Tennes K A, McKinney J S, Putney J W
Biochem J. 1987 Mar 15;242(3):797-802. doi: 10.1042/bj2420797.
Metabolism of inositol 1,4,5-trisphosphate was investigated in permeabilized guinea-pig hepatocytes. The conversion of [3H]inositol 1,4,5-trisphosphate to a more polar 3H-labelled compound occurred rapidly and was detected as early as 5 s. This material co-eluted from h.p.l.c. with inositol 1,3,4,5 tetrakis[32P]phosphate and is presumably an inositol tetrakisphosphate. A significant increase in the 3H-labelled material co-eluting from h.p.l.c. with inositol 1,3,4-trisphosphate occurred only after a definite lag period. Incubation of permeabilized hepatocytes with inositol 1,3,4,5-tetrakis[32P]phosphate resulted in the formation of 32P-labelled material that co-eluted with inositol 1,3,4-trisphosphate; no inositol 1,4,5-tris[32P]phosphate was produced, suggesting the action of a 5-phosphomonoesterase. The half-time of hydrolysis of inositol 1,3,4,5-tetrakis[32P]phosphate of approx. 1 min was increased to 3 min by 2,3-bisphosphoglyceric acid. Similarly, the rate of production of material tentatively designed as inositol 1,3,4-tris[32P]phosphate from the tetrakisphosphate was reduced by 10 mM-2,3-bisphosphoglyceric acid. In the absence of ATP there was no conversion of [3H]inositol 1,4,5-trisphosphate to [3H]inositol tetrakisphosphate or to [3H]inositol 1,3,4-trisphosphate, which suggests that the 1,3,4 isomer does not result from isomerization of inositol 1,4,5-trisphosphate. The results of this study suggest that the origin of the 1,3,4 isomer of inositol trisphosphate in isolated hepatocytes is inositol 1,3,4,5-tetrakisphosphate and that inositol 1,4,5-trisphosphate is rapidly converted to this tetrakisphosphate. The ability of 2,3-bisphosphoglyceric acid, an inhibitor of 5-phosphomonoesterase of red blood cell membrane, to inhibit the breakdown of the tetrakisphosphate suggests that the enzyme which removes the 5-phosphate from inositol 1,4,5-trisphosphate may also act to convert the tetrakisphosphate to inositol 1,3,4-trisphosphate. It is not known if the role of inositol 1,4,5-trisphosphate kinase is to inactivate inositol 1,4,5-trisphosphate or whether the tetrakisphosphate product may have a messenger function in the cell.
在透化的豚鼠肝细胞中研究了肌醇1,4,5 -三磷酸的代谢。[3H]肌醇1,4,5 -三磷酸向极性更强的3H标记化合物的转化迅速发生,最早在5秒时即可检测到。该物质与肌醇1,3,4,5 -四[32P]磷酸从高效液相色谱中共同洗脱,推测为肌醇四磷酸。只有在一段确定的延迟期后,与肌醇1,3,4 -三磷酸从高效液相色谱中共同洗脱的3H标记物质才会显著增加。用肌醇1,3,4,5 -四[32P]磷酸孵育透化的肝细胞会导致形成与肌醇1,3,4 -三磷酸共同洗脱的32P标记物质;未产生肌醇1,4,5 -三[32P]磷酸,这表明存在5 -磷酸单酯酶的作用。肌醇1,3,4,5 -四[32P]磷酸的水解半衰期约为1分钟,2,3 -二磷酸甘油酸可将其延长至3分钟。同样,10 mM的2,3 -二磷酸甘油酸会降低从四磷酸中初步认定为肌醇1,3,4 -三[32P]磷酸的物质的生成速率。在没有ATP的情况下,[3H]肌醇1,4,5 -三磷酸不会转化为[3H]肌醇四磷酸或[3H]肌醇1,3,4 -三磷酸,这表明1,3,4异构体并非由肌醇1,4,5 -三磷酸异构化产生。本研究结果表明,分离的肝细胞中肌醇三磷酸1,3,4异构体的来源是肌醇1,3,4,5 -四磷酸,且肌醇1,4,5 -三磷酸会迅速转化为这种四磷酸。红细胞膜5 -磷酸单酯酶的抑制剂2,3 -二磷酸甘油酸能够抑制四磷酸的分解,这表明从肌醇1,4,5 -三磷酸去除5 -磷酸的酶可能也会将四磷酸转化为肌醇1,3,4 -三磷酸。目前尚不清楚肌醇1,4,5 -三磷酸激酶的作用是使肌醇1,4,5 -三磷酸失活,还是四磷酸产物在细胞中可能具有信使功能。