Impact of anisotropy on vortex clusters and their dynamics

We investigate the effects of anisotropy on the stability and dynamics of vortex cluster states which arise in Bose-Einstein condensates. Sufficiently strong anisotropies are shown to stabilize states with arbitrary numbers of vortices that are highly unstable in the isotropic limit. Conversely, anisotropy can be used to destabilize states which are stable in the isotropic limit. Near the linear limit, we identify the bifurcations of vortex states including their emergence from linear eigenstates, while in the strongly nonlinear limit, a particle-like description of the dynamics of the vortices in the anisotropic trap is developed. Both are in very good agreement with numerical results. Collective modes of stabilized many vortex cluster states are demonstrated.Comment: 6 pages, 6 figure

Ruimte voor Rechtsvorming:een onderzoek naar adequate instrumenten voor afhandeling en rechtsvorming door de Afdeling bestuursrechtspraak van de Raad van State

De Afdeling bestuursrechtspraak van de Raad van State is zowel geschilbeslechter als rechtsvormer. Haar geschilbeslechtende taak ontleent de Afdeling aan het feit dat overheid en burgers royaal gebruik maken van de mogelijkheid hun geschil ter beoordeling aan haar voor te leggen. De taak van de Afdeling als rechtsvormer vloeit voort uit haar hoedanigheid van hoogste bestuursrechter. Tussen beide taken bestaat een inherente spanning. De wens om elke afzonderlijke (hoger)beroepszaak zo gedegen, snel en effectief mogelijk af te handelen, kan in strijd komen met de noodzaak om de rechtsvormende taak als hoogste bestuursrechter inhoud te geven. In dit boek is de vraag aan de orde hoe de procedure bij de Afdeling bestuursrecht-spraak zo kan worden vormgegeven, dat beide taken het volle pond krijgen. Daartoe is zowel in kaart gebracht op welke wijze de Afdeling de aan haar voorgelegde ge-schillen behandelt, als ook welke alternatieven er zijn voor de wijze waarop de afhan-deling van (met name) hogerberoepszaken op dit moment is georganiseerd. Het onderzoek biedt daarmee niet alleen een uniek beeld van de werkwijze van de Afdeling bestuursrechtspraak, maar ook een grondige inventarisatie van een mogelij-ke alternatieve vormgeving van de procedure van (hoger) beroep. Het onderzoek mondt uit in een aantal aanbevelingen die beogen te bewerkstelligen dat de ruimte voor rechtsvorming wordt vergroot, zonder dat dit ten koste gaat van een snelle en effectieve beslechting van geschillen door de Afdeling bestuursrechtspraak van de Raad van State

TREatment of ATopic eczema (TREAT) Registry Taskforce: consensus on how and when to measure the core dataset for atopic eczema treatment research registries.

BackgroundComparative, real-life and long-term evidence on the effectiveness and safety of phototherapy and systemic therapy in moderate-to-severe atopic eczema (AE) is limited. Such data must come from well-designed prospective patient registries. Standardization of data collection is needed for direct comparisons and data pooling.ObjectivesTo reach a consensus on how and when to measure the previously defined domain items of the TREatment of ATopic eczema (TREAT) Registry Taskforce core dataset for research registries for paediatric and adult patients with AE.MethodsProposals for the measurement instruments were based on recommendations of the Harmonising Outcome Measures for Eczema (HOME) initiative, the existing AE database of TREATgermany, systematic reviews of the literature and expert opinions. The proposals were discussed at three face-to-face consensus meetings, one teleconference and via e-mail. The frequency of follow-up visits was determined by an expert survey.ResultsA total of 16 experts from seven countries participated in the 'how to measure' consensus process and 12 external experts were consulted. A consensus was reached for all domain items on how they should be measured by assigning measurement instruments. A minimum follow-up frequency of initially 4 weeks after commencing treatment, then every 3 months while on treatment and every 6 months while off treatment was defined.ConclusionsThis core dataset for national AE research registries will aid in the comparability and pooling of data across centres and country borders, and enables international collaboration to assess the long-term effectiveness and safety of phototherapy and systemic therapy used in patients with AE. What's already known about this topic? Comparable, real-life and long-term data on the effectiveness and safety of phototherapy and systemic therapy in patients with atopic eczema (AE) are needed. There is a high diversity of outcomes and instruments used in AE research, which require harmonization to enhance comparability and allow data pooling. What does this study add? Our taskforce has reached international consensus on how and when to measure core domain items for national AE research registries. This core dataset is now available for use by researchers worldwide and will aid in the collection of unified data. What are the clinical implications of this work? The data collected through this core dataset will help to gain better insights into the long-term effectiveness and safety of phototherapy and systemic therapy in AE and will provide important information for clinical practice. Standardization of such data collection at the national level will also allow direct data comparisons and pooling across country borders (e.g. in the analysis of treatment-related adverse events that require large patient numbers)

Embedded macrophages induce intravascular coagulation in 3D blood vessel-on-chip

Macrophages are innate immune cells that prevent infections and help in wound healing and vascular inflammation. While these cells are natural helper cells, they also contribute to chronic diseases, e.g., by infiltrating the endothelial layer in early atherosclerosis and by promoting vascular inflammation. There is a crosstalk between inflammatory pathways and key players in thrombosis, such as platelets and endothelial cells – a phenomenon known as ‘thromboinflammation’. The role of the embedded macrophages in thromboinflammation in the context of vascular disease is incompletely understood. Blood vessels-on-chips, which are microfluidic vascular cell culture models, have been used extensively to study aspects of vascular disease, like permeability, immune cell adhesion and thrombosis. Blood perfusion assays in blood vessel-on-chip models benefit from multiple unique aspects of the models, such as control of microvessel structure and well-defined flow patterns, as well as the ability to perform live imaging. However, due to their simplified nature, blood vessels-on-chip models have not yet been used to capture the complex cellular crosstalk that is important in thromboinflammation. Using induced pluripotent stem cell-derived endothelial cells and polarized THP-1 monocytes, we have developed and systematically set up a 3D blood vessel-on-chip with embedded (lipid-laden) macrophages, which is created using sequential cell seeding in viscous finger patterned collagen hydrogels. We have set up a human whole blood perfusion assay for these 3D blood vessels-on-chip. An increased deposition of fibrin in the blood vessel-on-chip models containing lipid-laden macrophages was observed. We anticipate the future use of this advanced vascular in vitro model in drug development for early atherosclerosis or aspects of other vascular diseases

Sperm DNA damage causes genomic instability in early embryonic development

Genomic instability is common in human embryos, but the underlying causes are largely unknown. Here, we examined the consequences of sperm DNA damage on the embryonic genome by single-cell whole-genome sequencing of individual blastomeres from bovine embryos produced with sperm damaged by γ-radiation. Sperm DNA damage primarily leads to fragmentation of the paternal chromosomes followed by random distribution of the chromosomal fragments over the two sister cells in the first cell division. An unexpected secondary effect of sperm DNA damage is the induction of direct unequal cleavages, which include the poorly understood heterogoneic cell divisions. As a result, chaotic mosaicism is common in embryos derived from fertilizations with damaged sperm. The mosaic aneuploidies, uniparental disomies, and de novo structural variation induced by sperm DNA damage may compromise fertility and lead to rare congenital disorders when embryos escape developmental arrest