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Expression and Functionality of Anti-Human Immunodeficiency Virus and Anticancer Drug Uptake Transporters in Immune Cells
Almost all drugs used in anti-human immunodeficiency virus (HIV)-1 and anticancer therapies require membrane proteins to get into the cell to develop their proper activity. Nevertheless, little is known regarding the expression and activity of specific carriers involved in the uptake of these drugs...
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Published in: | The Journal of pharmacology and experimental therapeutics 2008-02, Vol.324 (2), p.558-567 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Almost all drugs used in anti-human immunodeficiency virus (HIV)-1 and anticancer therapies require membrane proteins to get
into the cell to develop their proper activity. Nevertheless, little is known regarding the expression and activity of specific
carriers involved in the uptake of these drugs in immune cells. Here, we assessed the mRNA levels, protein expression profile,
and activity of the gene families SLC28 (coding for concentrative nucleoside transporters, hCNT1â3), SLC29 (equilibrative nucleoside transporters, hENT1â2), and SLC22 (organic cation transporters, hOCT1â3 and hOCTN1â2). Both hENTs and hCNT2 were abundant in primary lymphocytes, with a preferential
activity of hENT1. A significant up-regulation in hENTs expression (100-fold) and activity (30-fold) was seen under stimulation
of primary T lymphocytes. In contrast, monocytes, monocyte-derived macrophages (MDMs), and immature monocyte-derived dendritic
cells predominantly expressed hCNT3, a functional transporter in MDMs. Finally, in immune cells, hOCTs showed a more heterogeneous
expression profile and a lower activity than human nucleoside transporters (hNTs), although up-regulation of hOCTs also occurred
upon lymphocyte activation. Overall, the expression and activity of most of the studied transporters emphasize their relevance
in relation to anti-HIV and anticancer therapies. The identification of the transporter involved in each specific drug uptake
in immune cells could help to optimize pharmacological therapeutic responses. |
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ISSN: | 0022-3565 1521-0103 |
DOI: | 10.1124/jpet.107.131482 |