Kerr J S, Reicherter J, Fisher A B
Am J Physiol. 1982 Jul;243(1):C14-9. doi: 10.1152/ajpcell.1982.243.1.C14.
Uptake of 2-deoxy-D-glucose (DG) was investigated with rat granular pneumocytes isolated in primary culture. Cells attached to flasks were incubated in Minimal Essential Medium usually containing 5 mM DG in place of glucose. Uptake of DG increased progressively with time of incubation and approached a plateau value of 35-40 mumol/10(6) cells at 60 min. Uptake increased as a function of external DG concentration with half-maximal uptake at approximately 2.0 mM DG. DG uptake was inhibited by the presence of glucose, alpha-methylglucoside, phlorizin, ouabain, or sodium-free medium. After 60 min incubation, approximately 20% of total intracellular DG was in the free form, and the calculated mean intracellular concentration of free DG (n = 4) was approximately twice the external concentration. Phosphatase activity was indicated by increase in free DG and efflux from cells after removal of external DG. In comparison with pneumocytes, uptake of DG by alveolar macrophages showed different kinetics, and intracellular free DG did not exceed the extracellular concentration. These findings indicate that type II cells take up DG by a sodium-dependent, carrier-mediated transport process that results in accumulation of free sugar against a concentration gradient.
用原代培养分离的大鼠颗粒性肺细胞研究了2-脱氧-D-葡萄糖(DG)的摄取情况。贴壁在培养瓶上的细胞在通常含有5 mM DG以代替葡萄糖的最低必需培养基中孵育。DG的摄取随着孵育时间的延长而逐渐增加,在60分钟时接近35 - 40 μmol/10⁶个细胞的平台值。摄取量随着细胞外DG浓度的增加而增加,在约2.0 mM DG时摄取量达到最大值的一半。葡萄糖、α-甲基葡萄糖苷、根皮苷、哇巴因或无钠培养基的存在会抑制DG的摄取。孵育60分钟后,细胞内总DG中约20%呈游离形式,计算得出的游离DG平均细胞内浓度(n = 4)约为细胞外浓度的两倍。去除细胞外DG后,游离DG的增加和从细胞中的流出表明存在磷酸酶活性。与肺细胞相比,肺泡巨噬细胞对DG的摄取表现出不同的动力学,并且细胞内游离DG不超过细胞外浓度。这些发现表明II型细胞通过钠依赖性、载体介导的转运过程摄取DG,该过程导致游离糖逆浓度梯度积累。