Membrane Protein Research Group, Edmonton, Alberta, Canada T6G 2H7.
Mol Aspects Med. 2013 Apr-Jun;34(2-3):529-47. doi: 10.1016/j.mam.2012.05.007.
Nucleoside transport in humans is mediated by members of two unrelated protein families, the SLC28 family of cation-linked concentrative nucleoside transporters (CNTs) and the SLC29 family of energy-independent, equilibrative nucleoside transporters (ENTs). These families contain three and four members, respectively, which differ both in the stoichiometry of cation coupling and in permeant selectivity. Together, they play key roles in nucleoside and nucleobase uptake for salvage pathways of nucleotide synthesis. Moreover, they facilitate cellular uptake of several nucleoside and nucleobase drugs used in cancer chemotherapy and treatment of viral infections. Thus, the transporter content of target cells can represent a key determinant of the response to treatment. In addition, by regulating the concentration of adenosine available to cell surface receptors, nucleoside transporters modulate many physiological processes ranging from neurotransmission to cardiovascular activity. This review describes the molecular and functional properties of the two transporter families, with a particular focus on their physiological roles in humans and relevance to disease treatment.
核苷在人体内的转运是由两个不相关的蛋白家族成员介导的,即 SLC28 家族的阳离子依赖型浓缩核苷转运体(CNTs)和 SLC29 家族的能量非依赖型、平衡核苷转运体(ENTs)。这两个家族分别包含三个和四个成员,它们在阳离子偶联的计量和渗透性选择性方面存在差异。它们共同在核苷酸合成的补救途径中发挥关键作用,促进核苷和核苷碱基的摄取。此外,它们还促进了几种用于癌症化疗和病毒感染治疗的核苷和碱基药物在细胞内的摄取。因此,靶细胞的转运体含量可以代表对治疗反应的关键决定因素。此外,通过调节细胞表面受体可用的腺苷浓度,核苷转运体调节从神经传递到心血管活动等多种生理过程。本综述描述了这两个转运体家族的分子和功能特性,特别关注它们在人类中的生理作用及其与疾病治疗的相关性。