Neurodegeneration in the Niemann-Pick C mouse: glial involvement

Neuroscience. 2002;109(3):437-50. doi: 10.1016/s0306-4522(01)00517-6.

Abstract

A mouse model of Niemann-Pick type C disease has been found that exhibits neuropathology similar to the human condition. There is an age-related neurodegeneration in several brain regions and a lack of myelin in the corpus callosum in these mice. The purpose of the present study was to examine the Niemann-Pick mouse and determine whether: (1) microglia and astrocytes exhibit ultrastructural pathology similar to that found in neurons; (2) nerve fiber number is reduced when the myelin sheath is absent; and (3) the lysosomal hydrolase, cathepsin-D, is involved in the neurodegenerative process. Using light and electron microscopic methods, and immunocytochemistry, Niemann-Pick and control animals were examined at several ages. Cathepsin-D content was semi-quantitatively measured in neurons and glial cells in brain regions known to exhibit neurodegeneration, as was the density of glial fibrillary acidic protein-labeled astrocytes. The Niemann-Pick mouse exhibited: (1) an age-related increase in inclusion bodies in microglia and astrocytes, similar to that observed within neurons; (2) an almost complete absence of myelin in the corpus callosum by 7-8 weeks of age, along with a 30% reduction in the number of corpus callosum axons; (3) a mild age-related increase in cathepsin-D content within nerve cells in many brain regions. However, the cathepsin-D elevation was greatest in microglial cells; (4) an age-related increase in the number of microglial cells containing intense cathepsin-D immunoreactivity in both the thalamus and cerebellum. Both of these brain regions have been shown previously to exhibit an age-related loss of neurons; and (5) an increase in the number of reactive astrocytes immunostained for glial fibrillary acidic protein, especially in the thalamus and cerebellum. These data indicate that glial cells are a major target for pathology in the Niemann-Pick mouse. The lack of myelin within the corpus callosum may be related to the loss of nerve fibers in this structure. The increase in cathepsin-D-laden microglial cells, in brain regions previously shown to undergo neurodegeneration, is consistent with a role for microglia in the phagocytosis of dead neurons and in actively contributing to the neurodegenerative process. The activation of astrocytes in regions that undergo neurodegeneration is also consistent with a role for these glial cells in the neurodegenerative process.

Publication types

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

MeSH terms

  • Animals
  • Brain / pathology*
  • Brain / physiopathology
  • Brain / ultrastructure
  • Cathepsin D / metabolism*
  • Cell Count
  • Cell Size / physiology
  • Corpus Callosum / metabolism
  • Corpus Callosum / pathology
  • Corpus Callosum / ultrastructure
  • Disease Models, Animal
  • Female
  • Immunohistochemistry
  • Inclusion Bodies / metabolism
  • Inclusion Bodies / pathology
  • Inclusion Bodies / ultrastructure
  • Intracellular Signaling Peptides and Proteins
  • Male
  • Mice
  • Mice, Neurologic Mutants
  • Microglia / metabolism
  • Microglia / pathology
  • Microglia / ultrastructure
  • Microscopy, Electron
  • Nerve Fibers, Myelinated / metabolism
  • Nerve Fibers, Myelinated / pathology*
  • Nerve Fibers, Myelinated / ultrastructure
  • Neuroglia / metabolism
  • Neuroglia / pathology*
  • Neuroglia / ultrastructure
  • Niemann-Pick C1 Protein
  • Niemann-Pick Diseases / metabolism
  • Niemann-Pick Diseases / pathology*
  • Niemann-Pick Diseases / physiopathology
  • Proteins / genetics
  • Proteins / metabolism*
  • Wallerian Degeneration / metabolism
  • Wallerian Degeneration / pathology
  • Wallerian Degeneration / physiopathology

Substances

  • Intracellular Signaling Peptides and Proteins
  • Niemann-Pick C1 Protein
  • Npc1 protein, mouse
  • Proteins
  • Cathepsin D