Recent insights into the function and regulation of the bile salt export pump (ABCB11)

被引:34
|
作者
Stieger, Bruno [1 ]
机构
[1] Univ Zurich Hosp, Div Clin Pharmacol & Toxicol, Dept Med, CH-8091 Zurich, Switzerland
关键词
bile formation; cholestasis; inherited disease; liver; polymorphisms; RECURRENT INTRAHEPATIC CHOLESTASIS; ATP-BINDING-CASSETTE; URSODEOXYCHOLIC ACID; APICAL MEMBRANE; MUTATIONS; EXPRESSION; TRANSPORTERS; DRUG; PROTEIN; BSEP;
D O I
10.1097/MOL.0b013e32832b677c
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
Purpose of review Generation of bile is an important function of the liver. Its impairment can be caused by inherited mutations or by acquired factors and leads to cholestasis. Bile salts are an important constituent of bile and are secreted by the bile salt export pump (BSEP) from hepatocytes. Recent findings Significant progress was made in the understanding of mechanisms and consequences of malfunctioning BSEP. This information was gained from extensive characterization of patients with inherited BSEP deficiency and the subsequent characterization of the identified mutations in heterologous expression systems. Furthermore and importantly, clinical evidence shows that patients with severe BSEP deficiency are at risk to develop hepatocellular carcinoma. Bile salts are now recognized to be important in the modulation of whole body energy homeostasis. Because BSEP is the rate-limiting step in hepatocellular bile salt transport, it controls the spill over of bile salts into the systemic circulation. Therefore, an indirect role of BSEP in energy homeostasis becomes more and more likely. Summary In summary, knowledge on the physiologic and pathophysiologic role of BSEP is rapidly progressing. It can be anticipated that the next major step in better understanding BSEP should come from information on structure-function relationship. However, given the difficulty in structure determination of mammalian transporters, this will require major efforts.
引用
收藏
页码:176 / 181
页数:6
相关论文
共 50 条
  • [21] THE PRESENCE OF A TRUNCATING MUTATION IN ABCB11 ABROGATES THE BENEFICIAL EFFECT OF A RESIDUAL FUNCTION MUTATION ON THE COURSE OF SEVERE BILE SALT EXPORT PUMP DEFICIENCY
    Felzen, Antonia
    van Wessel, Daan
    Thompson, Richard J.
    Gonzales, Emmanuel M.
    Jankowska, Irena
    Shneider, Benjamin L.
    Sokal, Etienne
    Grammatikopoulos, Tassos
    Kadaristiana, Agustina
    Jacquemin, Emmanuel
    Spraul, Anne
    Lipinski, Patryk
    Czubkowski, Piotr
    Rock, Nathalie
    Shagrani, Mohammad
    Broering, Dieter
    Algoufi, Talal
    Mazhar, Nejat
    Nicastro, Emanuele
    Kelly, Deirdre
    Nebbia, Gabriella
    Arnell, Henrik
    Fischler, Bjorn
    Hulscher, Jan
    Serranti, Daniele
    Arikan, Cigdem
    Polat, Esra
    Debray, Dominique
    Lacaille, Florence
    Goncalves, Cristina
    Hierro, Loreto
    Bartolo, Gema Munoz
    Mozer-Glassberg, Yael
    Azaz, Amer
    Brecelj, Jernej
    Dezsofi, Antal
    Calvo, Pier Luigi
    Grabhorn, Enke, Jr.
    Hartleif, Steffen
    Van der Woerd, Wendy
    Kamath, Binita M.
    Wang, Jian-She
    Li, Liting
    Durmaz, Ozlem
    Kerkar, Nanda
    Jorgensen, Marianne Horby
    Fischer, Ryan T.
    Jimenez-Rivera, Carolina
    Alam, Seema
    Cananzi, Mara
    HEPATOLOGY, 2020, 72 : 884A - 886A
  • [22] Effects of common variation in the hepatocanalicular phosphatidylcholine transporter ABCB4 and the bile salt export pump ABCB11 on genetic cholangiocarcinoma risk
    Zimmer, Vincent
    Mihalache, Florentina
    Krawczyk, Marcin
    Simon, Bianca
    Gruenhage, Frank
    Acalovschi, Monica
    Lammert, Frank
    HEPATOLOGY, 2013, 58 : 1263A - 1264A
  • [23] Genetic Variations of the ABC Transporter Gene ABCB11 Encoding the Human Bile Salt Export Pump (BSEP) in a Japanese Population
    Kim, Su-Ryang
    Saito, Yoshiro
    Itoda, Masaya
    Maekawa, Keiko
    Kawamoto, Manabu
    Kamatani, Naoyuki
    Ozawa, Shogo
    Sawada, Jun-ichi
    DRUG METABOLISM AND PHARMACOKINETICS, 2009, 24 (03) : 277 - 281
  • [24] A COMMON POLYMORPHISM IN THE ABCB11 GENE ENCODING FOR THE BILE SALT EXPORT PUMP IS ASSOCIATED WITH PROGRESSION TO CIRRHOSIS IN HEPATITIS C INFECTION
    Iwata, Rika
    Stieger, Bruno
    Mertens, Joachim C.
    Frei, Pascal
    Braun, Julia
    Vergopoulos, Athanasios
    Sabrane, Karim
    Martin, Ina V.
    Goetze, Oliver
    Mullhaupt, Beat
    Geier, Andreas
    HEPATOLOGY, 2009, 50 (04) : 939A - 940A
  • [25] Heterologous Overexpression and Mutagenesis of the Human Bile Salt Export Pump (ABCB11) Using DREAM (Directed REcombination-Assisted Mutagenesis)
    Stindt, Jan
    Ellinger, Philipp
    Stross, Claudia
    Keitel, Verena
    Haeussinger, Dieter
    Smits, Sander H. J.
    Kubitz, Ralf
    Schmitt, Lutz
    PLOS ONE, 2011, 6 (05):
  • [26] Clathrin Adaptor Protein Complex 2 (AP2) Regulates The Internalization Of Bile Salt Export Pump (BSEP/ABCB11)
    Hayashi, Hisamitsu
    Inamura, Kaori
    Aida, Kensuke
    Sugiyama, Yuichi
    DRUG METABOLISM REVIEWS, 2010, 42 : 34 - 34
  • [27] Bile salt export pump deficiency disease: two novel, late onset, ABCB11 mutations identified by next generation sequencing
    Vitale, Giovanni
    Pirillo, Martina
    Mantovani, Vilma
    Marasco, Elena
    Aquilano, Adelia
    Gamal, Nesrine
    Francalanci, Paola
    Conti, Fabio
    Andreone, Pietro
    ANNALS OF HEPATOLOGY, 2016, 15 (05) : 795 - 800
  • [28] Chemical chaperones partially reverse the mis-processing of a BRIC2 mutant of the bile salt export pump, ABCB11
    Lam, Ping
    Soroka, Carol J.
    Boyer, James L.
    HEPATOLOGY, 2007, 46 (04) : 330A - 330A
  • [29] A common polymorphism in the ABCB11 gene encoding for the bile salt export pump is associated with progression to cirrhosis in hepatitis C (HCV) infection
    Iwata, Rika
    Stieger, Bruno
    Mertens, Joachim
    Frei, Pascal
    Braun, Julia
    Vergopoulos, Athanasios
    Sabrane, Karim
    Martin, Ina V.
    Goetze, Oliver
    Muellhaupt, Beat
    Geier, Andreas
    SWISS MEDICAL WEEKLY, 2009, 139 (35-36) : 8S - 8S
  • [30] Missense Mutations and Single Nucleotide Polymorphisms in ABCB11 Impair Bile Salt Export Pump Processing and Function or Disrupt Pre-Messenger RNA Splicing
    Byrne, Jane A.
    Strautnieks, Sandra S.
    Ihrke, Gudrun
    Pagani, Franco
    Kinsely, A. S.
    Linton, Kenneth J.
    Mieli-Vergani, Giorgina
    Thompson, Richard J.
    HEPATOLOGY, 2009, 49 (02) : 553 - 567