Synchronization of interconnected networks: the role of connector nodes

In this Letter we identify the general rules that determine the synchronization properties of interconnected networks. We study analytically, numerically and experimentally how the degree of the nodes through which two networks are connected influences the ability of the whole system to synchronize. We show that connecting the high-degree (low-degree) nodes of each network turns out to be the most (least) effective strategy to achieve synchronization. We find the functional relation between synchronizability and size for a given network-of-networks, and report the existence of the optimal connector link weights for the different interconnection strategies. Finally, we perform an electronic experiment with two coupled star networks and conclude that the analytical results are indeed valid in the presence of noise and parameter mismatches.Comment: Accepted for publication in Physical Review Letters. Main text: 5 pages, 4 figures. Supplemental material: 8 pages, 3 figure

Topological Measure Locating the Effective Crossover between Segregation and Integration in a Modular Network

We introduce an easily computable topological measure which locates the effective crossover between segregation and integration in a modular network. Segregation corresponds to the degree of network modularity, while integration is expressed in terms of the algebraic connectivity of an associated hyper-graph. The rigorous treatment of the simplified case of cliques of equal size that are gradually rewired until they become completely merged, allows us to show that this topological crossover can be made to coincide with a dynamical crossover from cluster to global synchronization of a system of coupled phase oscillators. The dynamical crossover is signaled by a peak in the product of the measures of intra-cluster and global synchronization, which we propose as a dynamical measure of complexity. This quantity is much easier to compute than the entropy (of the average frequencies of the oscillators), and displays a behavior which closely mimics that of the dynamical complexity index based on the latter. The proposed toplogical measure simultaneously provides information on the dynamical behavior, sheds light on the interplay between modularity vs total integration and shows how this affects the capability of the network to perform both local and distributed dynamical tasks

Experimental implementation of maximally synchronizable networks

Maximally synchronizable networks (MSNs) are acyclic directed networks that maximize synchronizability. In this paper, we investigate the feasibility of transforming networks of coupled oscillators into their corresponding MSNs. By tuning the weights of any given network so as to reach the lowest possible eigenratio lambdaN/lambda2, the synchronized state is guaranteed to be maintained across the longest possible range of coupling strengths. We check the robustness of the resulting MSNs with an experimental implementation of a network of nonlinear electronic oscillators and study the propagation of the synchronization errors through the network. Importantly, a method to study the effects of topological uncertainties on the synchronizability is proposed and explored both theoretically and experimentally.The authors acknowledge J.L. Echenausía-Monroy, V.P. Vera-Ávila, J. Moreno de León, C. Hapo and P.L. del Barrio for assistance in the laboratory, and the support of MINECO (FIS2012-38949-C03-01 and FIS2013-41057-P). One anonymous referee is acknowledged for having provided valuable advice that has influenced our understanding of the origin of the propagation of the synchronization error, and helped us improve the manuscript in several ways. The authors also acknowledge the computational resources, facilities and assistance provided by the Centro computazionale di RicErca sui Sistemi COmplessi (CRESCO) of the Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA). R.S.E. acknowledges Universidad de Guadalajara, CULagos (Mexico) for financial support (PRO-SNI-2015/228069, PROINPEP/005/2014, UDG-CONACyT/I010/163/2014) and CONACyT (Becas Mixtas MZO2015/290842). D.-U. Hwang acknowledges National Institute for Mathematical Sciences (NIMS) funded by the Ministry of Science, ICT & Future Planning (A21501-3)

Antimicrobial peptides of the Cecropin-family show potent antitumor activity against bladder cancer cells

<p>Abstract</p> <p>Background</p> <p>This study evaluated the cytotoxic and antiproliferative efficacy of two well-characterized members of the Cecropin-family of antimicrobial peptides against bladder tumor cells and benign fibroblasts.</p> <p>Methods</p> <p>The antiproliferative and cytotoxic potential of the Cecropins A and B was quantified by colorimetric WST-1-, BrdU- and LDH-assays in four bladder cancer cell lines as well as in murine and human fibroblast cell lines. IC₅₀values were assessed by logarithmic extrapolation, representing the concentration at which cell viability was reduced by 50%. Scanning electron microscopy (SEM) was performed to visualize the morphological changes induced by Cecropin A and B in bladder tumor cells and fibroblasts.</p> <p>Results</p> <p>Cecropin A and B inhibit bladder cancer cell proliferation and viability in a dose-dependent fashion. The average IC₅₀values of Cecropin A and B against all bladder cancer cell lines ranged between 73.29 μg/ml and 220.05 μg/ml. In contrast, benign fibroblasts were significantly less or not at all susceptible to Cecropin A and B. Both Cecropins induced an increase in LDH release from bladder tumor cells whereas benign fibroblasts were not affected. SEM demonstrated lethal membrane disruption in bladder cancer cells as opposed to fibroblasts.</p> <p>Conclusion</p> <p>Cecropin A and B exert selective cytotoxic and antiproliferative efficacy in bladder cancer cells while sparing targets of benign murine or human fibroblast origin. Both peptides may offer novel therapeutic strategies for the treatment of bladder cancer with limited cytotoxic effects on benign cells.</p