Regulation of Rac1 activation by the low density lipoprotein receptor-related protein.

TitleRegulation of Rac1 activation by the low density lipoprotein receptor-related protein.
Publication TypeJournal Article
Year of Publication2002
AuthorsMa Z, Thomas KS, Webb DJ, Moravec R, Salicioni AM, Mars WM, Gonias SL
JournalThe Journal of cell biology
Volume159
Issue6
Pagination1061-70
Date Published2002 Dec 23
ISSN0021-9525
KeywordsAnimals, Cell Line, Cell Movement, Culture Media, Serum-Free, Enzyme Activation, Fibroblasts, Fibronectins, Gene Expression Regulation, Enzymologic, Ligands, Low Density Lipoprotein Receptor-Related Protein-1, Mice, Mice, Knockout, Microscopy, Fluorescence, Mitogen-Activated Protein Kinases, Protein Binding, rac1 GTP-Binding Protein, Receptors, Cell Surface, Receptors, Urokinase Plasminogen Activator, Transfection, Vitronectin
AbstractThe low density lipoprotein receptor-related protein (LRP-1) binds and mediates the endocytosis of multiple ligands, transports the urokinase-type plasminogen activator receptor (uPAR) and other membrane proteins into endosomes, and binds intracellular adaptor proteins involved in cell signaling. In this paper, we show that in murine embryonic fibroblasts (MEFs) and L929 cells, LRP-1 functions as a major regulator of Rac1 activation, and that this activity depends on uPAR. LRP-1-deficient MEFs demonstrated increased Rac1 activation compared with LRP-1-expressing MEFs, and this property was reversed by expressing the VLDL receptor, a member of the same gene family as LRP-1, with overlapping ligand-binding specificity. Neutralizing the activity of LRP-1 with receptor-associated protein (RAP) increased Rac1 activation and cell migration in MEFs and L929 cells. The same parameters were unaffected by RAP in uPAR-/- MEFs, prepared from uPAR gene knockout embryos, and in uPAR-deficient LM-TK- cells. Untreated uPAR+/+ MEFs demonstrated substantially increased Rac1 activation compared with uPAR-/- MEFs. In addition to Rac1, LRP-1 suppressed activation of extracellular signal-regulated kinase (ERK) in MEFs; however, it was Rac1 (and not ERK) that was responsible for the effects of LRP-1 on MEF migration. Thus, LRP-1 regulates two signaling proteins in the same cell (Rac1 and ERK), both of which may impact on cell migration. In uPAR-negative cells, LRP-1 neutralization does not affect Rac1 activation, and other mechanisms by which LRP-1 may regulate cell migration are not unmasked.
DOI10.1083/jcb.200207070
Alternate JournalJ. Cell Biol.
PubMed ID12499359