Glucose transporters in pancreatic islets

被引:82
作者
Berger, Constantin [1 ]
Zdzieblo, Daniela [1 ,2 ]
机构
[1] Univ Hosp Wurzburg, Tissue Engn Regenerat Med, Rontgenring 11, D-97070 Wurzburg, Germany
[2] Fraunhofer Inst Silicate Res ISC, Translat Ctr Regenerat Therapies, Neunerplatz 2, D-97082 Wurzburg, Germany
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2020年 / 472卷 / 09期
关键词
Glucose transport; Pancreatic islet; beta-Cell; alpha-Cell; GLUTs; SGLTs; FANCONI-BICKEL-SYNDROME; INSULIN GENE-TRANSCRIPTION; UNRESPONSIVE BETA-CELLS; SENSITIVE K+ CHANNELS; HIGH-FAT DIET; GLUT2; EXPRESSION; ALPHA-CELLS; GLUCAGON-SECRETION; SUGAR TRANSPORTER; SGLT2; INHIBITORS;
D O I
10.1007/s00424-020-02383-4
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The fine-tuning of glucose uptake mechanisms is rendered by various glucose transporters with distinct transport characteristics. In the pancreatic islet, facilitative diffusion glucose transporters (GLUTs), and sodium-glucose cotransporters (SGLTs) contribute to glucose uptake and represent important components in the glucose-stimulated hormone release from endocrine cells, therefore playing a crucial role in blood glucose homeostasis. This review summarizes the current knowledge about cell type-specific expression profiles as well as proven and putative functions of distinct GLUT and SGLT family members in the human and rodent pancreatic islet and further discusses their possible involvement in onset and progression of diabetes mellitus. In context of GLUTs, we focus on GLUT2, characterizing the main glucose transporter in insulin-secreting beta-cells in rodents. In addition, we discuss recent data proposing that other GLUT family members, namely GLUT1 and GLUT3, render this task in humans. Finally, we summarize latest information about SGLT1 and SGLT2 as representatives of the SGLT family that have been reported to be expressed predominantly in the alpha-cell population with a suggested functional role in the regulation of glucagon release.
引用
收藏
页码:1249 / 1272
页数:24
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