植入前发育中的葡萄糖转运蛋白。

M Pantaleon, P L Kaye
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引用次数: 119

摘要

胚胎在压实之前不能利用葡萄糖作为燃料一直是一个有很多推测的领域。有人认为,葡萄糖转运体过程的限制是造成这种情况的主要原因。最近鉴定的GLUT3是负责压实后母体葡萄糖摄取的转运体,可能提供了这个谜题中缺失的一环。此外,它的表达与胚胎葡萄糖利用的开始一致表明,GLUT3可能参与了胚胎代谢优先权的决定。基于GLUT3和GLUT1两种促进性葡萄糖转运蛋白的功能,提出了一个囊胚摄取葡萄糖的模型,该模型可以适应生长因子对胚胎过程的调节,并且与GLUT蛋白的生化特性和胚胎的生理特征相一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glucose transporters in preimplantation development.

The inability of the embryo to utilize glucose as a fuel before compaction has been an area of much speculation. It is suggested that limitations in glucose transporter processes are the prime reasons for this. The recent identification of GLUT3 as the transporter responsible for the uptake of maternal glucose after compaction may provide the missing link in this puzzle. Furthermore, the coincidence of its expression with the onset of embryonic glucose utilization suggests that GLUT3 may be involved in the determination of metabolic priorities of the embryo. A model for the uptake of glucose by the blastocyst based on the function of two facilitative glucose transporters, GLUT3 and GLUT1, is proposed which can accommodate growth factor regulation of embryonic processes and is consistent with both the well established biochemical characteristics of GLUT proteins and the physiology of the embryo.

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