P4 ATPases: Flippases in Health and Disease

被引:100
|
作者
van der Mark, Vincent A. [1 ]
Elferink, Ronald P. J. Oude [1 ]
Paulusma, Coen C. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Tytgat Inst Liver & Intestinal Res, NL-1105 BK Amsterdam, Netherlands
来源
关键词
P-type ATPase; P4; ATPase; flippase; phospholipid; membrane asymmetry; vesicular transport; disease; ATP8B1; CDC50; FAMILIAL INTRAHEPATIC CHOLESTASIS; TRANS-GOLGI NETWORK; PUTATIVE AMINOPHOSPHOLIPID TRANSLOCASE; SALT EXPORT PUMP; KINASE-C ZETA; CANALICULAR MEMBRANE; PLASMA-MEMBRANE; BETA-SUBUNIT; ASYMMETRIC DISTRIBUTION; PHOSPHOLIPID TRANSLOCATION;
D O I
10.3390/ijms14047897
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:7897 / 7922
页数:26
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