@article{3866352220454c178a2bdd0e494282ee,
title = "Soybean extracts increase cell surface ZIP4 abundance and cellular zinc levels: A potential novel strategy to enhance zinc absorption by ZIP4 targeting",
abstract = "Dietary zinc deficiency puts human health at risk, so we explored strategies for enhancing zinc absorption. In the small intestine, the zinc transporter ZIP4 functions as an essential component of zinc absorption. Overexpression of ZIP4 protein increases zinc uptake and thereby cellular zinc levels, suggesting that food components with the ability to increase ZIP4 could potentially enhance zinc absorption via the intestine. In the present study, we used mouse Hepa cells, which regulate mouse Zip4 (mZip4) in a manner indistinguishable from that in intestinal enterocytes, to screen for suitable food components that can increase the abundance of ZIP4. Using this ZIP4-targeting strategy, two such soybean extracts were identified that were specifically able to decrease mZip4 endocytosis in response to zinc. These soybean extracts also effectively increased the abundance of apically localized mZip4 in transfected polarized Caco2 and Madin-Darby canine kidney cells and, moreover, two apically localized mZip4 acrodermatitis enteropathica mutants. Soybean components were purified from one extract and soyasaponin Bb was identified as an active component that increased bothmZip4 protein abundance and zinc levels in Hepa cells. Finally, we confirmed that soyasaponin Bb is capable of enhancing cell surface endogenous human ZIP4 in human cells.Our results suggest that ZIP4 targetingmay represent a new strategy to improve zinc absorption in humans.",
keywords = "Apical membrane, Degradation, Endocytosis, Screening, Soyasaponin Bb, Zinc transporter",
author = "Ayako Hashimoto and Katsuma Ohkura and Masakazu Takahashi and Kumiko Kizu and Hiroshi Narita and Shuichi Enomoto and Yusaku Miyamae and Seiji Masuda and Masaya Nagao and Kazuhiro Irie and Hajime Ohigashi and Andrews, {Glen K.} and Taiho Kambe",
note = "Funding Information: We thank Dr Jack Kaplan (University of Illinois College of Medicine, Chicago, IL, U.S.A.) for providing MDCK FLp-In T-Rex cells. This work was supported by Grants-in-Aid for Challenging Exploratory Research and Scientific Research (B) from the Japan Society for the Promotion of Science [KAKENHI, Grant nos. 26660086 and 15H04501]; and by the Fuji Foundation for Protein Research, Central Miso Research Institute, Skylark Food Science Institute, a Yamada Bee Farm Grant for Honeybee Research, Kieikai Research Foundation, Nestl? Nutrition Council, Japan, Danone Institute of Japan for financial support of the [2010 DIJ Research Grant]; the Iijima Memorial Foundation for the Promotion of Food Science and Technology, Hokuto Foundation for Bioscience, Food Science Institute Foundation, Japan Food Chemical Research Foundation, Asahi Group Foundation and Mitsui Sumitomo Insurance Welfare Foundation (to T.K.), and by Adaptable and Seamless Technology Transfer Program (A-STEP) through Target-driven R&D, FS-Stage (Explora Research) from the Japan Science and Technology Agency (JST) [Grant nos. AS231Z00863E and AS242Z00171N] (to T.K. and M.T.). Publisher Copyright: {\textcopyright} 2015 Authors; published by Portland Press Limited.",
year = "2015",
month = dec,
day = "1",
doi = "10.1042/BJ20150862",
language = "English",
volume = "472",
pages = "183--193",
journal = "Biochemical Journal",
issn = "0264-6021",
publisher = "Portland Press Ltd.",
number = "2",
}