Urokinase-type plasminogen activator (uPA) and its receptor (uPAR) play an important role in cell guidance and chemotaxis during normal and pathological events. uPAR is GPI-anchored and the mechanism by which it transmits intracellular polarity cues across the plasma membrane during directional sensing has not been elucidated. The constitutively recycling endocytic receptor Endo180 forms a trimolecular complex with uPAR in the presence of uPA, hence its alternate name uPAR-associated protein. Here, we demonstrate that Endo180 is a general promoter of random cell migration and has a more specific function in cell chemotaxis up a uPA gradient. Endo180 expression was demonstrated to enhance uPA-mediated filopodia production and promote rapid activation of Cdc42 and Rac. Expression of a noninternalizing Endo180 mutant revealed that promotion of random cell migration requires receptor endocytosis, whereas the chemotactic response to uPA does not. From these studies, we conclude that Endo180 is a crucial link between uPA–uPAR and setting of the internal cellular compass.
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1 September 2003
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September 02 2003
GPI-anchored uPAR requires Endo180 for rapid directional sensing during chemotaxis
Justin Sturge,
Justin Sturge
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
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Dirk Wienke,
Dirk Wienke
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
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Lucy East,
Lucy East
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
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Gareth E. Jones,
Gareth E. Jones
2The Randall Centre for Molecular Mechanisms of Cell Function, GKT School of Biomedical Sciences, New Hunt's House, London SE1 1UL, UK
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Clare M. Isacke
Clare M. Isacke
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
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Justin Sturge
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
Dirk Wienke
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
Lucy East
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
Gareth E. Jones
2The Randall Centre for Molecular Mechanisms of Cell Function, GKT School of Biomedical Sciences, New Hunt's House, London SE1 1UL, UK
Clare M. Isacke
1The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, London SW3 6JB, UK
Address correspondence to Clare M. Isacke, The Breakthrough Breast Cancer Research Centre, Institute of Cancer Research, Chester Beatty Laboratories, 237 Fulham Rd., London SW3 6JB, UK. Tel.: 44-20-7153-5510. Fax: 44-20-7153-5340. email: [email protected]
Justin Sturge and Dirk Wienke contributed equally to this work.
The online version of this article includes supplemental material.
Abbreviations used in this paper: CTLD, C-type lectin-like domain; ERK1/2, extracellular signal–regulated kinase 1/2; FNII, fibronectin type II domain; LRP, low density lipoprotein receptor–related protein; siRNA, small interfering RNA; uPA, urokinase-type plasminogen activator; uPAR, uPA receptor.
Received:
February 21 2003
Accepted:
July 11 2003
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2003
J Cell Biol (2003) 162 (5): 789–794.
Article history
Received:
February 21 2003
Accepted:
July 11 2003
Citation
Justin Sturge, Dirk Wienke, Lucy East, Gareth E. Jones, Clare M. Isacke; GPI-anchored uPAR requires Endo180 for rapid directional sensing during chemotaxis . J Cell Biol 1 September 2003; 162 (5): 789–794. doi: https://doi.org/10.1083/jcb.200302124
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