Critical role for glycosphingolipids in Niemann-Pick disease type C

Curr Biol. 2001 Aug 21;11(16):1283-7. doi: 10.1016/s0960-9822(01)00396-7.

Abstract

Niemann-Pick type C (NPC) disease is a cholesterol lipidosis caused by mutations in NPC1 and NPC2 gene loci. Most human cases are caused by defects in NPC1, as are the spontaneously occurring NPC diseases in mice and cats. NPC1 protein possesses a sterol-sensing domain and has been localized to vesicles that are believed to facilitate the recycling of unesterified cholesterol from late endosomes/lysosomes to the ER and Golgi. In addition to accumulating cholesterol, NPC1-deficient cells also accumulate gangliosides and other glycosphingolipids (GSLs), and neuropathological abnormalities in NPC disease closely resemble those seen in primary gangliosidoses. These findings led us to hypothesize that NPC1 may also function in GSL homeostasis. To evaluate this possibility, we treated murine and feline NPC models with N-butyldeoxynojirimycin (NB-DNJ), an inhibitor of glucosylceramide synthase, a pivotal enzyme in the early GSL synthetic pathway. Treated animals showed delayed onset of neurological dysfunction, increased average life span (in mice), and reduced ganglioside accumulation and accompanying neuropathological changes. These results are consistent with our hypothesis and with GSLs being centrally involved in the pathogenesis of NPC disease, and they suggest that drugs inhibiting GSL synthesis could have a similar ameliorating effect on the human disorder.

Publication types

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

MeSH terms

  • 1-Deoxynojirimycin / analogs & derivatives*
  • 1-Deoxynojirimycin / therapeutic use*
  • Age Factors
  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cats
  • Cerebellum / cytology
  • Cerebellum / drug effects
  • Disease Models, Animal
  • Enzyme Inhibitors / therapeutic use
  • Glycoside Hydrolase Inhibitors
  • Glycosphingolipids / metabolism*
  • Humans
  • Immunohistochemistry
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Niemann-Pick Diseases / drug therapy*
  • Niemann-Pick Diseases / metabolism*

Substances

  • Carrier Proteins
  • Enzyme Inhibitors
  • Glycoside Hydrolase Inhibitors
  • Glycosphingolipids
  • Membrane Glycoproteins
  • NPC1 protein, human
  • 1-Deoxynojirimycin
  • miglustat