Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 305-701, Republic of Korea.
J Cell Sci. 2010 Feb 15;123(Pt 4):537-43. doi: 10.1242/jcs.060061. Epub 2010 Jan 26.
Biological oscillations are found ubiquitously in cells and are widely variable, with periods varying from milliseconds to months, and scales involving subcellular components to large groups of organisms. Interestingly, independent oscillators from different cells often show synchronization that is not the consequence of an external regulator. What is the underlying design principle of such synchronized oscillations, and can modeling show that the complex consequences arise from simple molecular or other interactions between oscillators? When biological oscillators are coupled with each other, we found that synchronization is induced when they are connected together through a positive feedback loop. Increasing the coupling strength of two independent oscillators shows a threshold beyond which synchronization occurs within a few cycles, and a second threshold where oscillation stops. The positive feedback loop can be composed of either double-positive (PP) or double-negative (NN) interactions between a node of each of the two oscillating networks. The different coupling structures have contrasting characteristics. In particular, PP coupling is advantageous with respect to stability of period and amplitude, when local oscillators are coupled with a short time delay, whereas NN coupling is advantageous for a long time delay. In addition, PP coupling results in more robust synchronized oscillations with respect to amplitude excursions but not period, with applied noise disturbances compared to NN coupling. However, PP coupling can induce a large fluctuation in the amplitude and period of the resulting synchronized oscillation depending on the coupling strength, whereas NN coupling ensures almost constant amplitude and period irrespective of the coupling strength. Intriguingly, we have also observed that artificial evolution of random digital oscillator circuits also follows this design principle. We conclude that a different coupling strategy might have been selected according to different evolutionary requirements.
生物振荡器在细胞中无处不在且广泛存在,其周期从毫秒到数月不等,规模从亚细胞成分到生物体的大群体不等。有趣的是,来自不同细胞的独立振荡器通常表现出同步,而这种同步不是外部调节剂的结果。这种同步振荡的潜在设计原则是什么,模型能否表明复杂的结果是由振荡器之间简单的分子或其他相互作用产生的?当生物振荡器彼此耦合时,我们发现当它们通过正反馈回路连接在一起时会产生同步。增加两个独立振荡器之间的耦合强度会显示出一个阈值,超过该阈值,在几个周期内就会发生同步,超过第二个阈值则会停止振荡。正反馈回路可以由两个振荡网络中每个节点之间的双正(PP)或双负(NN)相互作用组成。不同的耦合结构具有不同的特点。特别是,当局部振荡器以短的时间延迟耦合时,PP 耦合在周期和振幅的稳定性方面具有优势,而 NN 耦合在长的时间延迟方面具有优势。此外,与 NN 耦合相比,PP 耦合在受到噪声干扰时会产生更稳健的同步振荡,其幅度和相位的稳定性更高。然而,PP 耦合会根据耦合强度导致同步振荡的幅度和周期产生较大波动,而 NN 耦合则可以确保无论耦合强度如何,幅度和周期几乎保持不变。有趣的是,我们还观察到随机数字振荡器电路的人工进化也遵循这一设计原则。我们得出结论,根据不同的进化需求,可能选择了不同的耦合策略。