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
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 2009年 / 1791卷 / 07期
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
相关论文
共 102 条
  • [1] Reduced hepatic expression of farnesoid X receptor in hereditary cholestasis associated to mutation in ATP8B1
    Alvarez, L
    Jara, P
    Sánchez-Sabaté, E
    Hierro, L
    Larrauri, J
    Díaz, MC
    Camarena, C
    De la Vega, A
    Frauca, E
    López-Collazo, E
    Lapunzina, P
    [J]. HUMAN MOLECULAR GENETICS, 2004, 13 (20) : 2451 - 2460
  • [2] Amigo L, 1999, J LIPID RES, V40, P533
  • [3] ANDREW NM, 2004, GEMOMICS, V84, P1060
  • [4] Hepatobiliary transport: Molecular mechanisms of development and cholestasis
    Arrese, M
    Ananthananarayanan, M
    Suchy, FJ
    [J]. PEDIATRIC RESEARCH, 1998, 44 (02) : 141 - 147
  • [5] RECONSTITUTION OF ATP-DEPENDENT AMINOPHOSPHOLIPID TRANSLOCATION IN PROTEOLIPOSOMES
    AULAND, ME
    ROUFOGALIS, BD
    DEVAUX, PF
    ZACHOWSKI, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (23) : 10938 - 10942
  • [6] Evolution of substrate specificities in the P-type ATPase superfamily
    Axelsen, KB
    Palmgren, MG
    [J]. JOURNAL OF MOLECULAR EVOLUTION, 1998, 46 (01) : 84 - 101
  • [7] Aminophospholipid asymmetry: A matter of life and death
    Balasubramanian, K
    Schroit, AJ
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 2003, 65 : 701 - 734
  • [8] Capacitation-dependent reorganization of microdomains in the apical sperm head plasma membrane: Functional relationship with zona binding and the zona-induced acrosome reaction
    Boerke, A.
    Tsai, P. S.
    Garcia-Gil, N.
    Brewis, I. A.
    Gadella, B. M.
    [J]. THERIOGENOLOGY, 2008, 70 (08) : 1188 - 1196
  • [9] ASYMMETRICAL LIPID BILAYER STRUCTURE FOR BIOLOGICAL-MEMBRANES
    BRETSCHER, MS
    [J]. NATURE-NEW BIOLOGY, 1972, 236 (61): : 11 - +
  • [10] Bull LN, 1997, HEPATOLOGY, V26, P155