Vannucci S J, Rutherford T, Wilkie M B, Simpson I A, Lauder J M
Department of Pediatrics and Neuroscience and Anatomy, Hershey Medical Center, Penn State University College of Medicine, 17033, USA.
Dev Neurosci. 2000;22(4):274-82. doi: 10.1159/000017451.
The GLUT4 glucose transporter is primarily expressed in skeletal muscle, heart and adipose tissue, where its expression is postnatal, coincident with the acquisition of insulin-regulated glucose transport. In muscle, contraction also regulates GLUT4 activity in the postnatal animal. Here we demonstrate that GLUT4 is expressed in the developing mouse embryo with specific tissue and spatiotemporal patterns. From embryonic day 9 (E9; E1 = day of copulation plug) to postnatal day 70 (P70), mice were analyzed for GLUT4 mRNA and protein expression by in situ hybridization, immunohistochemistry and immunoblot. Specificity was confirmed with sense riboprobe hybridization and peptide competition, respectively. At E9, GLUT4 was detected in the cranial neural folds in the outer (mantle) layer of the neuroepithelium. At E10, expression was present throughout the developing heart and was prominent in the endocardial cushions through E12. At E10-12, GLUT4 was also prominent in craniofacial mesenchyme. GLUT4 expression in cartilage and bone was evident at E12 and was maintained throughout early postnatal life. GLUT4 was apparent throughout embryonic development in the ventricular epithelium, choroid plexus and in the developing cerebellum. At birth, cardiac expression was reduced and GLUT4 was most evident in cartilage, bone and specific brain regions. In the latter, GLUT4 expression was most evident in the cerebellum, specifically in the external granular layer through P7 and in the internal granular layer thereafter. Maximal GLUT4 protein levels in the cerebellum were measured between P14 and P21 and were reduced in the adult brain. These findings suggest that GLUT4-mediated glucose transport may play important roles during development of the brain and nonneuronal tissues in the mouse embryo.
葡萄糖转运蛋白4(GLUT4)主要在骨骼肌、心脏和脂肪组织中表达,其表达在出生后出现,与胰岛素调节的葡萄糖转运的获得同时发生。在肌肉中,收缩也调节出生后动物体内GLUT4的活性。在此,我们证明GLUT4在发育中的小鼠胚胎中以特定的组织和时空模式表达。从胚胎第9天(E9;E1 = 交配栓出现日)到出生后第70天(P70),通过原位杂交、免疫组织化学和免疫印迹分析小鼠的GLUT4 mRNA和蛋白表达。分别用正义核糖探针杂交和肽竞争法确认了特异性。在E9时,在神经上皮外层(套层)的颅神经褶中检测到GLUT4。在E10时,整个发育中的心脏都有表达,并且在E12之前心内膜垫中表达突出。在E10 - 12时,GLUT4在颅面间充质中也很突出。GLUT4在软骨和骨中的表达在E12时明显,并在出生后早期一直保持。在整个胚胎发育过程中,GLUT4在心室上皮、脉络丛和发育中的小脑中都很明显。出生时,心脏中的表达减少,GLUT4在软骨、骨和特定脑区中最为明显。在后者中,GLUT4表达在小脑中最为明显,具体而言,在P7之前在外部颗粒层中最明显,之后在内部颗粒层中最明显。小脑中GLUT4蛋白水平在P14和P21之间达到最高,在成年大脑中降低。这些发现表明,GLUT4介导的葡萄糖转运可能在小鼠胚胎大脑和非神经组织的发育过程中发挥重要作用。