Verjans B, Erneux C, Raspe E, Dumont J E
Institute of Interdisciplinary Research (IRIBHN), School of Medicine, Free University of Brussels (ULB), Belgium.
Eur J Biochem. 1991 Feb 26;196(1):43-9. doi: 10.1111/j.1432-1033.1991.tb15783.x.
The action of carbachol on the generation of inositol trisphosphate and tetrakisphosphate isomers was investigated in dog-thyroid primary cultured cells radiolabelled with [3H]inositol. The separation of the inositol phosphate isomers was performed by reverse-phase high pressure liquid chromatography. The structure of inositol phosphates co-eluting with inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] and inositol 1,3,4,5-tetrakisphosphate [Ins(1,3,4,5)P4] standards was determined by enzymatic degradation using a purified Ins(1,4,5)P3/Ins(1,3,4,5)P4 5-phosphatase. The data indicate that Ins(1,3,4,5)P4 was the only [3H]inositol phosphate which co-eluted with a [32P]Ins(1,3,4,5)P4 standard, whereas 80% of the [3H]InsP3 co-eluting with an Ins(1,4,5)P3 standard was actually this isomer. In the presence of Li+, carbachol led to rapid increases in [3H]Ins(1,4,5)P4. The level of Ins(1,4,5)P3 reached a peak at 200% of the control after 5-10 s of stimulation and fell to a plateau that remained slightly elevated for 2 min. The level of Ins(1,3,4,5)P4 reached its maximum at 20s. The level of inositol 1,3,4-trisphosphate [Ins(1,3,4)P3] increased continuously for 2 min after the addition of carbachol. Inositol-phosphate generation was also investigated under different pharmacological conditions. Li+ largely increased the level of Ins(1,3,4)P3 but had no effect on Ins(1,4,5)P3 and Ins(1,3,4,5)P4. Forskolin, which stimulates dog-thyroid adenylate cyclase and cyclic-AMP accumulation, had no effect on the generation of inositol phosphates. The absence of extracellular Ca2+ largely decreased the level of Ins(1,3,4,5)P4 as expected considering the Ca2(+)-calmodulin sensitivity of the Ins(1,4,5)P3 3-kinase. Staurosporine, an inhibitor of protein kinase C, increased the levels of Ins(1,4,5)P3, Ins(1,3,4,5)P4 and Ins(1,3,4)P3. This supports a negative feedback control of diacyglycerol on Ins(1,4,5)P3 generation.
在以[3H]肌醇进行放射性标记的犬甲状腺原代培养细胞中,研究了卡巴胆碱对肌醇三磷酸和四磷酸异构体生成的作用。肌醇磷酸异构体的分离通过反相高压液相色谱法进行。与肌醇1,4,5 - 三磷酸[Ins(1,4,5)P3]和肌醇1,3,4,5 - 四磷酸[Ins(1,3,4,5)P4]标准品共洗脱的肌醇磷酸的结构,通过使用纯化的Ins(1,4,5)P3/Ins(1,3,4,5)P4 5 - 磷酸酶进行酶促降解来确定。数据表明,Ins(1,3,4,5)P4是唯一与[32P]Ins(1,3,4,5)P4标准品共洗脱的[3H]肌醇磷酸,而与Ins(1,4,5)P3标准品共洗脱的[3H]InsP3中80%实际上是该异构体。在Li +存在的情况下,卡巴胆碱导致[3H]Ins(1,4,5)P4迅速增加。刺激5 - 10秒后,Ins(1,4,5)P3水平达到对照的200%的峰值,然后降至一个平台期,该平台期在2分钟内仍略有升高。Ins(1,3,4,5)P4水平在20秒时达到最大值。加入卡巴胆碱后,肌醇1,3,4 - 三磷酸[Ins(1,3,4)P3]水平持续增加2分钟。还在不同药理条件下研究了肌醇磷酸的生成。Li +大大增加了Ins(1,3,4)P3的水平,但对Ins(1,4,5)P3和Ins(1,3,4,5)P4没有影响。刺激犬甲状腺腺苷酸环化酶并促进环磷酸腺苷积累的福斯高林,对肌醇磷酸的生成没有影响。如考虑到Ins(1,4,5)P3 3 - 激酶对Ca2(+) - 钙调蛋白的敏感性,细胞外Ca2 +的缺失如预期的那样大大降低了Ins(1,3,4,5)P4的水平。蛋白激酶C抑制剂星形孢菌素增加了Ins(1,4,5)P3、Ins(1,3,4,5)P4和Ins(1,3,4)P3的水平。这支持了二酰基甘油对Ins(1,4,5)P3生成的负反馈控制。