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Research Article

Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues

F Thiebaut, T Tsuruo, H Hamada, M M Gottesman, I Pastan, and M C Willingham
PNAS November 1, 1987 84 (21) 7735-7738; https://doi.org/10.1073/pnas.84.21.7735
F Thiebaut
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T Tsuruo
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H Hamada
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M M Gottesman
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I Pastan
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M C Willingham
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Abstract

Monoclonal antibody MRK16 was used to determine the location of P-glycoprotein, the product of the multidrug-resistance gene (MDR1), in normal human tissues. The protein was found to be concentrated in a small number of specific sites. Most tissues examined revealed very little P-glycoprotein. However, certain cell types in liver, pancreas, kidney, colon, and jejunum showed specific localization of P-glycoprotein. In liver, P-glycoprotein was found exclusively on the biliary canalicular front of hepatocytes and on the apical surface of epithelial cells in small biliary ductules. In pancreas, P-glycoprotein was found on the apical surface of the epithelial cells of small ductules but not larger pancreatic ducts. In kidney, P-glycoprotein was found concentrated on the apical surface of epithelial cells of the proximal tubules. Colon and jejunum both showed high levels of P-glycoprotein on the apical surfaces of superficial columnar epithelial cells. Adrenal gland showed high levels of P-glycoprotein diffusely distributed on the surface of cells in both the cortex and medulla. These results suggest that the protein has a role in the normal secretion of metabolites and certain anti-cancer drugs into bile, urine, and directly into the lumen of the gastrointestinal tract.

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Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues
F Thiebaut, T Tsuruo, H Hamada, M M Gottesman, I Pastan, M C Willingham
Proceedings of the National Academy of Sciences Nov 1987, 84 (21) 7735-7738; DOI: 10.1073/pnas.84.21.7735

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Cellular localization of the multidrug-resistance gene product P-glycoprotein in normal human tissues
F Thiebaut, T Tsuruo, H Hamada, M M Gottesman, I Pastan, M C Willingham
Proceedings of the National Academy of Sciences Nov 1987, 84 (21) 7735-7738; DOI: 10.1073/pnas.84.21.7735
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Proceedings of the National Academy of Sciences: 116 (49)
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