Involvement of lysosomal storage-induced p38 MAP kinase activation in the overproduction of nitric oxide by microglia in cathepsin D-deficient mice

Mol Cell Neurosci. 2007 Aug;35(4):573-84. doi: 10.1016/j.mcn.2007.05.002. Epub 2007 May 10.

Abstract

Nitric oxide (NO) and peroxynitrite, which are produced by activated microglia, are responsible for accelerated neurodegeneration in cathepsin D-deficient (CD-/-) mice. To elucidate the mechanisms by which microglia are initially activated in CD-/- mice, we analyzed the possible relationship between lysosomal storage and microglial activation. In CD-/- mice, the microglial NO-generating activity that was closely associated with the induction of inducible NO synthase and the cationic amino acid transporter-2 (CAT-2) coincided well with the lysosomal storage of subunit c of mitochondrial F0F1ATPase and the formation of ceroid/lipofuscin. Furthermore, activated microglia, which are often accumulating subunit c and ceroid/lipofuscin, showed proliferation activity and an activation of p38 mitogen-activated protein (MAP) kinase. In the primary cultured microglia, pepstatin A was found to enhance the generation of NO and superoxide anion radicals. In these pepstatin A-treated microglia, both an increased generation of the intracellular reactive oxygen species (ROS) and an activation of p38 MAP kinase were observed. These results suggest that the ceroid/lipofuscin which form in microglia activate the p38 MAP kinase cascade through the increased intracellular generation of ROS in CD-/- mice. The activated p38 MAP kinase cascade then promotes the expression of iNOS and CAT-2, thereby inducing the overproduction of NO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Argininosuccinate Synthase / metabolism
  • Brain / cytology
  • Cathepsin D / genetics
  • Cathepsin D / metabolism*
  • Cationic Amino Acid Transporter 2 / genetics
  • Cationic Amino Acid Transporter 2 / metabolism
  • Cell Shape
  • Cells, Cultured
  • Enzyme Activation
  • Lysosomes / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microglia / cytology
  • Microglia / metabolism*
  • Nitric Oxide / metabolism*
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / metabolism
  • Pepstatins / metabolism
  • Protease Inhibitors / metabolism
  • Rats
  • Rats, Wistar
  • Reactive Oxygen Species / metabolism
  • Tyrosine / analogs & derivatives
  • Tyrosine / metabolism
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism*

Substances

  • Cationic Amino Acid Transporter 2
  • Pepstatins
  • Protease Inhibitors
  • Reactive Oxygen Species
  • Nitric Oxide
  • 3-nitrotyrosine
  • Tyrosine
  • Nitric Oxide Synthase Type II
  • p38 Mitogen-Activated Protein Kinases
  • Cathepsin D
  • Argininosuccinate Synthase
  • pepstatin