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Am J Physiol Gastrointest Liver Physiol 294: G660-G668, 2008. First published January 3, 2008; doi:10.1152/ajpgi.00309.2007
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MUCOSAL BIOLOGY

Functional characterization of PCFT/HCP1 as the molecular entity of the carrier-mediated intestinal folate transport system in the rat model

Katsuhisa Inoue,1 Yasuhiro Nakai,1 Sayaka Ueda,1 Shunsuke Kamigaso,1 Kin-ya Ohta,1 Mai Hatakeyama,2 Yayoi Hayashi,2 Masaki Otagiri,3 and Hiroaki Yuasa1

1Department of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Nagoya City University, Nagoya; 2Department of Biopharmaceutics, College of Pharmacy, Kinjo Gakuin University, Nagoya; and 3Department of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto, Japan

Submitted 10 July 2007 ; accepted in final form 3 January 2008

Proton-coupled folate transporter/heme carrier protein 1 (PCFT/HCP1) has recently been identified as a transporter that mediates the translocation of folates across the cellular membrane by a proton-coupled mechanism and suggested to be the possible molecular entity of the carrier-mediated intestinal folate transport system. To further clarify its role in intestinal folate transport, we examined the functional characteristics of rat PCFT/HCP1 (rPCFT/HCP1) expressed in Xenopus laevis oocytes and compared with those of the carrier-mediated folate transport system in the rat small intestine evaluated by using the everted tissue sacs. rPCFT/HCP1 was demonstrated to transport folate and methotrexate more efficiently at lower acidic pH and, as evaluated at pH 5.5, with smaller Michaelis constant (Km) for the former (2.4 µM) than for the latter (5.7 µM), indicating its characteristic as a proton-coupled folate transporter that favors folate than methotrexate as substrate. rPCFT/HCP1-mediated folate transport was found to be inhibited by several but limited anionic compounds, such as sulfobromophthalein and sulfasalazine. All these characteristics of rPCFT/HCP1 were in agreement with those of carrier-mediated intestinal folate transport system, of which the Km values were 1.2 and 5.8 µM for folate and methotrexate, respectively, in the rat small intestine. Furthermore, the distribution profile of the folate transport system activity along the intestinal tract was in agreement with that of rPCFT/HCP1 mRNA. This study is the first to clone rPCFT/HCP1, and we successfully provided several lines of evidence that indicate its role as the molecular entity of the intestinal folate transport system.

methotrexate; proton-coupled folate transporter; heme carrier protein; everted sac; oocyte expression system



Address for reprint requests and other correspondence: H. Yuasa, Dept. of Biopharmaceutics, Graduate School of Pharmaceutical Sciences, Nagoya City Univ., 3-1 Tanabe-dori, Mizuho-ku, Nagoya 467-8603, Japan (e-mail: yuasa{at}phar.nagoya-cu.ac.jp)




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R. Zhao, S. H. Min, Y. Wang, E. Campanella, P. S. Low, and I. D. Goldman
A Role for the Proton-coupled Folate Transporter (PCFT-SLC46A1) in Folate Receptor-mediated Endocytosis
J. Biol. Chem., February 13, 2009; 284(7): 4267 - 4274.
[Abstract] [Full Text] [PDF]




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