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1.
Artif Life ; 29(1): 66-93, 2023 01 02.
Article in English | MEDLINE | ID: mdl-36173656

ABSTRACT

While interest in artificial neural networks (ANNs) has been renewed by the ubiquitous use of deep learning to solve high-dimensional problems, we are still far from general artificial intelligence. In this article, we address the problem of emergent cognitive capabilities and, more crucially, of their detection, by relying on co-evolving creatures with mutable morphology and neural structure. The former is implemented via both static and mobile structures whose shapes are controlled by cubic splines. The latter uses ESHyperNEAT to discover not only appropriate combinations of connections and weights but also to extrapolate hidden neuron distribution. The creatures integrate low-level perceptions (touch/pain proprioceptors, retina-based vision, frequency-based hearing) to inform their actions. By discovering a functional mapping between individual neurons and specific stimuli, we extract a high-level module-based abstraction of a creature's brain. This drastically simplifies the discovery of relationships between naturally occurring events and their neural implementation. Applying this methodology to creatures resulting from solitary and tag-team co-evolution showed remarkable dynamics such as range-finding and structured communication. Such discovery was made possible by the abstraction provided by the modular ANN which allowed groups of neurons to be viewed as functionally enclosed entities.


Subject(s)
Artificial Intelligence , Magnetic Resonance Imaging , Neural Networks, Computer , Neurons/physiology
2.
Cell Cycle ; 18(8): 795-808, 2019 04.
Article in English | MEDLINE | ID: mdl-30870080

ABSTRACT

Modeling and in silico simulations are of major conceptual and applicative interest in studying the cell cycle and proliferation in eukaryotic cells. In this paper, we present a cell cycle checkpoint-oriented simulator that uses agent-based simulation modeling to reproduce the dynamics of a cancer cell population in exponential growth. Our in silico simulations were successfully validated by experimental in vitro supporting data obtained with HCT116 colon cancer cells. We demonstrated that this model can simulate cell confluence and the associated elongation of the G1 phase. Using nocodazole to synchronize cancer cells at mitosis, we confirmed the model predictivity and provided evidence of an additional and unexpected effect of nocodazole on the overall cell cycle progression. We anticipate that this cell cycle simulator will be a potential source of new insights and research perspectives.


Subject(s)
Colonic Neoplasms/metabolism , Computer Simulation , G1 Phase Cell Cycle Checkpoints/drug effects , Nocodazole/pharmacology , Cell Proliferation/drug effects , Colonic Neoplasms/pathology , Eukaryotic Cells/metabolism , HCT116 Cells , Humans , Kinetics , Mitosis/drug effects , Tumor Microenvironment
3.
Biosystems ; 94(1-2): 95-101, 2008.
Article in English | MEDLINE | ID: mdl-18616980

ABSTRACT

Cell pattern generation has a fundamental role in both artificial and natural development. This paper presents results from a model in which a genetic algorithm (GA) was used to evolve an artificial regulatory network (ARN) to produce predefined 2D cell patterns through the selective activation and inhibition of genes. The ARN used in this work is an extension of a model previously used to create simple geometrical patterns. The GA worked by evolving the gene regulatory network that was used to control cell reproduction, which took place in a testbed based on cellular automata (CA). After the final chromosomes were produced, a single cell in the middle of the CA lattice was allowed to replicate controlled by the ARN found by the GA, until the desired cell pattern was formed. The model was applied to the problem of generating a French flag pattern.


Subject(s)
Algorithms , Cell Growth Processes , Computational Biology/methods , Gene Regulatory Networks , Models, Genetic
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