Augert G, Blackmore P F, Exton J H
Howard Hughes Medical Institute, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
J Biol Chem. 1989 Feb 15;264(5):2574-80.
The hormonal regulation of phosphoinositide levels in isolated hepatocytes was studied using chemical means. Extracted inositol phospholipids were adsorbed to neomycin-coated glass beads and then eluted and quantitated by charring after separation by thin layer chromatography on silica gel. The amounts (in nanograms/mg wet weight) of phosphatidylinositol 4,5-bisphosphate (PIP2), phosphatidylinositol 4-phosphate (PIP), and phosphatidylinositol (PI) were 20 +/- 1, 16 +/- 1, and 1790 +/- 140, respectively). Incubation of the cells with 100 nM vasopressin decreased the value for PIP2 to 10 +/- 0.2 at 15 s, 12 +/- 1.5 at 1 min, and 14 +/- 2.1 at 5 and 30 min. In contrast, the hormone increased 1,2-diacylglycerol plus phosphatidate by over 200 ng/mg wet weight at 5 min under similar conditions (Bocckino, S. B., Blackmore, P. F., Wilson, P. B., and Exton, J. H. (1987) J. Biol. Chem. 262, 15309-15315). PIP2 was also significantly decreased at 15 s by angiotensin II (100 nM), ATP (100 microM), and epinephrine (1 microM). In contrast, PIP was not significantly changed, and PI was significantly decreased (by approximately 15%) at later times (15 and 30 min). The changes in phosphoinositide mass were well correlated with changes in labeled phosphoinositides in hepatocytes previously incubated with [3H]inositol for 90 min. The amounts of inositol phospholipids in liver plasma membranes (in micrograms/mg protein) were 2.1 +/- 0.2 for PIP2, 0.24 +/- 0.03 for PIP, and 23 +/- 4 for PI. Comparison of these values with those for whole cells suggests that PIP2 is enriched in the plasma membrane, whereas PIP is present elsewhere in the cell. The fatty acid composition of whole cell PIP2 showed significant differences from that of PI. The percentages of palmitic, stearic, linoleic, and arachidonic acids were, respectively, 14, 41, 10, and 25 for PIP2 and 10, 34, 7, and 37 for PI. Vasopressin treatment for 15 s did not alter the fatty acid composition of PIP2. The corresponding fatty acid percentages for liver plasma membranes were 13, 41, 11, and 21 for PIP2 and 8, 34, 0, and 40 for PI. The fatty acid composition of PIP in whole cells and plasma membranes resembled that of PIP2.(ABSTRACT TRUNCATED AT 400 WORDS)
采用化学方法研究了离体肝细胞中磷酸肌醇水平的激素调节。提取的肌醇磷脂吸附到新霉素包被的玻璃珠上,然后洗脱,经硅胶薄层层析分离后通过炭化进行定量。磷脂酰肌醇4,5-二磷酸(PIP2)、磷脂酰肌醇4-磷酸(PIP)和磷脂酰肌醇(PI)的含量(以纳克/毫克湿重计)分别为20±1、16±1和1790±140。用100 nM血管加压素孵育细胞15秒时,PIP2的值降至10±0.2,1分钟时为12±1.5,5分钟和30分钟时为14±2.1。相反,在类似条件下,5分钟时该激素使1,2-二酰基甘油加磷脂酸增加超过200纳克/毫克湿重(博基诺,S.B.,布莱克莫尔,P.F.,威尔逊,P.B.,和埃克斯顿,J.H.(1987年)《生物化学杂志》262,15309 - 15315)。血管紧张素II(100 nM)、ATP(100 microM)和肾上腺素(1 microM)在15秒时也使PIP2显著降低。相反,PIP没有显著变化,PI在稍后时间(15分钟和30分钟)显著降低(约15%)。磷酸肌醇质量的变化与先前用[3H]肌醇孵育90分钟的肝细胞中标记的磷酸肌醇的变化密切相关。肝细胞膜中肌醇磷脂的含量(以微克/毫克蛋白质计),PIP2为2.1±0.2,PIP为0.24±0.03,PI为23±4。将这些值与全细胞的值进行比较表明,PIP2在质膜中富集,而PIP存在于细胞的其他部位。全细胞PIP2的脂肪酸组成与PI有显著差异。棕榈酸、硬脂酸、亚油酸和花生四烯酸的百分比,PIP2分别为14%、41%、10%和25%,PI分别为10%、34%、7%和37%。用血管加压素处理15秒未改变PIP2的脂肪酸组成。肝细胞膜中PIP2相应的脂肪酸百分比为棕榈酸13%、硬脂酸41%、亚油酸