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[Cancer Research 47, 3920-3928, August 1, 1987]
© 1987 American Association for Cancer Research

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Sodium Dependency of Uptake of Norepinephrine and m-Iodobenzylguanidine into Cultured Human Pheochromocytoma Cells: Evidence for Uptake-One1

Sandford Jaques, Jr.2, Michael C. Tobes3 and James C. Sisson

Division of Nuclear Medicine, Department of Internal Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan 48109

Radioiodinated m-iodobenzylguanidine (MIBG), a scintigraphic agent used in the detection of human pheochromocytomas, is thought to utilize the same uptake and retention mechanism(s) as norepinephrine (NE). Using primary cultures from 16 human pheochromocytomas, we compared the uptake of MIBG to that of NE. Two different uptake systems were identified. Both NE and MIBG were taken up by a sodium-dependent system that was characterized by: (a) temperature dependency, (b) high affinity, (c) low capacity, (d) saturability, (e) ouabain sensitivity, and (f) desmethylimipramine sensitivity. However, NE and MIBG were also taken up by a temperature-dependent, sodium-independent, apparently unsaturable system. The sodium-dependent uptake system fulfills many of the criteria for Uptake-one while the sodium-independent uptake system is most likely a passive diffusion process. Competitive inhibition studies demonstrated that NE and MIBG share a common uptake system; a concept consistent with the linear correlation between the rate of uptake of 1.0 µM NE and that of 1.0 µM MIBG (r = 0.942). At low concentrations, both NE and MIBG entered the tumor cells primarily by the sodium-dependent uptake system. Differential expression of the sodium-dependent and sodium-independent uptake systems, between different tumor cells, appears to be responsible for the variations of the kinetic parameters for both NE and MIBG. These studies provide the first direct characterization of a NE uptake mechanism in human pheochromocytoma cells.

1 This investigation was supported by American Cancer Society Grant PDT-182, and by USPHS, NIH, National Institute of Arthritis, Metabolism and Digestive Diseases Grant AM-21477.

2 To whom requests for reprints should be addressed.

3 Present address: AT&T Bell Laboratories, Medical Diagnostic Systems, 480 Red Hill Rd., Middletown, NJ 07733.

Received 4/17/86. Revised 4/22/87. Accepted 5/ 4/87.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1987 by the American Association for Cancer Research.