we show that the urokinase plasminogen activator receptor-associated protein (uPARAP)...

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Veröffentlicht in:The Journal of cell biology 2003-03, Vol.160 (7), p.1009-1015
Hauptverfasser: Engelholm, Lars H., List, Karin, Netzel-Arnett, Sarah, Cukierman, Edna, Mitola, David J., Aaronson, Hannah, Kjøller, Lars, Larsen, Jørgen K., Yamada, Kenneth M., Strickland, Dudley K., Holmbeck, Kenn, Danø, Keld, Birkedal-Hansen, Henning, Behrendt, Niels, Bugge, Thomas H.
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Sprache:eng
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Zusammenfassung:The uptake and lysosomal degradation of collagen by fibroblasts constitute a major pathway in the turnover of connective tissue. However, the molecular mechanisms governing this pathway are poorly understood. Here, we show that the urokinase plasminogen activator receptor-associated protein (uPARAP)/Endo180, a novel mesenchymally expressed member of the macrophage mannose receptor family of endocytic receptors, is a key player in this process. Fibroblasts from mice with a targeted deletion in the uPARAP/Endo180 gene displayed a near to complete abrogation of collagen endocytosis. Furthermore, these cells had diminished initial adhesion to a range of different collagens, as well as impaired migration on fibrillar collagen. These studies identify a central function of uPARAP/Endo180 in cellular collagen interactions.
ISSN:0021-9525
DOI:10.1083/jcb.200211091