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相似的[DE]XXXL[LI]基序在中华仓鼠卵巢细胞中对葡萄糖转运蛋白8(GLUT8)和葡萄糖转运蛋白12(GLUT12)具有不同的靶向作用。

Similar [DE]XXXL[LI] motifs differentially target GLUT8 and GLUT12 in Chinese hamster ovary cells.

作者信息

Flessner Lauren B, Moley Kelle H

机构信息

Department of Obsetrics and Gynecology, Washington University School of Medicine, 660 South Euclid Ave, St Louis, MO 63110, USA.

出版信息

Traffic. 2009 Mar;10(3):324-33. doi: 10.1111/j.1600-0854.2008.00866.x. Epub 2008 Dec 9.

Abstract

The transport of glucose across cell membranes is mediated by facilitative glucose transporters (GLUTs). The recently identified class III GLUT12 is predominantly expressed in insulin-sensitive tissues such as heart, fat and skeletal muscle. We examined the subcellular localization of GLUT12 in Chinese hamster ovary and human embryonic kidney 293 cells stably expressing murine GLUT12. We have previously shown that another class III GLUT8 contains a [DE]XXXL[LI] motif that directs it to late endosomal/lysosomal compartments. Despite also having this highly conserved motif in its amino terminus, GLUT12 does not colocalize with GLUT8. Rather, GLUT12 resides in the Golgi network and at the plasma membrane (PM). Furthermore, GLUT8 and GLUT12 exhibit dramatic differences in trafficking from the PM. Whereas GLUT8 is internalized following its expression at the cell surface, GLUT12 remains largely associated with the PM. To further explore the trafficking mechanisms, we created mutant constructs to explore the potential role of GLUT12's NH(2)-terminal dileucine motif in regulating its intracellular sorting. We show that both the GPN and the LL residues within the [DE]XXXL[LI] motif influence the cell surface expression of GLUT12 and conclude that the mechanisms governing the intracellular sorting of GLUT12 are distinct from those regulating the sorting of GLUT8.

摘要

葡萄糖跨细胞膜的转运由易化葡萄糖转运体(GLUTs)介导。最近发现的Ⅲ类转运体GLUT12主要在胰岛素敏感组织如心脏、脂肪和骨骼肌中表达。我们检测了稳定表达小鼠GLUT12的中国仓鼠卵巢细胞和人胚肾293细胞中GLUT12的亚细胞定位。我们之前已表明,另一种Ⅲ类转运体GLUT8含有一个[DE]XXXL[LI]基序,该基序将其导向晚期内体/溶酶体区室。尽管GLUT12在其氨基末端也有这个高度保守的基序,但它并不与GLUT8共定位。相反,GLUT12定位于高尔基体网络和质膜(PM)。此外,GLUT8和GLUT12在从质膜的转运方面表现出显著差异。GLUT8在细胞表面表达后会被内化,而GLUT12在很大程度上仍与质膜相关。为了进一步探索转运机制,我们构建了突变体以研究GLUT12的NH(2)-末端双亮氨酸基序在调节其细胞内分选方面的潜在作用。我们发现[DE]XXXL[LI]基序内的GPN和LL残基均影响GLUT12的细胞表面表达,并得出结论,调控GLUT12细胞内分选的机制与调控GLUT8分选的机制不同。

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