Cellular pathology of Niemann-Pick type C disease

Semin Cell Dev Biol. 2004 Aug;15(4):445-54. doi: 10.1016/j.semcdb.2004.03.001.

Abstract

Niemann-Pick type C (NPC) is a lysosomal storage disorder that results in the accumulation of cholesterol and sphingolipids. Mutations in the NPC1 or NPC2 gene are responsible for the disease but the precise functions of the encoded proteins remain unresolved. Recent observations have challenged the traditional concept of NPC as a primary cholesterol transport defect. This review updates the recent NPC literature, summarizing the increasing insight into the cholesterol trafficking circuits and also addressing the contribution of other lipids in the cellular pathogenesis. The importance of NPC as a model for subcellular lipid imbalance in studying more common diseases, such as Alzheimer's and cardiovascular diseases, is discussed.

Publication types

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

MeSH terms

  • Carrier Proteins / genetics
  • Cholesterol / metabolism
  • Endocytosis
  • Glycoproteins / genetics
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Lipid Metabolism
  • Membrane Glycoproteins / genetics
  • Niemann-Pick C1 Protein
  • Niemann-Pick Diseases / etiology
  • Niemann-Pick Diseases / metabolism
  • Niemann-Pick Diseases / pathology*
  • Vesicular Transport Proteins

Substances

  • Carrier Proteins
  • Glycoproteins
  • Intracellular Signaling Peptides and Proteins
  • Membrane Glycoproteins
  • NPC1 protein, human
  • NPC2 protein, human
  • Niemann-Pick C1 Protein
  • Vesicular Transport Proteins
  • Cholesterol