Tumor necrosis factor-alpha-associated lysosomal permeabilization is cathepsin B dependent

Am J Physiol Gastrointest Liver Physiol. 2002 Oct;283(4):G947-56. doi: 10.1152/ajpgi.00151.2002.

Abstract

Cathepsin B (Cat B) is released from lysososomes during tumor necrosis factor-alpha (TNF-alpha) cytotoxic signaling in hepatocytes and contributes to cell death. Sphingosine has recently been implicated in lysosomal permeabilization and is increased in the liver by TNF-alpha. Thus the aims of this study were to examine the mechanisms involved in TNF-alpha-associated lysosomal permeabilization, especially the role of sphingosine. Confocal microscopy demonstrated Cat B-green fluorescent protein and LysoTracker Red were both released from lysosomes after treatment of McNtcp.24 cells with TNF-alpha/actinomycin D, a finding compatible with lysosomal destabilization. In contrast, endosomes labeled with Texas Red dextran remained intact, suggesting lysosomes were specifically targeted for permeabilization. LysoTracker Red was released from lysosomes in hepatocytes treated with TNF-alpha or sphingosine in Cat B(+/+) but not Cat B(-/-) hepatocytes, as assessed by a fluorescence-based assay. With the use of a calcein release assay in isolated lysosomes, sphingosine permeabilized liver lysosomes isolated from Cat B(+/+) but not Cat B(-/-) liver. C(6) ceramide did not permeabilize lysosomes. In conclusion, these data implicate a sphingosine-Cat B interaction inducing lysosomal destabilization during TNF-alpha cytotoxic signaling.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Apoptosis
  • Cathepsin B / genetics
  • Cathepsin B / physiology*
  • Cell Membrane Permeability
  • Cells, Cultured
  • Dactinomycin / pharmacology
  • Fluorescent Dyes
  • Green Fluorescent Proteins
  • Hepatocytes / metabolism
  • Hepatocytes / ultrastructure
  • Liver Neoplasms, Experimental
  • Luminescent Proteins / genetics
  • Lysosome-Associated Membrane Glycoproteins
  • Lysosomes / metabolism*
  • Membrane Glycoproteins / genetics
  • Mice
  • Mice, Knockout
  • Microscopy, Confocal
  • Microscopy, Electron
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Sphingosine / pharmacology
  • Transfection
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Antigens, CD
  • Fluorescent Dyes
  • Luminescent Proteins
  • Lysosome-Associated Membrane Glycoproteins
  • Membrane Glycoproteins
  • Recombinant Fusion Proteins
  • Tumor Necrosis Factor-alpha
  • Green Fluorescent Proteins
  • Dactinomycin
  • Cathepsin B
  • Sphingosine