1,386 research outputs found
Ratio control in a cascade model of cell differentiation
We propose a kind of reaction-diffusion equations for cell differentiation,
which exhibits the Turing instability. If the diffusivity of some variables is
set to be infinity, we get coupled competitive reaction-diffusion equations
with a global feedback term. The size ratio of each cell type is controlled by
a system parameter in the model. Finally, we extend the model to a cascade
model of cell differentiation. A hierarchical spatial structure appears as a
result of the cell differentiation. The size ratio of each cell type is also
controlled by the system parameter.Comment: 13 pages, 7 figure
Curvature Dependent Diffusion Flow on Surface with Thickness
Particle diffusion in a two dimensional curved surface embedded in is
considered. In addition to the usual diffusion flow, we find a new flow with an
explicit curvature dependence. New diffusion equation is obtained in
(thickness of surface) expansion. As an example, the surface of elliptic
cylinder is considered, and curvature dependent diffusion coefficient is
calculated.Comment: 8 pages, 8 figures, Late
Turing's model for biological pattern formation and the robustness problem
One of the fundamental questions in developmental biology is how the vast range of pattern and structure we observe in nature emerges from an almost uniformly homogeneous fertilized egg. In particular, the mechanisms by which biological systems maintain robustness, despite being subject to numerous sources of noise, are shrouded in mystery. Postulating plausible theoretical models of biological heterogeneity is not only difficult, but it is also further complicated by the problem of generating robustness, i.e. once we can generate a pattern, how do we ensure that this pattern is consistently reproducible in the face of perturbations to the domain, reaction time scale, boundary conditions and so forth. In this paper, not only do we review the basic properties of Turing's theory, we highlight the successes and pitfalls of using it as a model for biological systems, and discuss emerging developments in the area
Morphogen Transport in Epithelia
We present a general theoretical framework to discuss mechanisms of morphogen
transport and gradient formation in a cell layer. Trafficking events on the
cellular scale lead to transport on larger scales. We discuss in particular the
case of transcytosis where morphogens undergo repeated rounds of
internalization into cells and recycling. Based on a description on the
cellular scale, we derive effective nonlinear transport equations in one and
two dimensions which are valid on larger scales. We derive analytic expressions
for the concentration dependence of the effective diffusion coefficient and the
effective degradation rate. We discuss the effects of a directional bias on
morphogen transport and those of the coupling of the morphogen and receptor
kinetics. Furthermore, we discuss general properties of cellular transport
processes such as the robustness of gradients and relate our results to recent
experiments on the morphogen Decapentaplegic (Dpp) that acts in the fruit fly
Drosophila
Modelling cell motility and chemotaxis with evolving surface finite elements
We present a mathematical and a computational framework for the modelling of cell motility. The cell membrane is represented by an evolving surface, with the movement of the cell determined by the interaction of various forces that act normal to the surface. We consider external forces such as those that may arise owing to inhomogeneities in the medium and a pressure that constrains the enclosed volume, as well as internal forces that arise from the reaction of the cells' surface to stretching and bending. We also consider a protrusive force associated with a reaction-diffusion system (RDS) posed on the cell membrane, with cell polarization modelled by this surface RDS. The computational method is based on an evolving surface finite-element method. The general method can account for the large deformations that arise in cell motility and allows the simulation of cell migration in three dimensions. We illustrate applications of the proposed modelling framework and numerical method by reporting on numerical simulations of a model for eukaryotic chemotaxis and a model for the persistent movement of keratocytes in two and three space dimensions. Movies of the simulated cells can be obtained from http://homepages.warwick.ac.uk/maskae/CV_Warwick/Chemotaxis.html
Mode transitions in a model reaction-diffusion system driven by domain growth and noise
Pattern formation in many biological systems takes place during growth of the underlying domain. We study a specific example of a reaction–diffusion (Turing) model in which peak splitting, driven by domain growth, generates a sequence of patterns. We have previously shown that the pattern sequences which are presented when the domain growth rate is sufficiently rapid exhibit a mode-doubling phenomenon. Such pattern sequences afford reliable selection of certain final patterns, thus addressing the robustness problem inherent of the Turing mechanism. At slower domain growth rates this regular mode doubling breaks down in the presence of small perturbations to the dynamics. In this paper we examine the breaking down of the mode doubling sequence and consider the implications of this behaviour in increasing the range of reliably selectable final patterns
Noise-induced inhibitory suppression of malfunction neural oscillators
Motivated by the aim to find new medical strategies to suppress undesirable
neural synchronization we study the control of oscillations in a system of
inhibitory coupled noisy oscillators. Using dynamical properties of inhibition,
we find regimes when the malfunction oscillations can be suppressed but the
information signal of a certain frequency can be transmitted through the
system. The mechanism of this phenomenon is a resonant interplay of noise and
the transmission signal provided by certain value of inhibitory coupling.
Analyzing a system of three or four oscillators representing neural clusters,
we show that this suppression can be effectively controlled by coupling and
noise amplitudes.Comment: 10 pages, 14 figure
The influence of alfalfa-switchgrass intercropping on microbial community structure and function
The use of nitrogen fertilizer on bioenergy crops such as switchgrass results in increased costs, nitrogen leaching and emissions of N2O, a potent greenhouse gas. Intercropping with nitrogen-fixing alfalfa has been proposed as an environmentally sustainable alternative, but the effects of synthetic fertilizer versus intercropping on soil microbial community functionality remain uncharacterized. We analysed 24 metagenomes from the upper soil layer of agricultural fields from Prosser, WA over two growing seasons and representing three agricultural practices: unfertilized switchgrass (control), fertilized switchgrass and switchgrass intercropped with alfalfa. The synthetic fertilization and intercropping did not result in major shifts of microbial community taxonomic and functional composition compared with the control plots, but a few significant changes were noted. Most notably, mycorrhizal fungi, ammonia-oxidizing archaea and bacteria increased in abundance with intercropping and fertilization. However, only betaproteobacterial ammonia-oxidizing bacteria abundance in fertilized plots significantly correlated to N2O emission and companion qPCR data. Collectively, a short period of intercropping elicits minor but significant changes in the soil microbial community toward nitrogen preservation and that intercropping may be a viable alternative to synthetic fertilization
Converting genetic network oscillations into somite spatial pattern
In most vertebrate species, the body axis is generated by the formation of
repeated transient structures called somites. This spatial periodicity in
somitogenesis has been related to the temporally sustained oscillations in
certain mRNAs and their associated gene products in the cells forming the
presomatic mesoderm. The mechanism underlying these oscillations have been
identified as due to the delays involved in the synthesis of mRNA and
translation into protein molecules [J. Lewis, Current Biol. {\bf 13}, 1398
(2003)]. In addition, in the zebrafish embryo intercellular Notch signalling
couples these oscillators and a longitudinal positional information signal in
the form of an Fgf8 gradient exists that could be used to transform these
coupled temporal oscillations into the observed spatial periodicity of somites.
Here we consider a simple model based on this known biology and study its
consequences for somitogenesis. Comparison is made with the known properties of
somite formation in the zebrafish embryo . We also study the effects of
localized Fgf8 perturbations on somite patterning.Comment: 7 pages, 7 figure
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