Devaskar S, Zahm D S, Holtzclaw L, Chundu K, Wadzinski B E
Department of Pediatrics, St. Louis University School of Medicine, Missouri.
Endocrinology. 1991 Sep;129(3):1530-40. doi: 10.1210/endo-129-3-1530.
We examined the immunohistochemical localization of Glut 1 in sections of developing rat brain [gestational (G) days 18 and 20, postnatal (P) days 1, 10, 21, and greater than 40; term = approximately G21] and characterized the abundance of Glut 1 in isolated brain microvessels by Western blot analysis. Further quantitation of total glucose transporters by [125I]3-iodo-4-azido-phenethyl-amido-7-O-succinyldeacetyl-forskoli n photoaffinity labeling was performed. Glut 1 was prominently distributed in G18 and P1 brain vascular endothelial cells, with comparatively little immunoreactivity observed in brain parenchyma. Conversely, at P10, Glut 1 was prominent in brain parenchyma (undifferentiated cells) and less evident in the vascular endothelium. However, at P21, a resurgence of Glut 1 in vascular endothelial cells was observed, as was a sustained presence in parenchymal cells. On P greater than 40, a distribution in vascular endothelial cells and, to a minor extent, in parenchymal perivascular stellate cells was noted. Microvessel preparation Glut 1 (approximately 55-60 kDa) and [125I] 3-iodo-4-azido-phenethyl-amido-7-O-succinyldeacetyl-forskolin photoaffinity-labeled glucose transporters gradually increased from G18 through P10 to P greater than 40. This developmental increase in Glut 1 was also seen in whole homogenates (approximately 45-47 kDa), but not in crude brain membranes. Thus, isolated microvascular preparations indicated that Glut 1 levels constantly increased with maturation, but direct visualization of brain sections revealed that the localization in different cellular compartments changed with development. These alterations in cellular localization of glucose transporters, appear to occur in concert with the changing glucose metabolic needs of the brain, which, during the various stages of development, exhibits constantly changing phases of cellular growth and proliferation.
我们检测了发育中大鼠脑切片(妊娠第18和20天、出生后第1、10、21天及大于40天;足月约为妊娠21天)中葡萄糖转运蛋白1(Glut 1)的免疫组化定位,并通过蛋白质印迹分析对分离的脑微血管中Glut 1的丰度进行了表征。通过[125I]3 - 碘 - 4 - 叠氮基苯乙酰胺 - 7 - O - 琥珀酰去乙酰佛司可林光亲和标记法进一步对总葡萄糖转运体进行了定量分析。Glut 1在妊娠18天和出生后第1天的脑血管内皮细胞中分布显著,在脑实质中观察到的免疫反应性相对较少。相反,在出生后第10天,Glut 1在脑实质(未分化细胞)中显著,而在血管内皮中不太明显。然而,在出生后第21天,观察到Glut 1在血管内皮细胞中再次出现,并且在实质细胞中持续存在。在出生后大于40天,注意到其分布于血管内皮细胞,在较小程度上也分布于实质血管周围的星状细胞。微血管制备物中Glut 1(约55 - 60 kDa)和[125I]3 - 碘 - 4 - 叠氮基苯乙酰胺 - 7 - O - 琥珀酰去乙酰佛司可林光亲和标记的葡萄糖转运体从妊娠18天到出生后第10天再到出生后大于40天逐渐增加。这种Glut 1的发育性增加在全匀浆(约45 - 47 kDa)中也可见,但在粗制脑膜中未见。因此,分离的微血管制备物表明Glut 1水平随成熟而持续增加,但脑切片的直接观察显示其在不同细胞区室中的定位随发育而变化。葡萄糖转运体细胞定位的这些改变似乎与大脑不断变化的葡萄糖代谢需求协同发生,大脑在发育的各个阶段表现出细胞生长和增殖不断变化的阶段。