NPC1L1: evolution from pharmacological target to physiological sterol transporter

Arterioscler Thromb Vasc Biol. 2006 Nov;26(11):2433-8. doi: 10.1161/01.ATV.0000245791.53245.ee. Epub 2006 Sep 14.

Abstract

Niemann-Pick C1-like 1 protein (NPC1L1) was recently shown to be the molecular target of the cholesterol absorption inhibitor class of drugs, of which ezetimibe is the first widely used member. Since its discovery, NPC1L1 has also been shown to play a focal physiological role in intestinal absorption of sterols, including plant sterols and cholesterol. Evidence in support of this new metabolic pathway has been garnered not only through human, animal, and cell studies of function but also through the use of human genetics as an approach to study the association of NPC1L1 sequence variation with metabolic and drug-response phenotypes. The example of NPC1L1 shows how the elucidation of a pharmacological target can serve as a means to gain understanding of a key physiological pathway.

Publication types

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

MeSH terms

  • Absorption
  • Animals
  • Anticholesteremic Agents / metabolism
  • Anticholesteremic Agents / pharmacology
  • Azetidines / metabolism
  • Azetidines / pharmacology
  • Carrier Proteins / metabolism*
  • Cholesterol, LDL / antagonists & inhibitors
  • Computational Biology
  • Ezetimibe
  • Genomics
  • Humans
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Membrane Transport Proteins / metabolism
  • Mutation
  • Sterols / metabolism*
  • Subcellular Fractions / metabolism
  • Tissue Distribution

Substances

  • Anticholesteremic Agents
  • Azetidines
  • Carrier Proteins
  • Cholesterol, LDL
  • Membrane Proteins
  • Membrane Transport Proteins
  • NPC1L1 protein, human
  • Npc1l1 protein, mouse
  • Sterols
  • Ezetimibe