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核苷转运体的新作用

Emerging Roles of Nucleoside Transporters.

作者信息

Pastor-Anglada Marçal, Pérez-Torras Sandra

机构信息

Biochemistry and Molecular Pharmacology Section, Department of Biochemistry and Molecular Biomedicine, Institute of Biomedicine (IBUB), University of Barcelona, Barcelona, Spain.

出版信息

Front Pharmacol. 2018 Jun 6;9:606. doi: 10.3389/fphar.2018.00606. eCollection 2018.

Abstract

Since human Nucleoside Transporters (hNTs) were identified by their activity as transport systems, extensive work has been done to fully characterize them at the molecular and physiological level. Many efforts have been addressed to the identification of their selectivity for natural substrates and nucleoside analogs used to treat several diseases. hNTs belong to two different gene families, and , encoding human Concentrative Nucleoside Transporters (hCNTs) and human Equilibrative Nucleoside Transporters (hENTs), respectively. hCNTs and hENTs are integral membrane proteins, albeit structurally unrelated. Both families share common features as substrate selectivity and often tissue localization. This apparent biological redundancy may anticipate some different roles for hCNTs and hENTs in cell physiology. Thus, hENTs may have a major role in maintaining nucleoside homeostasis, whereas hCNTs could contribute to nucleoside sensing and signal transduction. In this sense, the ascription of hCNT1 to a transceptor reinforces this hypothesis. Moreover, some evidences could suggest a putative role of hCNT2 and hCNT3 as transceptors. The interacting proteins identified for hCNT2 suggest a link to energy metabolism. Moreover, the ability of hCNT2 and hCNT3 to transport adenosine links both proteins to purinergic signaling. On the other hand, the broad selectivity transporters hENTs have a crucial role in salvage pathways and purinergic signaling by means of nucleoside pools regulation. In particular, the two new hENT2 isoforms recently described together with hENT2 seem to be key elements controlling nucleoside and nucleotide pools for DNA synthesis. This review focuses on all these NTs functions beyond their mere translocation ability.

摘要

自从人类核苷转运体(hNTs)作为转运系统被其活性鉴定以来,人们已经开展了大量工作以在分子和生理水平上对其进行全面表征。许多努力都致力于确定它们对天然底物和用于治疗多种疾病的核苷类似物的选择性。hNTs属于两个不同的基因家族,分别编码人类浓缩型核苷转运体(hCNTs)和人类平衡型核苷转运体(hENTs)。hCNTs和hENTs是整合膜蛋白,尽管在结构上不相关。这两个家族具有共同特征,如底物选择性和通常的组织定位。这种明显的生物学冗余可能预示着hCNTs和hENTs在细胞生理学中具有一些不同的作用。因此,hENTs可能在维持核苷稳态中起主要作用,而hCNTs可能有助于核苷传感和信号转导。从这个意义上说,将hCNT1归类为转ceptor强化了这一假设。此外,一些证据表明hCNT2和hCNT3可能具有转ceptor的作用。为hCNT2鉴定的相互作用蛋白表明其与能量代谢有关。此外,hCNT2和hCNT3转运腺苷的能力使这两种蛋白都与嘌呤能信号传导相关。另一方面,具有广泛选择性的转运体hENTs通过调节核苷池在补救途径和嘌呤能信号传导中起关键作用。特别是,最近描述的两种新的hENT2同工型与hENT2一起似乎是控制DNA合成的核苷和核苷酸池的关键元件。本综述重点关注所有这些NTs除了其单纯转运能力之外的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b184/5997781/84c8b6ec7726/fphar-09-00606-g001.jpg

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