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P4 ATPases: Flippases in Health and Disease
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 ge...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645723/ https://www.ncbi.nlm.nih.gov/pubmed/23579954 http://dx.doi.org/10.3390/ijms14047897 |
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author | van der Mark, Vincent A. Oude Elferink, Ronald P.J. Paulusma, Coen C. |
author_facet | van der Mark, Vincent A. Oude Elferink, Ronald P.J. Paulusma, Coen C. |
author_sort | van der Mark, Vincent A. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3645723 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-36457232013-05-13 P4 ATPases: Flippases in Health and Disease van der Mark, Vincent A. Oude Elferink, Ronald P.J. Paulusma, Coen C. Int J Mol Sci Review 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. Molecular Diversity Preservation International (MDPI) 2013-04-11 /pmc/articles/PMC3645723/ /pubmed/23579954 http://dx.doi.org/10.3390/ijms14047897 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review van der Mark, Vincent A. Oude Elferink, Ronald P.J. Paulusma, Coen C. P4 ATPases: Flippases in Health and Disease |
title | P4 ATPases: Flippases in Health and Disease |
title_full | P4 ATPases: Flippases in Health and Disease |
title_fullStr | P4 ATPases: Flippases in Health and Disease |
title_full_unstemmed | P4 ATPases: Flippases in Health and Disease |
title_short | P4 ATPases: Flippases in Health and Disease |
title_sort | p4 atpases: flippases in health and disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3645723/ https://www.ncbi.nlm.nih.gov/pubmed/23579954 http://dx.doi.org/10.3390/ijms14047897 |
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