Aging decreases phosphatidylinositol-4,5-bisphosphate level but has no effect on activities of phosphoinositide kinases.

Polish journal of pharmacology Pub Date : 2004-09-01
A Zambrzycka
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Abstract

Phosphoinositides play an important role in cell signaling and cytoskeleton function. In this study, we investigate the effect of brain aging on phosphatidylinositol-4-monophosphate (PI(4)P) and phosphatidylinositol-4,5-bisphosphate (PI(4,5)P(2)) synthesis by PI 4-kinase (PI4K) and PI(4)P 5-kinase (PIP5K) in cortical synaptic plasma membranes in the presence of endogenous and exogenous substrates and gamma-[(32)P]ATP. Our data demonstrated that aging decreases PI(4,5)P(2) formation by 40% in the presence of endogenous substrate, but had no effect on PI4K and PIP5K activities. One can hypothesize that aging decreases PI(4,5)P(2) level probably by enhancement of polyphosphoinositides degradation. Alteration of PI(4,5)P(2) concentration may disturb cellular signaling and cytoskeleton dynamics.

衰老降低了磷脂酰肌醇-4,5-二磷酸水平,但对磷脂肌醇激酶的活性没有影响。
磷酸肌苷在细胞信号传导和细胞骨架功能中起重要作用。在这项研究中,我们研究了在内源性和外源性底物和γ -[(32)P]ATP存在的情况下,脑老化对皮质突触质膜中PI4 -激酶(PI4K)和PI(4) p5 -激酶(PIP5K)合成磷脂酰肌醇-4-单磷酸(PI(4)P)和磷脂酰肌醇-4,5-二磷酸(PI(4,5)P(2))的影响。我们的数据表明,在内源底物存在的情况下,衰老使PI(4,5)P(2)的形成减少了40%,但对PI4K和PIP5K活性没有影响。我们可以假设衰老降低PI(4,5)P(2)水平可能是通过增强多磷酸肌苷的降解。PI(4,5)P(2)浓度的改变可能扰乱细胞信号传导和细胞骨架动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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