Department of Physiology and Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
Am J Physiol Endocrinol Metab. 2010 Feb;298(2):E141-5. doi: 10.1152/ajpendo.00712.2009. Epub 2009 Dec 15.
The ability to take up and metabolize glucose at the cellular level is a property shared by the vast majority of existing organisms. Most mammalian cells import glucose by a process of facilitative diffusion mediated by members of the Glut (SLC2A) family of membrane transport proteins. Fourteen Glut proteins are expressed in the human and they include transporters for substrates other than glucose, including fructose, myoinositol, and urate. The primary physiological substrates for at least half of the 14 Glut proteins are either uncertain or unknown. The well-established glucose transporter isoforms, Gluts 1-4, are known to have distinct regulatory and/or kinetic properties that reflect their specific roles in cellular and whole body glucose homeostasis. Separate review articles on many of the Glut proteins have recently appeared in this journal. Here, we provide a very brief summary of the known properties of the 14 Glut proteins and suggest some avenues of future investigation in this area.
在细胞水平摄取和代谢葡萄糖的能力是绝大多数现有生物共有的特性。大多数哺乳动物细胞通过易化扩散过程来摄取葡萄糖,该过程由 Glut(SLC2A)家族的膜转运蛋白成员介导。在人类中表达了 14 种 Glut 蛋白,它们包括除葡萄糖以外的底物的转运蛋白,包括果糖、肌醇和尿酸。至少一半的 14 种 Glut 蛋白的主要生理底物尚不确定或未知。已确定的葡萄糖转运蛋白同工型 Gluts 1-4 具有独特的调节和/或动力学特性,反映了它们在细胞和全身葡萄糖稳态中的特定作用。本刊最近发表了许多 Glut 蛋白的专题评论文章。在这里,我们对这 14 种 Glut 蛋白的已知特性进行了简要总结,并提出了该领域未来研究的一些途径。