Rincón M, Chen Q, Boss W F
Department of Botany, North Carolina State University, Raleigh, North Carolina 27695-7612.
Plant Physiol. 1989 Jan;89(1):126-32. doi: 10.1104/pp.89.1.126.
We have shown previously that inositol-1,4,5-trisphosphate (IP(3)) stimulates an efflux of (45)Ca(2+) from fusogenic carrot protoplasts (M Rincón, WF Boss [1987] Plant Physiol 83: 395-398). In light of these results, we suggested that IP(3) might serve as a second messenger for the mobilization of intracellular Ca(2+) in higher plant cells. To determine whether or not IP(3) and other inositol phosphates were present in the carrot cells, the cells were labeled with myo-[2-(3)H]inositol for 18 hours and extracted with ice-cold 10% trichloroacetic acid. The inositol metabolites were separated by anion exchange chromatography and by paper electrophoresis. We found that [(3)H]inositol metabolites coeluted with inositol bisphosphate (IP(2)) and IP(3) when separated by anion exchange chromatography. However, we could not detect IP(2) or IP(3) when the inositol metabolites were analyzed by paper electrophoresis even though the polyphosphoinositides, which are the source of IP(2) and IP(3), were present in these cells. Thus, [(3)H] inositol metabolites other than IP(2) and IP(3) had coeluted on the anion exchange columns. The data indicate that either IP(3) is rapidly metabolized or that it is not present at a detectable level in the carrot cells.
我们之前已经表明,肌醇 - 1,4,5 - 三磷酸(IP(3))可刺激融合性胡萝卜原生质体中(45)Ca(2+)的外流(M·林孔,WF·博斯[1987]《植物生理学》83: 395 - 398)。鉴于这些结果,我们推测IP(3)可能作为高等植物细胞中动员细胞内Ca(2+)的第二信使。为了确定胡萝卜细胞中是否存在IP(3)和其他肌醇磷酸,细胞用肌醇 - [2-(3)H]肌醇标记18小时,并用冰冷的10%三氯乙酸提取。肌醇代谢产物通过阴离子交换色谱法和纸电泳法进行分离。我们发现,通过阴离子交换色谱法分离时,[(3)H]肌醇代谢产物与肌醇二磷酸(IP(2))和IP(3)共洗脱。然而,当通过纸电泳分析肌醇代谢产物时,我们无法检测到IP(2)或IP(3),尽管作为IP(2)和IP(3)来源的多磷酸肌醇存在于这些细胞中。因此,除IP(2)和IP(3)之外的[(3)H]肌醇代谢产物在阴离子交换柱上共洗脱。数据表明,要么IP(3)迅速代谢,要么它在胡萝卜细胞中不存在可检测的水平。