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Current Drug Metabolism
ISSN (Print): 1389-2002
ISSN (Online): 1875-5453
VOLUME: 9
ISSUE: 2
DOI: 10.2174/138920008783571756      Price:  $58









Genuine Functions of P-Glycoprotein (ABCB1)

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Author(s): Takaharu Mizutani, Masatoshi Masuda, Emi Nakai, Kenji Furumiya, Hiroshi Togawa, Yutaka Nakamura, Yuko Kawai, Keiko Nakahira, Shigeko Shinkai and Kazuhiko Takahashi
Pages 167-174 (8)
Abstract:
P-glycoprotein (P-gp, ABCB1, MDR1) was recognized as a drug-exporting protein from cancer cells three decade ago. Apart from the multidrug transporter side effects of P-gp, normal physiological functions of P-gp have been reported. P-gp could be responsible for translocating platelet-activating factor (PAF) across the plasma membrane and PAF inhibited drug transport mediated by P-gp in cancer cells. P-gp regulated the translocation of sphingomyelin (SM) and GlcCer, and short chain C6-NBD-GlcCer was found in the apical medium of P-gp cells exclusively and not in the basolateral membrane. SM plays an important role in the esterification of cholesterol. High expression of P-gp prevents stem-cell differentiation, leading to the proliferation and amplification of this cell repertoire, and functional P-gp plays a fundamental role in regulating programmed cell death, apoptosis. The transporter function of P-gp is therefore necessary to protect cells from death. P-gp can translocate both C6-NBD-PC and C6-NBD-PE across the apical membrane. This PC translocation was also confirmed with [3H]choline radioactivity. Progesterone is not transported by P-gp, but blocks P-gp-mediated efflux of other drugs and P-gp can mediate the transport of a variety of steroids. Cells transfected with human P-gp esterified more cholesterol. P-gp might also be involved in the transport of cytokines, particularly IL-1β, IL-2, IL-4 and IFNα, out of activated normal lymphocytes into the surrounding medium. P-gp expression is also associated with a volume-activated chloride channel, thus P-gp is bifunctional with both transport and channel regulators. We also present information about P-gp polymorphism and new structural concepts, “gate” and “twist”, of the P-gp structure.
Keywords:
P-glycoprotein, ABCB1, apoptosis, sphingomyelin, PAF, ceramide
Affiliation:
Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya 467-8603 Japan.