76 research outputs found
The Evolution of Robust Development and Homeostasis in Artificial Organisms
During embryogenesis, multicellular animals are shaped via cell proliferation, cell rearrangement, and apoptosis. At the end of development, tissue architecture is then maintained through balanced rates of cell proliferation and loss. Here, we take an in silico approach to look for generic systems features of morphogenesis in multicellular animals that arise as a consequence of the evolution of development. Using artificial evolution, we evolved cellular automata-based digital organisms that have distinct embryonic and homeostatic phases of development. Although these evolved organisms use a variety of strategies to maintain their form over time, organisms of different types were all found to rapidly recover from environmental damage in the form of wounds. This regenerative response was most robust in an organism with a stratified tissue-like architecture. An evolutionary analysis revealed that evolution itself contributed to the ability of this organism to maintain its form in the face of genetic and environmental perturbation, confirming the results of previous studies. In addition, the exceptional robustness of this organism to surface injury was found to result from an upward flux of cells, driven in part by cell divisions with a stable niche at the tissue base. Given the general nature of the model, our results lead us to suggest that many of the robust systems properties observed in real organisms, including scar-free wound-healing in well-protected embryos and the layered tissue architecture of regenerating epithelial tissues, may be by-products of the evolution of morphogenesis, rather than the direct result of selection
Lithium chloride therapy fails to improve motor function in a transgenic mouse model of Machado-Joseph disease
The accumulation of misfolded proteins in neurons, leading to the formation of cytoplasmic and nuclear aggregates, is a common theme in age-related neurodegenerative diseases, possibly due to disturbances of the proteostasis and insufficient activity of cellular protein clearance pathways. Lithium is a well-known autophagy inducer that exerts neuroprotective effects in different conditions and has been proposed as a promising therapeutic agent for several neurodegenerative diseases. We tested the efficacy of chronic lithium 10.4 mg/kg) treatment in a transgenic mouse model of Machado-Joseph disease, an inherited neurodegenerative disease, caused by an expansion of a polyglutamine tract within the protein ataxin-3. A battery of behavioral tests was used to assess disease progression. In spite of activating autophagy, as suggested by the increased levels of Beclin-1, Atg7, and LC3II, and a reduction in the p62 protein levels, lithium administration showed no overall beneficial effects in this model concerning motor performance, showing a positive impact only in the reduction of tremors at 24 weeks of age. Our results do not support lithiumchronic treatment as a promising strategy for the treatment of Machado-Joseph disease (MJD).FCT -Fundação para a Ciência e a Tecnologia(SFRH/BD/51059/2010
A1-L12 interfacial free energies from data on coarsening in five binary Ni alloys, informed by thermodynamic phase diagram assessments
Nanoparticle enhanced solders for high temperature environments
Nanoparticle enhanced solders have been reported to have superior creep and reliability properties compared to simple alloyed materials. The nanoparticles, typically added at 1-2 wt% concentrations into the solder serve to harden the solder, stabilize the microstructure and improve reliability in high temperature environments. The nanoparticles may be added to the solder before production of solder particles, or added as a separate ingredient of the solder paste. This paper explores the latter approach. For this investigation, nanoparticles composed of a silica dielectric core and Au metallic shell were used, and the efficacy of different synthesis routes compared. In particular, it was found that Poly diallyldimethyl ammonium Chloride (PDADMAC), served as a better linker molecule than 3-Aminopropyltrimethoxysilane (APTMS) for attaching the shell to the core. However, even with solder wettable shells, it was found that the majority of the particles were expelled from the SAC solder during reflow in air, and the causes were examined with the aid of Computational Fluid Dynamics to model the reflow process. © 2007 IEEE
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