Characterization of deoxyribonucleoside transport mediated by concentrative nucleoside transporters.

Human concentrative nucleoside transporters (CNTs) are responsible for cellular uptake of ribonucleosides; however, although it is important to better characterize CNT-subtype specificity to understand the systemic disposition of deoxyribonucleosides (dNs) and their analogs, the involvement of CNTs in transporting dNs is not fully understood. In this study, using COS-7 cells that transiently expressed CNT1, CNT2, or CNT3, we investigated if CNTs could transport not only ribonucleosides but also dNs, i.e., 2ʹ-deoxyadenosine (dAdo), 2ʹ-deoxyguanosine (dGuo), and 2ʹ-deoxycytidine (dCyd). The cellular uptake study demonstrated that dAdo and dGuo were taken up by CNT2 but not by CNT1. Although dCyd was taken up by CNT1, no significant uptake was detected in COS-7 cells expressing CNT2. Similarly, these dNs were transported by CNT3. The apparent K m values of their uptake were as follows: CNT1, K m ＝ 141 μM for dCyd; CNT2, K m ＝ 62.4 μM and 54.9 μM for dAdo and dGuo, respectively; CNT3, K m ＝ 14.7 μM and 34.4 μM for dGuo and dCyd, respectively. These results demonstrate that CNTs contribute not only to ribonucleoside transport but also to the transport of dNs. Moreover, our data indicated that CNT1 and CNT2 selectively transported pyrimidine and purine dNs, respectively, and CNT3 was shown to transport both pyrimidine and purine dNs. • Similar to ribonucleosides, deoxyribonucleosides are transported by CNTs. • 2ʹ-Deoxyadenosine is a substrate of CNT2 (K m = 62.4 μM). • 2ʹ-Deoxyguanosine is a substrate of both CNT2 (K m = 54.9 μM) and CNT3 (K m = 14.7 μM). • 2ʹ-Deoxycytidine is a substrate of both CNT1 (K m = 141 μM) and CNT3 (K m = 34.4 μM). [ABSTRACT FROM AUTHOR]