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13th International Conference on Membrane Computing - MTA Sztaki

13th International Conference on Membrane Computing - MTA Sztaki

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Maintenance of chr<strong>on</strong>obiological informati<strong>on</strong> by P system mediated assembly<br />

of c<strong>on</strong>trol units for oscillatory waveforms and frequency<br />

Fig. 11. Hierarchical scheme of unidirecti<strong>on</strong>ally coupled neur<strong>on</strong>al core oscillators organised<br />

in four layers. Individual oscillati<strong>on</strong>s synchr<strong>on</strong>ise by passing through these<br />

layers. See text for detailed explanati<strong>on</strong>.<br />

stream layers synchr<strong>on</strong>ise their oscillati<strong>on</strong> via unidirecti<strong>on</strong>al molecular coupling<br />

in which the oscillatory outputs of superior layers directly affect oscillati<strong>on</strong>s in<br />

adjacent subsequent layers. Neur<strong>on</strong>s residing in the deepest layer release their<br />

widely synchr<strong>on</strong>ised oscillatory signals to peripheral oscillators in other parts of<br />

the organism. Figure 11 illustrates a small network composed of 14 core oscillators<br />

called n[1] up to n[14] organised within four layers.<br />

We are going to c<strong>on</strong>duct two experimental studies: In a first scenario, we wish<br />

to c<strong>on</strong>sider a pre-synchr<strong>on</strong>ised network with a single neur<strong>on</strong> in the master-clock<br />

layer, see part A of Figure 11. This neur<strong>on</strong> propagates its oscillatory rhythm to<br />

all downstream neur<strong>on</strong>s causing a slight signal delay from layer to layer. After<br />

a short transient phase, all 12 neur<strong>on</strong>s incorporated in this scenario oscillate<br />

synchr<strong>on</strong>ously. Although sufficient so far, a single master clock makes the system<br />

error-pr<strong>on</strong>e and fragile, especially if the master-clock oscillati<strong>on</strong> deviates from<br />

its expected behaviour which can easily happen al<strong>on</strong>g with cell ageing. In this<br />

case, an incorrect or insufficient oscillatory signal runs through all layers without<br />

any correcti<strong>on</strong> or c<strong>on</strong>trol. Additi<strong>on</strong>al master-clock neur<strong>on</strong>s with full c<strong>on</strong>nectivity<br />

to downstream layers can help to stabilise the functi<strong>on</strong> of the whole network.<br />

Our sec<strong>on</strong>d scenario depicted in part B reflects this aspect. Here, we add a<br />

master clock neur<strong>on</strong> and a sec<strong>on</strong>d-layer neur<strong>on</strong> completing the network of 14<br />

neur<strong>on</strong>s. Temporal signal offsets (so-called phase differences) am<strong>on</strong>g individual<br />

master-clock oscillati<strong>on</strong>s are diminished while passing the downstream layers.<br />

Finally, a robust “average” oscillatory signal derived from all master clocks is<br />

released as global output. Our simulati<strong>on</strong> shows that initial phase differences<br />

within the master-clock layer can be reduced up to ≈ 2.6-fold by running through<br />

three subsequent layers, widely independent of the coupling strength. Antiphasic<br />

master-clock oscillati<strong>on</strong>s (half-periodic offset, phase difference 180 ◦ ) turn out to<br />

be resistent against synchr<strong>on</strong>isati<strong>on</strong> by passing the layers almost unaffected.<br />

239

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