1,972 research outputs found
The impact of cellular characteristics on the evolution of shape homeostasis
The importance of individual cells in a developing multicellular organism is
well known but precisely how the individual cellular characteristics of those
cells collectively drive the emergence of robust, homeostatic structures is
less well understood. For example cell communication via a diffusible factor
allows for information to travel across large distances within the population,
and cell polarisation makes it possible to form structures with a particular
orientation, but how do these processes interact to produce a more robust and
regulated structure? In this study we investigate the ability of cells with
different cellular characteristics to grow and maintain homeostatic structures.
We do this in the context of an individual-based model where cell behaviour is
driven by an intra-cellular network that determines the cell phenotype. More
precisely, we investigated evolution with 96 different permutations of our
model, where cell motility, cell death, long-range growth factor (LGF),
short-range growth factor (SGF) and cell polarisation were either present or
absent. The results show that LGF has the largest positive impact on the
fitness of the evolved solutions. SGF and polarisation also contribute, but all
other capabilities essentially increase the search space, effectively making it
more difficult to achieve a solution. By perturbing the evolved solutions, we
found that they are highly robust to both mutations and wounding. In addition,
we observed that by evolving solutions in more unstable environments they
produce structures that were more robust and adaptive. In conclusion, our
results suggest that robust collective behaviour is most likely to evolve when
cells are endowed with long range communication, cell polarisation, and
selection pressure from an unstable environment
Decoding the regulatory network of early blood development from single-cell gene expression measurements.
Reconstruction of the molecular pathways controlling organ development has been hampered by a lack of methods to resolve embryonic progenitor cells. Here we describe a strategy to address this problem that combines gene expression profiling of large numbers of single cells with data analysis based on diffusion maps for dimensionality reduction and network synthesis from state transition graphs. Applying the approach to hematopoietic development in the mouse embryo, we map the progression of mesoderm toward blood using single-cell gene expression analysis of 3,934 cells with blood-forming potential captured at four time points between E7.0 and E8.5. Transitions between individual cellular states are then used as input to develop a single-cell network synthesis toolkit to generate a computationally executable transcriptional regulatory network model of blood development. Several model predictions concerning the roles of Sox and Hox factors are validated experimentally. Our results demonstrate that single-cell analysis of a developing organ coupled with computational approaches can reveal the transcriptional programs that underpin organogenesis.We thank J. Downing (St. Jude Children's Research Hospital, Memphis, TN, USA) for the Runx1-ires-GFP mouse. Research in the authors' laboratory is supported by the Medical Research Council, Biotechnology and Biological Sciences Research Council, Leukaemia and Lymphoma Research, the Leukemia and Lymphoma Society, Microsoft Research and core support grants by the Wellcome Trust to the Cambridge Institute for Medical Research and Wellcome Trust - MRC Cambridge Stem Cell Institute. V.M. is supported by a Medical Research Council Studentship and Centenary Award and S.W. by a Microsoft Research PhD Scholarship.This is the accepted manuscript for a paper published in Nature Biotechnology 33, 269–276 (2015) doi:10.1038/nbt.315
Applications of Biological Cell Models in Robotics
In this paper I present some of the most representative biological models
applied to robotics. In particular, this work represents a survey of some
models inspired, or making use of concepts, by gene regulatory networks (GRNs):
these networks describe the complex interactions that affect gene expression
and, consequently, cell behaviour
Morphogenesis by coupled regulatory networks: Reliable control of positional information and proportion regulation
Based on a non-equilibrium mechanism for spatial pattern formation we study
how position information can be controlled by locally coupled discrete
dynamical networks, similar to gene regulation networks of cells in a
developing multicellular organism. As an example we study the developmental
problems of domain formation and proportion regulation in the presence of
noise, as well as in the presence of cell flow. We find that networks that
solve this task exhibit a hierarchical structure of information processing and
are of similar complexity as developmental circuits of living cells. Proportion
regulation is scalable with system size and leads to sharp, precisely localized
boundaries of gene expression domains, even for large numbers of cells. A
detailed analysis of noise-induced dynamics, using a mean-field approximation,
shows that noise in gene expression states stabilizes (rather than disrupts)
the spatial pattern in the presence of cell movements, both for stationary as
well as growing systems. Finally, we discuss how this mechanism could be
realized in the highly dynamic environment of growing tissues in multi-cellular
organisms.Comment: Journal of Theoretical Biology, in pres
Experimental observation of chimera and cluster states in a minimal globally coupled network
A "chimera state" is a dynamical pattern that occurs in a network of coupled
identical oscillators when the symmetry of the oscillator population is broken
into synchronous and asynchronous parts. We report the experimental observation
of chimera and cluster states in a network of four globally coupled chaotic
opto-electronic oscillators. This is the minimal network that can support
chimera states, and our study provides new insight into the fundamental
mechanisms underlying their formation. We use a unified approach to determine
the stability of all the observed partially synchronous patterns, highlighting
the close relationship between chimera and cluster states as belonging to the
broader phenomenon of partial synchronization. Our approach is general in terms
of network size and connectivity. We also find that chimera states often appear
in regions of multistability between global, cluster, and desynchronized
states
Data based identification and prediction of nonlinear and complex dynamical systems
We thank Dr. R. Yang (formerly at ASU), Dr. R.-Q. Su (formerly at ASU), and Mr. Zhesi Shen for their contributions to a number of original papers on which this Review is partly based. This work was supported by ARO under Grant No. W911NF-14-1-0504. W.-X. Wang was also supported by NSFC under Grants No. 61573064 and No. 61074116, as well as by the Fundamental Research Funds for the Central Universities, Beijing Nova Programme.Peer reviewedPostprin
Evolving Gene Regulatory Networks with Mobile DNA Mechanisms
This paper uses a recently presented abstract, tuneable Boolean regulatory
network model extended to consider aspects of mobile DNA, such as transposons.
The significant role of mobile DNA in the evolution of natural systems is
becoming increasingly clear. This paper shows how dynamically controlling
network node connectivity and function via transposon-inspired mechanisms can
be selected for in computational intelligence tasks to give improved
performance. The designs of dynamical networks intended for implementation
within the slime mould Physarum polycephalum and for the distributed control of
a smart surface are considered.Comment: 7 pages, 8 figures. arXiv admin note: substantial text overlap with
arXiv:1303.722
- …