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在动脉平滑肌中,膜相关二酰基甘油激酶活性可被去甲肾上腺素增强,但不能被血管紧张素II增强。

Membrane-associated diacylglycerol kinase activity is increased by noradrenaline, but not by angiotensin II, in arterial smooth muscle.

作者信息

Ohanian J, Heagerty A M

机构信息

Department of Medicine, University Hospital of South Manchester, U.K.

出版信息

Biochem J. 1994 May 15;300 ( Pt 1)(Pt 1):51-6. doi: 10.1042/bj3000051.

Abstract

In rat small arteries, noradrenaline stimulates the sustained production of arachidonoyl-phosphatidic acid, whereas there is only a slight and transient increase with angiotensin II [Ohanian, Ollerenshaw, Collins and Heagerty (1990) J. Biol. Chem. 265, 8921-8928]. Diacylglycerol kinase (DGK) is the enzyme responsible for generating phosphatidic acid from 1,2-diacylglycerol (DAG). To investigate whether agonists influence DGK activity, we have studied this enzyme in both particulate and soluble fractions prepared from rat small arteries. Soluble DGK activity was inhibited by octyl glucoside. Therefore a deoxycholate assay was used for this fraction, whereas an octyl glucoside mixed-micelle assay was used to examine particulate fractions. Particulate DGK selectively phosphorylated long-chain DAG at a rate 2.5-3-fold higher than that for the synthetic substrate dioctanoylglycerol. In contrast, the substrate preference of the soluble isoenzyme(s) was: dioctanoylglycerol > arachidonoyl-DAG= dioleoylglycerol. Stimulation of intact arteries with noradrenaline (15 microM) increased membrane-associated DGK activity 3-fold, transiently. Angiotensin II (100 nM) stimulation did not alter the DGK activity of this fraction. The activity of the soluble DGK was increased by both agonists, but only transiently. These results demonstrate that rat small arteries contain a membrane-associated DGK which metabolizes arachidonoyl-containing substrate. Also, the activity of this enzyme is regulated differentially by vasoconstrictor hormones. It is concluded that modulation of DGK activity may represent one point at which agonists using the same signal-transduction pathway may tailor the cellular response.

摘要

在大鼠小动脉中,去甲肾上腺素刺激花生四烯酰磷脂酸的持续产生,而血管紧张素II仅引起轻微且短暂的增加[奥哈尼安、奥勒伦肖、柯林斯和希格蒂(1990年)《生物化学杂志》265卷,8921 - 8928页]。二酰基甘油激酶(DGK)是负责从1,2 - 二酰基甘油(DAG)生成磷脂酸的酶。为了研究激动剂是否影响DGK活性,我们在从大鼠小动脉制备的微粒体和可溶性部分中研究了这种酶。可溶性DGK活性受到辛基葡糖苷的抑制。因此,该部分采用脱氧胆酸盐测定法,而微粒体部分则采用辛基葡糖苷混合胶束测定法。微粒体DGK选择性地磷酸化长链DAG,其速率比合成底物二辛酰甘油高2.5 - 3倍。相比之下,可溶性同工酶的底物偏好为:二辛酰甘油>花生四烯酰 - DAG =二油酰甘油。用去甲肾上腺素(15微摩尔)刺激完整动脉会使膜相关DGK活性瞬时增加3倍。血管紧张素II(100纳摩尔)刺激并未改变该部分的DGK活性。两种激动剂均使可溶性DGK的活性增加,但只是瞬时增加。这些结果表明,大鼠小动脉含有一种膜相关的DGK,它能代谢含花生四烯酸的底物。此外,这种酶的活性受到血管收缩激素的不同调节。得出的结论是,DGK活性的调节可能是使用相同信号转导途径的激动剂调整细胞反应的一个点。

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