Molecular, anatomical, and biochemical events associated with neurodegeneration in mice with Niemann-Pick type C disease

Hao Li, Joyce J. Repa, Mark A. Valasek, Eduardo P. Beltroy, Stephen D. Turley, Dwight C. German, John M. Dietschy

Research output: Contribution to journalArticle

95 Scopus citations

Abstract

In Niemann-Pick type C (NPC) disease, cholesterol associated with either apoE or apoB100 is taken up by cells in all tissues, including the central nervous system, through clathrin-coated pits and becomes trapped in late endosomes and lysosomes. This study defines the functional, biochemical, and molecular events that ensue as nerve cell death occurs. In mice homozygous for a mutation in NPC1, neuromuscular dysfunction begins at 5 weeks and death occurs at 13 weeks of age. Cholesterol accumulates in every tissue in the body. Purkinje cell loss in the cerebellum begins at 3 to 4 weeks of age and is nearly complete by 11 weeks. This neurodegeneration in the cerebellum is associated with increases in the levels of mRNA for caspase 1, caspase 3, NPC2, LipA, apoE, apoD, glial fibrillary acidic protein, and tumor necrosis factor-α, but not for most target genes of the LXR nuclear receptors. The level for apoER2 is significantly reduced. These studies show there is a compensatory increase in NPC2 and LipA in an attempt to overcome the physiological defect caused by the mutation. Nevertheless, neurodegeneration proceeds utilizing apoptosis with activation of glial cells, increased apoE and apoD synthesis, and increased cholesterol turnover across the CNS.

Original languageEnglish (US)
Pages (from-to)323-333
Number of pages11
JournalJournal of neuropathology and experimental neurology
Volume64
Issue number4
DOIs
StatePublished - Apr 2005

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Keywords

  • Apolipoprotein B
  • Apolipoprotein E
  • LDLR related protein
  • LXR nuclear receptor
  • Low-density lipoprotein receptor
  • Neurodegeneration
  • Purkinje cells

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Neurology
  • Clinical Neurology
  • Cellular and Molecular Neuroscience

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