Brain plasmin enhances APP alpha-cleavage and Abeta degradation and is reduced in Alzheimer's disease brains

EMBO Rep. 2000 Dec;1(6):530-5. doi: 10.1093/embo-reports/kvd107.

Abstract

The proteolytic processing of amyloid precursor protein (APP) has been linked to sphingolipid-cholesterol microdomains (rafts). However, the raft proteases that may be involved in APP cleavage have not yet been identified. In this work we present evidence that the protease plasmin is restricted to rafts of cultured hippocampal neurons. We also show that plasmin increases the processing of human APP preferentially at the alpha-cleavage site, and efficiently degrades secreted amyloidogenic and non-amyloidogenic APP fragments. These results suggest that brain plasmin plays a preventive role in APP amyloidogenesis. Consistently, we show that brain tissue from Alzheimer's disease patients contains reduced levels of plasmin, implying that plasmin downregulation may cause amyloid plaque deposition accompanying sporadic Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age Factors
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / metabolism*
  • Amyloid beta-Protein Precursor / metabolism*
  • Animals
  • Blotting, Western
  • Brain / metabolism*
  • Caveolin 1
  • Caveolins / metabolism
  • Cell Line
  • Cells, Cultured
  • Fibrinolysin / chemistry
  • Fibrinolysin / metabolism*
  • G(M1) Ganglioside / metabolism
  • Hippocampus / metabolism
  • Humans
  • Membrane Microdomains / metabolism
  • Microscopy, Fluorescence
  • Middle Aged
  • Neurons / metabolism
  • Plasminogen / metabolism
  • Rats
  • Time Factors
  • Tissue Plasminogen Activator / metabolism
  • Transfection

Substances

  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Caveolin 1
  • Caveolins
  • G(M1) Ganglioside
  • Plasminogen
  • Tissue Plasminogen Activator
  • Fibrinolysin