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Biochim Biophys Acta. 2009 Jul;1791(7):671-8. doi: 10.1016/j.bbalip.2009.02.001. Epub 2009 Feb 13.

Niemann-Pick C2 (NPC2) and intracellular cholesterol trafficking.

Author information

1
Department of Nutritional Sciences and Rutgers Center for Lipid Research, Rutgers University, New Brunswick, NJ 08901, USA. storch@aesop.rutgers.edu

Abstract

Cholesterol is an important precursor for numerous biologically active molecules, and it plays a major role in membrane structure and function. Cholesterol can be endogenously synthesized or exogenously taken up via the endocytic vesicle system and subsequently delivered to post-endo/lysosomal sites including the plasma membrane and the endoplasmic reticulum. Niemann-Pick C (NPC) disease results in the accumulation of exogenously-derived cholesterol, as well as other lipids, in late endosomes and lysosomes (LE/LY). Identification of the two genes that underlie NPC disease, NPC1 and NPC2, has focused attention on the mechanisms by which lipids, in particular cholesterol, are transported out of the LE/LY compartment. This review discusses the role of the NPC2 protein in cholesterol transport, and the potential for concerted action of NPC1 and NPC2 in regulating normal intracellular cholesterol homeostasis.

PMID:
19232397
PMCID:
PMC4281484
DOI:
10.1016/j.bbalip.2009.02.001
[Indexed for MEDLINE]
Free PMC Article

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