Mooney R A, Ebersohl R D, McDonald J M
Eur J Biochem. 1983 Nov 15;136(3):603-8. doi: 10.1111/j.1432-1033.1983.tb07783.x.
Use of a digitonin-permeabilized rat adipocyte preparation overcomes inherent problems which occur when currently used broken cell systems are utilized for studying the regulation of hormone-sensitive lipase. The effect of digitonin on plasma membrane permeability was concentration-dependent being nearly maximum at 20 micrograms/ml as assessed by (a) leakage of 85% cellular lactate dehydrogenase after 30 min, (b) the efflux of 72% preloaded cellular (86Rb) rubidium within 10 min and (c) immediate inhibition of glucose oxidation. Hormone-modulated rates of lipolysis were preserved in this preparation. Following maximal activation of lipolysis in adipocytes with catecholamines, the rate of lipolysis in intact cells and digitonin-treated cells was elevated 26-fold and 20-fold respectively, while the rate in homogenates from these cells was elevated only 2.8-fold. Insulin suppressed catecholamine-dependent activation of lipolysis by at least 90% when subsequently measured in intact cells and digitonin-treated cells. Insulin suppression was only 56% when measured in homogenates. The hormone-sensitive lipase in permeabilized cells, as opposed to intact cells and homogenates, was activated by cyclic AMP to a degree that approached activation by catecholamines. In homogenates, cyclic AMP (1.0 mM) plus ATP (0.25 mM) activated the lipase only 36%, while neither alone had any effect. In digitonin-permeabilized cells, however, exogenous cyclic AMP alone activated lipolysis in a concentration-dependent manner with 1 microM, 30 microM and 1.0 mM cyclic AMP activating lipolysis by 41%, 250% and 1300% respectively. In contrast, lipolysis in intact cells was activated by 0%, 25% and 250% by 1 microM, 30 microM and 1.0 mM cyclic AMP. Also in digitonin-treated preparations, ATP alone activated lipolysis 40%, but ATP plus cyclic AMP activated lipolysis to only 74% of the level due to cyclic AMP alone. These studies indicate that the permeabilized adipocyte preparation is an excellent system for investigating the mechanism of regulation of the hormone-sensitive lipase by permitting manipulation of the intracellular environment while preserving the physiological response of the lipase.
使用洋地黄皂苷通透的大鼠脂肪细胞制剂克服了当前使用破碎细胞系统研究激素敏感性脂肪酶调节时出现的固有问题。洋地黄皂苷对质膜通透性的影响呈浓度依赖性,在20微克/毫升时接近最大值,这通过以下指标评估:(a) 30分钟后85%的细胞乳酸脱氢酶泄漏;(b) 10分钟内72%预先加载的细胞(86Rb)铷外流;(c) 葡萄糖氧化立即受到抑制。在该制剂中保留了激素调节的脂解速率。在用儿茶酚胺使脂肪细胞中的脂解达到最大激活后,完整细胞和洋地黄皂苷处理细胞中的脂解速率分别提高了26倍和20倍,而这些细胞匀浆中的脂解速率仅提高了2.8倍。随后在完整细胞和洋地黄皂苷处理细胞中测量时,胰岛素抑制儿茶酚胺依赖性脂解激活至少90%。在匀浆中测量时,胰岛素抑制率仅为56%。与完整细胞和匀浆相反,通透细胞中的激素敏感性脂肪酶被环磷酸腺苷激活的程度接近儿茶酚胺激活的程度。在匀浆中,1.0毫摩尔/升的环磷酸腺苷加0.25毫摩尔/升的三磷酸腺苷仅激活脂肪酶36%,而单独使用两者均无任何作用。然而在洋地黄皂苷通透的细胞中,单独的外源性环磷酸腺苷以浓度依赖性方式激活脂解,1微摩尔/升、30微摩尔/升和1.0毫摩尔/升的环磷酸腺苷分别激活脂解41%、250%和1300%。相比之下,1微摩尔/升、30微摩尔/升和1.0毫摩尔/升环磷酸腺苷在完整细胞中激活脂解的比例分别为0%、25%和250%。同样在洋地黄皂苷处理的制剂中,单独的三磷酸腺苷激活脂解40%,但三磷酸腺苷加环磷酸腺苷激活脂解的水平仅为单独环磷酸腺苷所致水平的74%。这些研究表明,通透的脂肪细胞制剂是研究激素敏感性脂肪酶调节机制的极佳系统,因为它允许在保持脂肪酶生理反应的同时操纵细胞内环境。