P4 ATPases: flippases in health and disease

Int J Mol Sci. 2013 Apr 11;14(4):7897-922. doi: 10.3390/ijms14047897.

Abstract

P4 ATPases catalyze the translocation of phospholipids from the exoplasmic to the cytosolic leaflet of biological membranes, a process termed "lipid flipping". Accumulating evidence obtained in lower eukaryotes points to an important role for P4 ATPases in vesicular protein trafficking. The human genome encodes fourteen P4 ATPases (fifteen in mouse) of which the cellular and physiological functions are slowly emerging. Thus far, deficiencies of at least two P4 ATPases, ATP8B1 and ATP8A2, are the cause of severe human disease. However, various mouse models and in vitro studies are contributing to our understanding of the cellular and physiological functions of P4-ATPases. This review summarizes current knowledge on the basic function of these phospholipid translocating proteins, their proposed action in intracellular vesicle transport and their physiological role.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Biological Transport, Active / genetics
  • Disease Models, Animal
  • Genome, Human*
  • Humans
  • Metabolic Diseases / enzymology*
  • Metabolic Diseases / genetics
  • Metabolic Diseases / pathology
  • Mice
  • Phospholipid Transfer Proteins / genetics
  • Phospholipid Transfer Proteins / metabolism*
  • Phospholipids / genetics
  • Phospholipids / metabolism

Substances

  • Phospholipid Transfer Proteins
  • Phospholipids
  • ATP8a2 protein, mouse
  • Adenosine Triphosphatases
  • ATP8B1 protein, human
  • Atp8b1 protein, mouse
  • ATP8A2 protein, human