Mouse Equilibrative Nucleoside Transporter 2 (mENT2) Transports Nucleosides and Purine Nucleobases Differing from Human and Rat ENT2(Molecular and Cell Biology)
スポンサーリンク
概要
- 論文の詳細を見る
Several mammalian nucleoside transporters have been identified at the molecular level. Human and rat equilibrative nucleoside transporter 2 (hENT2 and rENT2, respectively) was previously reported to have the dual ability of transporting both nucleosides and nucleobases. In the present study, we characterized the transport of a variety of nucleosides and nucleobases via recombinant mouse ENT2 (mENT2). Cloned mENT2 mediated the uptake of nucleosides and purine nucleobases, but not pyrimidine nucleobases. The mENT2-mediated uptake of adenosine was significantly inhibited by nucleosides and nucleobases, irrespective of purine and pyrimidine. The K_m values for the uptake of nucleosides and purine nucleobases mediated by mENT2 varied between 1.24 and 16.3 μM, and the transport clearances of adenosine and hypoxanthine via the transporter were greater than those of other substrates. Therefore, we concluded that mENT2 is nucleoside and purine nucleobase transporter, and pyrimidine nucleobases are blockers for the transporter, differing from hENT2 and rENT2 that were reported to also transport pyrimidine nucleobases.
- 2007-05-01
著者
-
Kyotani Yoji
Department Of Environmental Biochemistry Kyoto Pharmaceutical University
-
Fujimoto Sadaki
Department Of Environmental Biochemistry Kyoto Pharmaceutical University
-
Nagasawa Kazuki
Department Of Environmental Biochemistry Kyoto Pharmaceutical University
-
NAGAI Katsuhito
Department of Environmental Biochemistry, Kyoto Pharmaceutical University
-
HIFUMI Natsuko
Department of Environmental Biochemistry, Kyoto Pharmaceutical University
-
Hifumi Natsuko
Department Of Environmental Biochemistry Kyoto Pharmaceutical University
-
Nagai Katsuhito
Department Of Environmental Biochemistry Kyoto Pharmaceutical University
-
FUJIMOTO Sadaki
Department of Biochemistry I Kyoto Pharmaceutical University:Department of III Kyoto Pharmaceutical University:Department of Pharmaceutical Chemistry II Kyoto Pharmaceutical University
関連論文
- Olmesartan Inhibits Angiotensin II–Induced Migration of Vascular Smooth Muscle Cells Through Src and Mitogen-Activated Protein Kinase Pathways
- Effects of Polymorphisms of MDR1, MRP1, and MRP2 Genes on Their mRNA Expression Levels in Duodenal Enterocytes of Healthy Japanese Subjects(Biopharmacy)
- Studies on Interactions between Traditional Herbal and Western Medicines.V. Effects of Sho-saiko-to (Xiao-Cai-hu-Tang) on the Pharmacokinetics of Carbamazepine in Rats
- Production of Phytochelatins in Polygonum cuspidatum on Exposure to Copper but not to Zinc
- Contribution of the Nucleoside Transport System to Doxorubicin Transport in HL60 Cells but Not in Mononuclear Cells
- Membrane Transport and Antitumor Activity of Pirarubicin, and Comparison with Those of Doxorubicin
- Studies on Interactions between Traditional Herbal and Western Medicines. I. Effects of Sho-seiryu-to on the Pharmacokinetics of Carbamazepine in Rats
- Possibility of Contribution of Nucleoside Transport Systems to Pirarubicin Uptake by HL60 Cells but Not Mononuclear Cells
- Inhibitory Effects of Ticlopidine and Dilazep on Serum-Induced DNA Synthesis in Cultured Rat Renal Mesangial Cells
- Pharmacokinetic Interaction between Theophylline and Propentofylline in Rats
- Transport Mechanism of Pirarubicin in Human Mononuclear Cells
- Transport Mechanisms of Anthracycline Derivatives in Human Leukemia Cell Lines : Uptake of Pirarubicin, Daunorubicin and Doxorubicin by K562 and Multidrug-Resistant K562/ADM Cell
- Transport Mechanism of Anthracycline Derivatives in Human Leukemia Cell Lines : Uptake and Efflux of Daunorubicin and Doxorubicin in HL60 and Its Resistant Cells and Comparison with Those of Pirarubicin
- Pharmacokinetics of Pirarubicin in Pediatric Patients
- Inhibitory Effect of Acetylshikonin on the Activation of NADPH Oxidase in Polymorphonuclear Leukocytes in Both Whole Cell and Cell-Free Systems
- Phorbor Myristate Acetate Induces NADPH Oxidase Activity of Cytochalasin B-Primed Neutrophils through the Protein Kinase C-Independent Pathway
- Big Mitogen-Activated Protein Kinase 1 Protects Cultured Rat Aortic Smooth Muscle Cells From Oxidative Damage
- Enhancing Effect of an Acetone Extract of Zingiberis rhizoma on Rectal Absorption of Mefenamic Acid in Rats
- Abundance of Low Molecular Weight Phosphotyrosine Protein Phosphatase in the Nerve-Ending Fraction in the Brain
- Altered Levels of Oxidation and Phospholipase C Isozyme Expression in the Brains of Theanine-Administered Rats(Molecular and Cell Biology)
- Decreased Expression of Phospholipase C-β1 Protein in Endoplasmic Reticulum Stress-Loaded Neurons(Biochemistry)
- Mouse Equilibrative Nucleoside Transporter 2 (mENT2) Transports Nucleosides and Purine Nucleobases Differing from Human and Rat ENT2(Molecular and Cell Biology)
- Effect of Phosphotyrosine Proteins on Phorbol Myristate Acetate-Induced NADPH Oxidase Activation in Guinea Pig Peritoneal Polymorphonuclear Leukocytes
- Alterations of Phospholipase C Isozymes in Rat Cerebral Cortex through Hyperoxia
- The Hydroxyl Radical Formation System in Polymorphonuclear Leukocytes
- Participation of Cytosolic Protein Phosphatase in Regulation of NADPH Oxidase in Polymorphonuclear Leukocytes
- Zinc-Ion-Dependent Acid Phosphatase Exhibits Magnesium-Ion-Dependent myo-Inositol-1-phosphatase Activity
- Characterization of High- and Low-Molecular Weight Zinc-Dependent Acid Phosphatases in Bovine Liver
- Olmesartan Inhibits Angiotensin II-Induced Migration of Vascular Smooth Muscle Cells Through Src and Mitogen-Activated Protein Kinase Pathways
- Ticlopidine Inhibits Activation of Mitogen-Activated Protein Kinase by Platelet-Derived Growth Factor in Cultured Rat Renal Mesangial Cells
- Transport Mechanisms of Idarubicin, an Anthracycline Derivative, in Human Leukemia HL60 Cells and Mononuclear Cells, and Comparison with Those of Its Analogs
- Big Mitogen-Activated Protein Kinase 1 Protects Cultured Rat Aortic Smooth Muscle Cells From Oxidative Damage
- The Role of Big Mitogen-Activated Protein Kinase 1 (BMK1) / Extracellular Signal-Regulated Kinase 5 (ERK5) in the Pathogenesis and Progression of Atherosclerosis
- The Role of Big Mitogen-Activated Protein Kinase 1 (BMK1)/Extracellular Signal-Regulated Kinase 5 (ERK5) in the Pathogenesis and Progression of Atherosclerosis