Germinario R J, Colby-Germinario S P, Cammalleri C, Wainberg M A
Lady Davis Institute for Medical Research, SMBD Jewish General Hospital, 3755 Cote St Catherine Road, Montreal, Quebec, Canada.
J Endocrinol. 2003 Sep;178(3):449-56. doi: 10.1677/joe.0.1780449.
The objective of this study was to investigate the long-term effects of anti-retroviral protease inhibitors (PIs) on 2-deoxy-d -glucose (2-DG) transport in L6 cells in vitro. Exposure of L6 cells to saquinavir, ritonavir, indinavir and amprenavir resulted in significant increases in 2-DG transport using PI concentrations of 1-10 microM with continual exposure to PI. After removal of the PI for up to 48 h, 2-DG transport increases did not change and remained at pre-reversal levels. These changes in 2-DG transport were not related to stress-induced sugar transport or to apoptosis. The examination of glucose transporter (GLUT) 1, 3 or 4 translocation with subcellular fractionation indicated that insulin (i.e. 67 nM) could induce the translocation of all the GLUTs to the plasma membrane. Also, ritonavir (10 microM), which leads to a 2-fold increase in 2-DG transport, demonstrated increased GLUT (i.e. 1, 3 or 4) presence in the plasma membrane fraction, in the presence or absence of insulin. This increased 2-DG transport involved transporter presence in plasma membrane preparations and did not affect the ability of insulin to stimulate 2-DG transport with continual PI exposure. The mechanism(s) involved indicates ready reversibility of PI effects on transporters. The mechanism(s) why reversibility of PI-induced 2-DG transport was similar plus or minus PI was not apparent.
本研究的目的是调查抗逆转录病毒蛋白酶抑制剂(PIs)对体外培养的L6细胞中2-脱氧-D-葡萄糖(2-DG)转运的长期影响。将L6细胞暴露于沙奎那韦、利托那韦、茚地那韦和安普那韦中,使用1-10 microM的PI浓度并持续暴露于PI,会导致2-DG转运显著增加。去除PI长达48小时后,2-DG转运增加并未改变,仍保持在去除PI前的水平。2-DG转运的这些变化与应激诱导的糖转运或细胞凋亡无关。通过亚细胞分级分离对葡萄糖转运蛋白(GLUT)1、3或4易位的检测表明,胰岛素(即67 nM)可诱导所有GLUT易位至质膜。此外,导致2-DG转运增加2倍的利托那韦(10 microM),在有或无胰岛素存在的情况下,均显示质膜组分中GLUT(即1、3或4)的存在增加。这种2-DG转运增加涉及质膜制剂中转运蛋白的存在,并且在持续暴露于PI的情况下不影响胰岛素刺激2-DG转运的能力。所涉及的机制表明PI对转运蛋白的作用具有可逆性。PI诱导的2-DG转运无论有无PI其可逆性相似的原因尚不明确。