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Review ArticleReview Article

Xenobiotic, Bile Acid, and Cholesterol Transporters: Function and Regulation

Curtis D. Klaassen and Lauren M. Aleksunes
Pharmacological Reviews March 2010, 62 (1) 1-96; DOI: https://doi.org/10.1124/pr.109.002014
Curtis D. Klaassen
Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas
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Lauren M. Aleksunes
Department of Pharmacology, Toxicology, and Therapeutics, University of Kansas Medical Center, Kansas City, Kansas
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Abstract

Transporters influence the disposition of chemicals within the body by participating in absorption, distribution, and elimination. Transporters of the solute carrier family (SLC) comprise a variety of proteins, including organic cation transporters (OCT) 1 to 3, organic cation/carnitine transporters (OCTN) 1 to 3, organic anion transporters (OAT) 1 to 7, various organic anion transporting polypeptide isoforms, sodium taurocholate cotransporting polypeptide, apical sodium-dependent bile acid transporter, peptide transporters (PEPT) 1 and 2, concentrative nucleoside transporters (CNT) 1 to 3, equilibrative nucleoside transporter (ENT) 1 to 3, and multidrug and toxin extrusion transporters (MATE) 1 and 2, which mediate the uptake (except MATEs) of organic anions and cations as well as peptides and nucleosides. Efflux transporters of the ATP-binding cassette superfamily, such as ATP-binding cassette transporter A1 (ABCA1), multidrug resistance proteins (MDR) 1 and 2, bile salt export pump, multidrug resistance-associated proteins (MRP) 1 to 9, breast cancer resistance protein, and ATP-binding cassette subfamily G members 5 and 8, are responsible for the unidirectional export of endogenous and exogenous substances. Other efflux transporters [ATPase copper-transporting β polypeptide (ATP7B) and ATPase class I type 8B member 1 (ATP8B1) as well as organic solute transporters (OST) α and β] also play major roles in the transport of some endogenous chemicals across biological membranes. This review article provides a comprehensive overview of these transporters (both rodent and human) with regard to tissue distribution, subcellular localization, and substrate preferences. Because uptake and efflux transporters are expressed in multiple cell types, the roles of transporters in a variety of tissues, including the liver, kidneys, intestine, brain, heart, placenta, mammary glands, immune cells, and testes are discussed. Attention is also placed upon a variety of regulatory factors that influence transporter expression and function, including transcriptional activation and post-translational modifications as well as subcellular trafficking. Sex differences, ontogeny, and pharmacological and toxicological regulation of transporters are also addressed. Transporters are important transmembrane proteins that mediate the cellular entry and exit of a wide range of substrates throughout the body and thereby play important roles in human physiology, pharmacology, pathology, and toxicology.

Footnotes

  • ↵1 Current affiliation: Department of Pharmacology and Toxicology, Ernest Mario School of Pharmacy and Environmental and Occupational Health Sciences Institute, Rutgers University, Piscataway, New Jersey.

  • This article is available online at http://pharmrev.aspetjournals.org.

    doi:10.1124/pr.109.002014.

  • © 2010 by The American Society for Pharmacology and Experimental Therapeutics
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Pharmacological Reviews: 62 (1)
Pharmacological Reviews
Vol. 62, Issue 1
1 Mar 2010
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Review ArticleReview Article

Xenobiotic, Bile Acid, and Cholesterol Transporters: Function and Regulation

Curtis D. Klaassen and Lauren M. Aleksunes
Pharmacological Reviews March 1, 2010, 62 (1) 1-96; DOI: https://doi.org/10.1124/pr.109.002014

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Review ArticleReview Article

Xenobiotic, Bile Acid, and Cholesterol Transporters: Function and Regulation

Curtis D. Klaassen and Lauren M. Aleksunes
Pharmacological Reviews March 1, 2010, 62 (1) 1-96; DOI: https://doi.org/10.1124/pr.109.002014
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  • Article
    • Abstract
    • I. Introduction
    • II. Transporter Families: Tissue Distribution, Subcellular Localization, and Substrates
    • III. Transporter Function in Various Tissues
    • IV. Post-Translational Regulation and Subcellular Trafficking of Transporters
    • V. Sex Differences in Transporter Expression
    • VI. Ontogeny of Transporters
    • VII. Regulation of Hepatic Transporters by Xenobiotic-Activated Transcription Factors
    • VIII. Regulation of Hepatic Transporters in Pathophysiological Conditions
    • IX. Future Directions
    • Acknowledgments.
    • Footnotes
    • References
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