148 research outputs found
Instabilities in crystal growth by atomic or molecular beams
The planar front of a growing a crystal is often destroyed by instabilities.
In the case of growth from a condensed phase, the most frequent ones are
diffusion instabilities, which will be but briefly discussed in simple terms in
chapter II. The present review is mainly devoted to instabilities which arise
in ballistic growth, especially Molecular Beam Epitaxy (MBE). The reasons of
the instabilities can be geometric (shadowing effect), but they are mostly
kinetic or thermodynamic. The kinetic instabilities which will be studied in
detail in chapters IV and V result from the fact that adatoms diffusing on a
surface do not easily cross steps (Ehrlich-Schwoebel or ES effect). When the
growth front is a high symmetry surface, the ES effect produces mounds which
often coarsen in time according to power laws. When the growth front is a
stepped surface, the ES effect initially produces a meandering of the steps,
which eventually may also give rise to mounds. Kinetic instabilities can
usually be avoided by raising the temperature, but this favours thermodynamic
instabilities. Concerning these ones, the attention will be focussed on the
instabilities resulting from slightly different lattice constants of the
substrate and the adsorbate. They can take the following forms. i) Formation of
misfit dislocations (chapter VIII). ii) Formation of isolated epitaxial
clusters which, at least in their earliest form, are `coherent' with the
substrate, i.e. dislocation-free (chapter X). iii) Wavy deformation of the
surface, which is presumably the incipient stage of (ii) (chapter IX). The
theories and the experiments are critically reviewed and their comparison is
qualitatively satisfactory although some important questions have not yet
received a complete answer.Comment: 90 pages in revtex, 45 figures mainly in gif format. Review paper to
be published in Physics Reports. Postscript versions for all the figures can
be found at http://www.theo-phys.uni-essen.de/tp/u/politi
Identification of Mechanosensitive Genes during Embryonic Bone Formation
Although it is known that mechanical forces are needed for normal bone
development, the current understanding of how biophysical stimuli are
interpreted by and integrated with genetic regulatory mechanisms is limited.
Mechanical forces are thought to be mediated in cells by
“mechanosensitive” genes, but it is a challenge to
demonstrate that the genetic regulation of the biological system is dependant on
particular mechanical forces in vivo. We propose a new means of selecting
candidate mechanosensitive genes by comparing in vivo gene expression patterns
with patterns of biophysical stimuli, computed using finite element analysis. In
this study, finite element analyses of the avian embryonic limb were performed
using anatomically realistic rudiment and muscle morphologies, and patterns of
biophysical stimuli were compared with the expression patterns of four candidate
mechanosensitive genes integral to bone development. The expression patterns of
two genes, Collagen X (ColX) and Indian hedgehog (Ihh), were shown to colocalise
with biophysical stimuli induced by embryonic muscle contractions, identifying
them as potentially being involved in the mechanoregulation of bone formation.
An altered mechanical environment was induced in the embryonic chick, where a
neuromuscular blocking agent was administered in ovo to modify skeletal muscle
contractions. Finite element analyses predicted dramatic changes in levels and
patterns of biophysical stimuli, and a number of immobilised specimens exhibited
differences in ColX and Ihh expression. The results obtained indicate that
computationally derived patterns of biophysical stimuli can be used to inform a
directed search for genes that may play a mechanoregulatory role in particular
in vivo events or processes. Furthermore, the experimental data demonstrate that
ColX and Ihh are involved in mechanoregulatory pathways and may be key mediators
in translating information from the mechanical environment to the molecular
regulation of bone formation in the embryo
The North Atlantic Waveguide and Downstream Impact Experiment
The North Atlantic Waveguide and Downstream Impact Experiment (NAWDEX) explored the impact of diabatic processes on disturbances of the jet stream and their influence on downstream high-impact weather through the deployment of four research aircraft, each with a sophisticated set of remote sensing and in situ instruments, and coordinated with a suite of ground-based measurements. A total of 49 research flights were performed, including, for the first time, coordinated flights of the four aircraft: the German High Altitude and Long Range Research Aircraft (HALO), the Deutsches Zentrum für Luft- und Raumfahrt (DLR) Dassault Falcon 20, the French Service des Avions Français Instrumentés pour la Recherche en Environnement (SAFIRE) Falcon 20, and the British Facility for Airborne Atmospheric Measurements (FAAM) BAe 146. The observation period from 17 September to 22 October 2016 with frequently occurring extratropical and tropical cyclones was ideal for investigating midlatitude weather over the North Atlantic. NAWDEX featured three sequences of upstream triggers of waveguide disturbances, as well as their dynamic interaction with the jet stream, subsequent development, and eventual downstream weather impact on Europe. Examples are presented to highlight the wealth of phenomena that were sampled, the comprehensive coverage, and the multifaceted nature of the measurements. This unique dataset forms the basis for future case studies and detailed evaluations of weather and climate predictions to improve our understanding of diabatic influences on Rossby waves and the downstream impacts of weather systems affecting Europe
Synaptic Maturation at Cortical Projections to the Lateral Amygdala in a Mouse Model of Rett Syndrome
Rett syndrome (RTT) is a neuro-developmental disorder caused by loss of function of Mecp2 - methyl-CpG-binding protein 2 - an epigenetic factor controlling DNA transcription. In mice, removal of Mecp2 in the forebrain recapitulates most of behavioral deficits found in global Mecp2 deficient mice, including amygdala-related hyper-anxiety and lack of social interaction, pointing a role of Mecp2 in emotional learning. Yet very little is known about the establishment and maintenance of synaptic function in the adult amygdala and the role of Mecp2 in these processes. Here, we performed a longitudinal examination of synaptic properties at excitatory projections to principal cells of the lateral nucleus of the amygdala (LA) in Mecp2 mutant mice and their wild-type littermates. We first show that during animal life, Cortico-LA projections switch from a tonic to a phasic mode, whereas Thalamo-LA synapses are phasic at all ages. In parallel, we observed a specific elimination of Cortico-LA synapses and a decrease in their ability of generating presynaptic long term potentiation. In absence of Mecp2, both synaptic maturation and synaptic elimination were exaggerated albeit still specific to cortical projections. Surprisingly, associative LTP was unaffected at Mecp2 deficient synapses suggesting that synaptic maintenance rather than activity-dependent synaptic learning may be causal in RTT physiopathology. Finally, because the timing of synaptic evolution was preserved, we propose that some of the developmental effects of Mecp2 may be exerted within an endogenous program and restricted to synapses which maturate during animal life
CD83 Modulates B Cell Function In Vitro: Increased IL-10 and Reduced Ig Secretion by CD83Tg B Cells
The murine transmembrane glycoprotein CD83 is an important regulator for both thymic T cell maturation and peripheral T cell responses. Recently, we reported that CD83 also has a function on B cells: Ubiquitous transgenic (Tg) expression of CD83 interfered with the immunoglobulin (Ig) response to infectious agents and to T cell dependent as well as T cell independent model antigen immunization. Here we compare the function of CD83Tg B cells that overexpress CD83 and CD83 mutant (CD83mu) B cells that display a drastically reduced CD83 expression. Correlating with CD83 expression, the basic as well as the lipopolysaccharide (LPS) induced expression of the activation markers CD86 and MHC-II are significantly increased in CD83Tg B cells and reciprocally decreased in CD83mu B cells. Wild-type B cells rapidly upregulate CD83 within three hours post BCR or TLR engagement by de novo protein synthesis. The forced premature overexpression of CD83 on the CD83Tg B cells results in reduced calcium signaling, reduced Ig secretion and a reciprocally increased IL-10 production upon in vitro activation. This altered phenotype is mediated by CD83 expressed on the B cells themselves, since it is observed in the absence of accessory cells. In line with this finding, purified CD83mu B cells displayed a reduced IL-10 production and slightly increased Ig secretion upon LPS stimulation in vitro. Taken together, our data strongly suggest that CD83 is expressed by B cells upon activation and contributes to the regulation of B cell function
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A genome-wide association study of anorexia nervosa
Anorexia nervosa (AN) is a complex and heritable eating disorder characterized by dangerously low body weight. Neither candidate gene studies nor an initial genome wide association study (GWAS) have yielded significant and replicated results. We performed a GWAS in 2,907 cases with AN from 14 countries (15 sites) and 14,860 ancestrally matched controls as part of the Genetic Consortium for AN (GCAN) and the Wellcome Trust Case Control Consortium 3 (WTCCC3). Individual association analyses were conducted in each stratum and meta-analyzed across all 15 discovery datasets. Seventy-six (72 independent) SNPs were taken forward for in silico (two datasets) or de novo (13 datasets) replication genotyping in 2,677 independent AN cases and 8,629 European ancestry controls along with 458 AN cases and 421 controls from Japan. The final global meta-analysis across discovery and replication datasets comprised 5,551 AN cases and 21,080 controls. AN subtype analyses (1,606 AN restricting; 1,445 AN binge-purge) were performed. No findings reached genome-wide significance. Two intronic variants were suggestively associated: rs9839776 (P=3.01×10−7) in SOX2OT and rs17030795 (P=5.84×10−6) in PPP3CA. Two additional signals were specific to Europeans: rs1523921 (P=5.76×10−6) between CUL3 and FAM124B and rs1886797 (P=8.05×10−6) near SPATA13. Comparing discovery to replication results, 76% of the effects were in the same direction, an observation highly unlikely to be due to chance (P= 4×10−6), strongly suggesting that true findings exist but that our sample, the largest yet reported, was underpowered for their detection. The accrual of large genotyped AN case-control samples should be an immediate priority for the field
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
J. Kaprio, A. Palotie, A. Raevuori-Helkamaa ja S. Ripatti ovat työryhmän Eating Disorders Working Group of the Psychiatric Genomics Consortium jäseniä. Erratum in: Sci Rep. 2017 Aug 21;7(1):8379, doi: 10.1038/s41598-017-06409-3We conducted a genome-wide association study (GWAS) of anorexia nervosa (AN) using a stringently defined phenotype. Analysis of phenotypic variability led to the identification of a specific genetic risk factor that approached genome-wide significance (rs929626 in EBF1 (Early B-Cell Factor 1); P = 2.04 x 10(-7); OR = 0.7; 95% confidence interval (CI) = 0.61-0.8) with independent replication (P = 0.04), suggesting a variant-mediated dysregulation of leptin signaling may play a role in AN. Multiple SNPs in LD with the variant support the nominal association. This demonstrates that although the clinical and etiologic heterogeneity of AN is universally recognized, further careful sub-typing of cases may provide more precise genomic signals. In this study, through a refinement of the phenotype spectrum of AN, we present a replicable GWAS signal that is nominally associated with AN, highlighting a potentially important candidate locus for further investigation.Peer reviewe
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