Xu X S, Xu T S, Robertson D G, Lambeth J D
Department of Biochemistry, Emory University Medical School, Atlanta, Georgia 30322.
J Biol Chem. 1989 Oct 25;264(30):17674-80.
Pregnenolone synthesis from cholesterol by adrenal mitochondria isolated from ether-stressed rats exhibits a biphasic time course: upon the addition of a reducing substrate (e.g. malate), a rapid phase of pregnenolone formation occurs during the first 5 min, which has been interpreted as the metabolism of a steroidogenic pool of cholesterol, probably in the inner membrane. A slower rate follows, which is interpreted as translocation of cholesterol into the steroidogenic pool. While a 30-min preincubation of mitochondria with cholesterol alone did not affect the extent of the rapid phase, preincubation with GTP plus cholesterol extended the first phase, resulting in an up to 2-fold increase in pregnenolone synthesis by 20-30 min. The apparent Km for GTP was 0.1-0.4 mM, and stimulation was maximal with preincubation times of 10-30 min, depending upon incubation conditions. Exogenous cholesterol was not required to observe a stimulatory effect, indicating that GTP reorganizes the endogenous mitochondrial cholesterol pools. Nevertheless, stimulation was greater when exogenous cholesterol was provided, consistent with enhanced utilization of both endogenous and exogenous cholesterol. Stimulation by GTP was also seen in mitochondria isolated from cycloheximide-injected/ether-stressed rats, although the activity in these preparations was always lower than that in mitochondria from ether-stressed rats. The stimulation was specific for GTP, since many other nucleotides (e.g. ATP, GDP, and ITP) and GTP analogues (guanosine 5'-O-(3-thiotriphosphate and guanosine 5'-(beta,gamma-imino)triphosphate) had no effect. The GTP-activated state was reversible: after GTP hydrolysis by a mitochondrial GTPase, pregnenolone synthesis returned to the basal level. Sonic disruption of mitochondria abolished the stimulatory effect of GTP. These results suggest that GTP enhances pregnenolone synthesis by promoting the movement of cholesterol to the steroidogenic pool, consistent with a recently proposed general role for GTP in some vectorial transport processes (Bourne, H. R. (1988) Cell 53, 669-671).
从经乙醚应激的大鼠分离出的肾上腺线粒体中,由胆固醇合成孕烯醇酮呈现双相时间进程:加入还原底物(如苹果酸)后,最初5分钟内孕烯醇酮形成快速阶段,这被解释为可能在内膜的胆固醇类固醇生成池的代谢。随后速率较慢,被解释为胆固醇转运至类固醇生成池。单独用胆固醇对线粒体进行30分钟预孵育不影响快速阶段的程度,但用GTP加胆固醇预孵育可延长第一阶段,导致20 - 30分钟时孕烯醇酮合成增加高达2倍。GTP的表观Km为0.1 - 0.4 mM,根据孵育条件,预孵育10 - 30分钟时刺激作用最大。观察到刺激作用无需外源性胆固醇,表明GTP可重组内源性线粒体胆固醇池。然而,提供外源性胆固醇时刺激作用更强,这与内源性和外源性胆固醇利用增加一致。在从注射环己酰亚胺/经乙醚应激的大鼠分离出的线粒体中也观察到GTP的刺激作用,尽管这些制剂中的活性总是低于经乙醚应激大鼠的线粒体中的活性。该刺激作用对GTP具有特异性,因为许多其他核苷酸(如ATP、GDP和ITP)以及GTP类似物(鸟苷5'-O-(3-硫代三磷酸)和鸟苷5'-(β,γ-亚氨基)三磷酸)均无作用。GTP激活状态是可逆的:线粒体GTP酶水解GTP后,孕烯醇酮合成恢复到基础水平。线粒体超声破碎消除了GTP的刺激作用。这些结果表明,GTP通过促进胆固醇向类固醇生成池的移动来增强孕烯醇酮合成,这与最近提出的GTP在某些向量运输过程中的一般作用一致(伯恩,H. R.(1988年)《细胞》53卷,669 - 671页)。