Ito Laboratory and Nagao Laboratory, RIKEN Brain Science Institute, Saitama 351-0198, Japan.
Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3198-203. doi: 10.1073/pnas.0915020107. Epub 2010 Jan 28.
In this study, we show the crucial roles of lipid signaling in long-term depression (LTD), that is, synaptic plasticity prevailing in cerebellar Purkinje cells. In mouse brain slices, we found that cPLA(2)alpha knockout blocked LTD induction, which was rescued by replenishing arachidonic acid (AA) or prostaglandin (PG) D(2) or E(2). Moreover, cyclooxygenase (COX)-2 inhibitors block LTD, which is rescued by supplementing PGD(2)/E(2). The blockade or rescue occurs when these reagents are applied within a time window of 5-15 min following the onset of LTD-inducing stimulation. Furthermore, PGD(2)/E(2) facilitates the chemical induction of LTD by a PKC activator but is unable to rescue the LTD blocked by a PKC inhibitor. We conclude that PGD(2)/E(2) mediates LTD jointly with PKC, and suggest possible pathways for their interaction. Finally, we demonstrate in awake mice that cPLA(2)alpha deficiency or COX-2 inhibition attenuates short-term adaptation of optokinetic eye movements, supporting the view that LTD underlies motor learning.
在这项研究中,我们展示了脂质信号在长时程抑制(LTD)中的关键作用,即小脑浦肯野细胞中占主导地位的突触可塑性。在小鼠脑切片中,我们发现 cPLA2α 敲除阻止了 LTD 的诱导,而补充花生四烯酸(AA)或前列腺素(PG)D2 或 E2 则可以挽救。此外,环氧化酶(COX)-2 抑制剂阻断 LTD,而补充 PGD2/E2 则可以挽救。这些试剂在 LTD 诱导刺激开始后的 5-15 分钟时间窗口内应用时会发生阻断或挽救。此外,PGD2/E2 通过 PKC 激活剂促进 LTD 的化学诱导,但不能挽救 PKC 抑制剂阻断的 LTD。我们得出结论,PGD2/E2 与 PKC 共同介导 LTD,并提出了它们相互作用的可能途径。最后,我们在清醒的小鼠中证明,cPLA2α 缺失或 COX-2 抑制减弱了光运动眼球运动的短期适应,支持 LTD 是运动学习的基础这一观点。