Zambrzycka Agata, Kacprzak Maria
Department of Cellular Signaling, Medical Research Center, Polish Academy of Sciences, Pawińskiego 5, PL 02-106 Warsaw, Poland.
Pol J Pharmacol. 2003 Sep-Oct;55(5):911-3.
Polyphosphoinositides synthesized by phosphatidylinositol 4-kinase, EC 2.7.1.67 (PI4K) and phosphatidylinositol 4-phosphate 5-kinase, EC 2.7.1.68 (PIP5K) are involved in cell signaling and cytoskeleton function. In this study, the effect of apolipoprotein E4 (apoE4) and amyloid beta peptide A beta 1-42 on PI4K and PIP5K activity in cortical synaptic plasma membranes from rat brain was investigated. The results indicated that 0.25 microM apoE4 inhibited PI4K and PIP5K by 40% and 30%, respectively, but 25 microM A beta 1-42 decreased exclusively PI4K activity by 20%. Although the mechanism of apoE4 and A beta action is unknown and needs future investigation, this study suggests that free radical-dependent protein oxidation may be involved in alteration of these enzymes.
由磷脂酰肌醇4 -激酶(EC 2.7.1.67,PI4K)和磷脂酰肌醇4 -磷酸5 -激酶(EC 2.7.1.68,PIP5K)合成的多磷酸肌醇参与细胞信号传导和细胞骨架功能。在本研究中,研究了载脂蛋白E4(apoE4)和β淀粉样肽Aβ1 - 42对大鼠大脑皮质突触质膜中PI4K和PIP5K活性的影响。结果表明,0.25微摩尔的apoE4分别抑制PI4K和PIP5K活性40%和30%,但25微摩尔的Aβ1 - 42仅使PI4K活性降低20%。尽管apoE4和Aβ作用的机制尚不清楚,需要进一步研究,但本研究表明自由基依赖性蛋白质氧化可能参与了这些酶的改变。