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Niemann-pick C2 protein expression regulates lithogenic diet-induced gallstone formation and dietary cholesterol metabolism in mice

  • Elisa Balboab(Author)
    ,
  • Gabriela Moralesb(Author)
    ,
  • Paula Aylwinb(Author)
    ,
  • Gonzalo Carrascoa(Author)
    ,
  • Ludwig Amigob(Author)
    ,
  • Juan Castrob(Author)
  • aFundación Hospital Parroquial de San Bernardo
    ,
  • bPontificia Universidad Católica de Chile
    ,
  • cCenter FONDAP for Genome Regulation
Research Output: Contribution to journal Article Peer-review

Open access

Publication Information

Output type

Research Output: Contribution to journal Article Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 13-25 (13 pages)

Journal (Volume, Issue Number)

Lipids (Volume 47, Issue 1)

Publication milestones

  • Published - 01/01/2012

Publication status

Published - 01/01/2012

ISSN

0024-4201

External Publication IDs

  • Scopus: 84857050865
  • PubMed: 22038687

Abstract

Niemann-Pick C2 protein (NPC2) is a lysosomal soluble protein that is highly expressed in the liver; it binds to cholesterol and is involved in intracellular cholesterol trafficking, allowing the exit of lysosomal cholesterol obtained via the lipoprotein endocytic pathway. Thus, this protein may play an important role in controlling hepatic cholesterol transport and metabolism. The aim of this work was to study the relevance of NPC2 protein expression in hepatic cholesterol metabolism, biliary lipid secretion and gallstone formation by comparing NPC2 hypomorph [NPC2 (h/h)] and wild-type mice fed control, 2% cholesterol, and lithogenic diets. NPC2 (h/h) mice exhibited resistance to a diet-induced increase in plasma cholesterol levels. When consuming the chow diet, we observed increased biliary cholesterol and phospholipids secretions in NPC2 (h/h) mice. When fed the 2% cholesterol diet, NPC2 (h/h) mice exhibited low and high gallbladder bile cholesterol and phospholipid concentrations, respectively. NPC2 (h/h) mice fed with the lithogenic diet showed reduced biliary cholesterol secretion, gallbladder bile cholesterol saturation, and cholesterol crystal and gallstone formation. This work indicates that hepatic NPC2 expression is an important factor in the regulation of diet-derived cholesterol metabolism and disposal as well as in diet-induced cholesterol gallstone formation in mice.