1,079 research outputs found
Phase coexistence and relaxation of the spherical frustrated Blume-Emery-Griffiths model with attractive particles coupling
We study the equilibrium and dynamical properties of a spherical version of
the frustrated Blume-Emery-Griffiths model at mean field level for attractive
particle-particle coupling (K>0). Beyond a second order transition line from a
paramagnetic to a (replica symmetric) spin glass phase, the density-temperature
phase diagram is characterized by a tricritical point from which,
interestingly, a first order transition line starts with coexistence of the two
phases. In the Langevin dynamics the paramagnetic/spin glass discontinuous
transition line is found to be dependent on the initial density; close to this
line, on the paramagnetic side, the correlation-response plot displays
interrupted aging.Comment: to be published on Europhysics Letter
Glass glass transition and new dynamical singularity points in an analytically solvable p-spin glass like model
We introduce and analytically study a generalized p-spin glass like model
that captures some of the main features of attractive glasses, recently found
by Mode Coupling investigations, such as a glass/glass transition line and
dynamical singularity points characterized by a logarithmic time dependence of
the relaxation. The model also displays features not predicted by the Mode
Coupling scenario that could further describe the attractive glasses behavior,
such as aging effects with new dynamical singularity points ruled by
logarithmic laws or the presence of a glass spinodal line
Small fragments sodium sulfated hyaluronate, more than hyaluronic acid, reduces LPS-induced cytokine/chemokine levels in HaCaT cells
Hyaluronic acid (HA) is a linear non-sulphated glycosaminoglycan, used in dermatology as a
biomaterial for bioengineering purposes, temporary dermal filler, stimulation of wound healing
as well as drug vehicle in topical formulations. In addition to the well-characterized
structural properties, extensive research on HA has revealed a range of vastly immunemodulatory
effects, dependent on its size. In this in vitro study we investigated the ability of
HA-S3, a small fragment HA (MW, molecular weight: 68 kDa) with degree of sulphatation
of 3 and of HA fraction (MW:210 kDa) to reduce the bacterial induced inflammatory response
in spontaneous immortalized keratinocytes. To this purpose, HaCaT cells were treated for
24 hours with 25 µg/ml of E. Coli derived bacterial lipopolysaccharide (LPS) in absence or
presence of small fragment HA-S3 or HA. Cell viability was thereafter assessed using trypan
blue stain and interleukin (IL)-8, IL-1β and tumor necrosis factor alpha (TNF-α) concentrations
were determined in cell supernatants by single enzyme-linked immunoadsorbent assay
(ELISA). Our results showed that cell viability was not affected either by HA-S3 or HA which
in turn were able to reduce LPS-induced mortality. HA and especially HA-S3 were able to
significantly reduce LPS-induced pro-inflammatory cytokines. Our observation might suggest
new perspectives in the development of HA-S3 containing topical products able to modulate
cutaneous inflammatory response
Spin-Glass Model for Inverse Freezing
We analyze the Blume-Emery-Griffiths model with disordered magnetic
interaction displaying the inverse freezing phenomenon. The behaviour of this
spin-1 model in crystal field is studied throughout the phase diagram and the
transition and spinodal lines for the model are computed using the Full Replica
Symmetry Breaking Ansatz that always yelds a thermodynamically stable phase. We
compare the results both with the quenched disordered model with Ising spins on
lattice gas - where no reentrance takes place - and with the model with
generalized spin variables recently introduced by Schupper and Shnerb [Phys.
Rev. Lett. 93, 037202 (2004)]. The simplest version of all these models, known
as Ghatak-Sherrington model, turns out to hold all the general features
characterizing an inverse transition to an amorphous phase, including the right
thermodynamic behavior.Comment: 6 pages, 4 figures, to appear in the Proceeding for the X
International Workshop on Disordered Systems (2006), Molveno, Ital
Multiscale Bone Remodelling with Spatial P Systems
Many biological phenomena are inherently multiscale, i.e. they are
characterized by interactions involving different spatial and temporal scales
simultaneously. Though several approaches have been proposed to provide
"multilayer" models, only Complex Automata, derived from Cellular Automata,
naturally embed spatial information and realize multiscaling with
well-established inter-scale integration schemas. Spatial P systems, a variant
of P systems in which a more geometric concept of space has been added, have
several characteristics in common with Cellular Automata. We propose such a
formalism as a basis to rephrase the Complex Automata multiscaling approach
and, in this perspective, provide a 2-scale Spatial P system describing bone
remodelling. The proposed model not only results to be highly faithful and
expressive in a multiscale scenario, but also highlights the need of a deep and
formal expressiveness study involving Complex Automata, Spatial P systems and
other promising multiscale approaches, such as our shape-based one already
resulted to be highly faithful.Comment: In Proceedings MeCBIC 2010, arXiv:1011.005
Dynamics and thermodynamics of the spherical frustrated Blume-Emery-Griffiths model
We introduce a spherical version of the frustrated Blume-Emery-Griffiths
model and solve exactly the statics and the Langevin dynamics for zero
particle-particle coupling (K=0). In this case the model exhibits an
equilibrium transition from a disordered to a spin glass phase which is always
continuous for nonzero temperature. The same phase diagram results from the
study of the dynamics. Furthermore, we notice the existence of a nonequilibrium
time regime in a region of the disordered phase, characterized by aging as
occurs in the spin glass phase. Due to a finite equilibration time, the system
displays in this region the pattern of interrupted aging.Comment: 19 pages, 8 figure
Brain organoids: Filling the need for a human model of neurological disorder
Neurological disorders are among the leading causes of death worldwide, accounting for almost all onsets of dementia in the elderly, and are known to negatively affect motor ability, mental and cognitive performance, as well as overall wellbeing and happiness. Currently, most neurological disorders go untreated due to a lack of viable treatment options. The reason for this lack of options is s poor understanding of the disorders, primarily due to research models that do not translate well into the human in vivo system. Current models for researching neurological disorders, neurodevelopment, and drug interactions in the central nervous system include in vitro monolayer cell cultures, and in vivo animal models. These models have shortcomings when it comes to translating research about disorder pathology, development, and treatment to humans. Brain organoids are three-dimensional (3D) cultures of stem cell-derived neural cells that mimic the development of the in vivo human brain with high degrees of accuracy. Researchers have started developing these miniature brains to model neurodevelopment, and neuropathology. Brain organoids have been used to model a wide range of neurological disorders, including the complex and poorly understood neurodevelopmental and neurodegenerative disorders. In this review, we discuss the brain organoid technology, placing special focus on the different brain organoid models that have been developed, discussing their strengths, weaknesses, and uses in neurological disease modeling
Influence of Yb:YAG laser beam parameters on Haynes 188 weld fusion zone microstructure and mechanical properties
The weldability of 1.2 mm thick Haynes 188 alloy sheets by a disk Yb:YAG laser welding was examined. Butt joints were made, and the influence of parameters such as power, size, and shape of the spot, welding speed, and gas flow has been investigated. Based on an iconographic correlation approach, optimum process parameters were determined. Depending on the distribution of the power density (circular or annular), acceptable welds were obtained. Powers greater than 1700 W, welding speeds higher than 3.8 m mm1, and spot sizes between 160 and 320 lm were needed in the circular (small fiber) configuration. By comparison, the annular (large fiber) configuration required a power as high as 2500 W, and a welding speed less than 3.8 m min�1. The mechanical properties of the welds depended on their shape and microstructure, which in turn depended on the welding conditions. The content of carbides, the proportion of areas consisting of cellular and dendritic substructures, and the size of these substructures were used to explain the welded joint mechanical properties
Reprogramming the diseased brain
Direct conversion of astrocytes to dopamine neurons in vivo offers fresh optimism for the development of improved Parkinson's therapie
A Novel Gaussian Extrapolation Approach for 2D Gel Electrophoresis Saturated Protein Spots
Analysis of images obtained from two-dimensional gel electrophoresis (2D-GE) is a topic of utmost importance in bioinformatics research, since commercial and academic software available currently has proven to be neither completely effective nor fully automatic, often requiring manual revision and refinement of computer generated matches. In this work, we present an effective technique for the detection and the reconstruction of over-saturated protein spots. Firstly, the algorithm reveals overexposed areas, where spots may be truncated, and plateau regions caused by smeared and overlapping spots. Next, it reconstructs the correct distribution of pixel values in these overexposed areas and plateau regions, using a two-dimensional least-squares fitting based on a generalized Gaussian distribution. Pixel correction in saturated and smeared spots allows more accurate quantification, providing more reliable image analysis results. The method is validated for processing highly exposed 2D-GE images, comparing reconstructed spots with the corresponding non-saturated image, demonstrating that the algorithm enables correct spot quantification
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