P4 ATPases - Lipid flippases and their role in disease

被引:107
|
作者
Folmer, Dineke E. [1 ]
Elferink, Ronald P. J. Oude [1 ]
Paulusma, Coen C. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, AMC Liver Ctr, NL-1105 BK Amsterdam, Netherlands
关键词
P-type ATPase; P4; ATPases; Bile formation; Cholestasis Infertility; Obesity; Membrane asymmetry; Vesicular transport; Phospholipids; Cholesterol; FAMILIAL INTRAHEPATIC CHOLESTASIS; PUTATIVE AMINOPHOSPHOLIPID TRANSLOCASE; FARNESOID-X-RECEPTOR; UNIDENTIFIED HUMAN GENES; YEAST PLASMA-MEMBRANE; CANALICULAR MEMBRANE; HEREDITARY CHOLESTASIS; SACCHAROMYCES-CEREVISIAE; PROTEIN-TRANSPORT; PHOSPHOLIPID TRANSLOCATION;
D O I
10.1016/j.bbalip.2009.02.008
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 (type 4 P-type ATPases) are multispan transmembrane proteins that have been implicated in phospholipid translocation from the exoplasmic to the cytoplasmic leaflet of biological membranes. Studies in Saccharomyces cerevisiae have indicated that P4 ATPases are important in vesicle biogenesis and are required for vesicular trafficking along several intracellular vesicular transport routes. Although little is known about mammalian P4 ATPases, some members of this subfamily appear to be associated with human disease or mouse pathophysiology. ATP8B1, a phosphatidylserine translocase, is the most extensively studied mammalian P4 ATPase. This protein is important for maintaining the detergent resistant properties of the apical membrane of the hepatocyte. Mutations in ATP8B1 give rise to severe liver disease. Furthermore, a role for Atp8b3 in mouse sperm cell capacitation has been suggested, whereas deficiency of Atp10a and Atp10d leads to insulin resistance and obesity in mice. Here we review the present status on the pathophysiological consequences of P4 ATPase deficiency. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:628 / 635
页数:8
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