Quantitative Atlas of Blood-Brain Barrier Transporters, Receptors, and Tight Junction Proteins in Rats and Common Marmoset

被引:181
作者
Hoshi, Yutaro [1 ]
Uchida, Yasuo [1 ]
Tachikawa, Masanori [1 ]
Inoue, Takashi [2 ]
Ohtsuki, Sumio [3 ]
Terasaki, Tetsuya [1 ]
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci, Div Membrane Transport & Drug Targeting, Aoba Ku, Sendai, Miyagi 9808578, Japan
[2] Cent Inst Expt Anim, Kawasaki Ku, Kawasaki, Kanagawa 2100821, Japan
[3] Kumamoto Univ, Fac Life Sci, Dept Pharmaceut Microbiol, Chuo Ku, Kumamoto 8620973, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
blood-brain barrier; membrane transporter; proteomics; multidrug resistance transporters; P-glycoprotein; receptors; tight junction; permeability; ADME; preclinical pharmacokinetics; CAPILLARY ENDOTHELIAL-CELLS; TARGETED ABSOLUTE PROTEOMICS; CANCER RESISTANCE PROTEIN; MESSENGER-RNA EXPRESSION; P-GLYCOPROTEIN; CREATINE-TRANSPORTER; CALLITHRIX-JACCHUS; GLUCOSE-TRANSPORT; NONHUMAN-PRIMATES; EFFLUX TRANSPORT;
D O I
10.1002/jps.23575
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The purpose of this study was to determine the protein amounts of blood-brain barrier (BBB) permeability-related transporters, receptors, and tight junction proteins in Sprague Dawley and Wistar rats and common marmoset, and also to investigate inter-species and inter-strain differences across rodents and primates. Quantification of target proteins in isolated brain capillaries was conducted by liquid chromatography-tandem mass spectrometry-based quantitative targeted absolute proteomics, with in silico peptide selection. Most target proteins showed inter-rodent, inter-primate species, and inter-rat strain differences of less than 2-fold. Comparison of rat and human BBB showed that P-glycoprotein, multidrug resistance-associated protein 4, monocarboxylate transporter 1, L-type amino acid transporter, and organic anion transporter 3 exhibited differences of more than two-fold in protein abundance, whereas the amounts of breast cancer resistance protein, glucose transporter 1, and insulin receptor were similar in rat and human. In contrast, the differences between marmoset and human BBB were less than 2-fold for almost all measured proteins. Thus, the molecular basis of BBB functions may be similar in marmoset and human, whereas that of rats shows significant differences. The marmoset may be a good model to access in vivo human BBB permeability characteristics, as an alternative to rat and macaque monkey. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:3343 / 3355
页数:13
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