Frontiers in Pharmacology (Feb 2016)

Cellular cholesterol distribution influences proteolytic release of the LRP-1 ectodomain

  • Bassil eDEKKY,
  • Bassil eDEKKY,
  • Amandine eWAHART,
  • Amandine eWAHART,
  • Hervé eSARTELET,
  • Hervé eSARTELET,
  • Michael eFERE,
  • Michael eFERE,
  • Michael eFERE,
  • Jean-François eANGIBOUST,
  • Jean-François eANGIBOUST,
  • Jean-François eANGIBOUST,
  • Stéphane eDEDIEU,
  • Stéphane eDEDIEU,
  • Olivier ePIOT,
  • Olivier ePIOT,
  • Olivier ePIOT,
  • Jérôme eDEVY,
  • Jérôme eDEVY,
  • Hervé eEMONARD,
  • Hervé eEMONARD

DOI
https://doi.org/10.3389/fphar.2016.00025
Journal volume & issue
Vol. 7

Abstract

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Low-Density Lipoprotein Receptor-related Protein-1 (LRP-1) is a multifunctional matricellular receptor composed of a large ligand-binding subunit (515-kDa α-chain) associated with a short trans-membrane subunit (85-kDa β-chain). LRP-1, which exhibits both endocytosis and cell signaling properties, plays a key role in tumor invasion by regulating the activity of proteinases such as matrix metalloproteinases (MMPs). LRP-1 is shed at the cell surface by proteinases such as membrane-type 1 MMP (MT1-MMP) and a disintegrin and metalloproteinase-12 (ADAM-12). Here we show by using biophysical, biochemical and cellular imaging approaches that efficient extraction of cell cholesterol and increased LRP-1 shedding occur in MDA-MB-231 breast cancer cells but not in MDA-MB-435 cells. Our data show that cholesterol is differently distributed in both cell lines; predominantly intracellularly for MDA-MB-231 cells and at the plasma membrane for MDA-MB-435 cells. This study highlights the relationship between the rate and cellular distribution of cholesterol and its impact on LRP-1 shedding modulation. Altogether, our data strongly suggest that the increase of LRP-1 shedding upon cholesterol depletion induces a higher accessibility of the sheddase substrate, ie LRP-1, at the cell surface rather than an increase of expression of the enzyme.

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