α- 2 Macroglobulin receptor/Ldl receptor-related protein(Lrp)-dependent internalization of the urokinase receptor

Massimo Conese, Anders Nykjær, Claus M. Petersen, Ottavio Cremona, Ruggero Pardi, Peter A. Andreasen, Jørgen Gliemann, Erik I. Christensen, Francesco Blasi

Research output: Contribution to journalArticlepeer-review

Abstract

The GPI-anchored urokinase plasminogen activator receptor (uPAR) does not internalize free urokinase (uPA). On the contrary, uPAR-bound complexes of uPA with its serpin inhibitors PAI-1 (plasminogen activator inhibitor type- 1) or PN-1 (protease nexin-1) are readily internalized in several cell types. Here we address the question whether uPAR is internalized as well upon binding of uPA-serpin complexes. Both LB6 clone 19 cells, a mouse cell line transfected with the human uPAR cDNA, and the human U937 monocytic cell line, express in addition to uPAR also the endocytic α 2-macroglobulin receptor/low density lipoprotein receptor-related protein (LRP/α 2-MR) which is required to internalize uPAR-bound uPA-PAI-1 and uPA-PN-1 complexes. Downregulation of cell surface uPAR molecules in U937 cells was detected by cytofluorimetric analysis after uPA-PAI-1 and uPA-PN-1 incubation for 30 min at 37°C; this effect was blocked by preincubation with the ligand of LRP/α 2-MR, RAP (LRP/α 2-MR-associated protein), known to block the binding of the uPA complexes to LRP/α 2-MR. Downregulation correlated in time with the intracellular appearance of uPAR as assessed by confocal microscopy and immuno-electron microscopy. After 30 min incubation with uPA-PAI-1 or uPA- PN-1 (but not with free uPA), confocal microscopy showed that uPAR staining in permeabilized LB6 clone 19 cells moved from a mostly surface associated to a largely perinuclear position. This effect was inhibited by the LRP/α 2-MR RAP. Perinuclear uPAR did not represent newly synthesized nor a preexisting intracellular pool of uPAR, since this fluorescence pattern was not modified by treatment with the protein synthesis inhibitor cycloheximide, and since in LB6 clone 19 cells all of uPAR was expressed on the cell surface. Immuno- electron microscopy confirmed the plasma membrane to intracellular translocation of uPAR, and its dependence on LRP/α 2-MR in LB6 clone 19 cells only after binding to the uPA-PAI-1 complex. After 30 min incubation at 37°C with uPA-PAI-1, 93% of the specific immunogold particles were present in cytoplasmic vacuoles vs 17.6% in the case of DFP-uPA. We conclude therefore that in the process of uPA-serpin internalization, uPAR itself is internalized, and that internalization requires the LRP/α 2-MR.

Original languageEnglish
Pages (from-to)1609-1622
Number of pages14
JournalJournal of Cell Biology
Volume131
Issue number6 I
DOIs
Publication statusPublished - Dec 1995

ASJC Scopus subject areas

  • Cell Biology

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