Bashan N, Potashnik R, Hagay Y, Moses S W
Pediatric Research Laboratory, Soroka Medical Center, Beer Sheva, Israel.
J Inherit Metab Dis. 1987;10(3):234-41. doi: 10.1007/BF01800068.
A study of 2-deoxyglucose transport into polymorphonuclear leukocytes (PMN) was performed in three patients with glycogen storage disease (GSD) type Ib. The rate of 2-deoxyglucose transport into GSD Ib PMN was 30% of that of cells of normal controls. In GSD Ib lymphocytes, transport was normal. Km for 2-deoxyglucose in the PMN of one patient was within the normal range. The reduced transport was not due to the elevation in Km for 2-deoxyglucose nor to the decreased rate of phosphorylation of 2-deoxyglucose. The striking limitation of glucose transport across the cell membrane may account for the impairment of leukocyte function which is characteristic of GSD Ib.
对三名患有Ib型糖原贮积病(GSD)的患者进行了关于2-脱氧葡萄糖转运至多形核白细胞(PMN)的研究。2-脱氧葡萄糖转运至GSD Ib型PMN的速率为正常对照细胞的30%。在GSD Ib型淋巴细胞中,转运正常。一名患者的PMN中2-脱氧葡萄糖的Km在正常范围内。转运减少并非由于2-脱氧葡萄糖的Km升高,也不是由于2-脱氧葡萄糖磷酸化速率降低。葡萄糖跨细胞膜转运的显著受限可能解释了GSD Ib所特有的白细胞功能损害。