RESUMO
We describe the design and implementation of a stable high-power 1064 nm laser system to generate optical lattices for experiments with ultracold quantum gases. The system is based on a low-noise laser amplified by an array of four heavily modified, high-power fiber amplifiers. The beam intensity is stabilized and controlled with a nonlinear feedback loop. Using real-time monitoring of the resulting optical lattice, we find the stability of the lattice site positions to be well below the lattice spacing over the course of hours. The position of the harmonic trap produced by the Gaussian envelope of the lattice beams is stable to about one lattice spacing and the long-term (six-month) relative root-mean-square stability of the lattice spacing itself is 0.5%.
RESUMO
The vessel wall is composed of distinct cellular layers, yet communication among individual cells within and between layers results in a dynamic and versatile structure. The morphogenesis of the normal vascular wall involves a highly regulated process of cell proliferation, migration, and differentiation. The use of modern developmental biological and genetic approaches has markedly enriched our understanding of the molecular and cellular mechanisms underlying these developmental events. Additionally, the application of similar approaches to study diverse vascular diseases has resulted in paradigm-shifting insights into pathogenesis. Further investigations into the biology of vascular cells in development and disease promise to have major ramifications on therapeutic strategies to combat pathologies of the vasculature.
Assuntos
Vasos Sanguíneos/citologia , Doenças Vasculares/fisiopatologia , Animais , Diferenciação Celular , Movimento Celular , Proliferação de Células , HumanosRESUMO
We perform a quantitative simulation of the repulsive Fermi-Hubbard model using an ultracold gas trapped in an optical lattice. The entropy of the system is determined by comparing accurate measurements of the equilibrium double occupancy with theoretical calculations over a wide range of parameters. We demonstrate the applicability of both high-temperature series and dynamical mean-field theory to obtain quantitative agreement with the experimental data. The reliability of the entropy determination is confirmed by a comprehensive analysis of all systematic errors. In the center of the Mott insulating cloud we obtain an entropy per atom as low as 0.77k(B) which is about twice as large as the entropy at the Néel transition. The corresponding temperature depends on the atom number and for small fillings reaches values on the order of the tunneling energy.
RESUMO
Leukocyte adhesion to vascular endothelium under flow involves an adhesion cascade consisting of multiple receptor pairs that may function in an overlapping fashion. P-selectin glycoprotein ligand-1 (PSGL-1) and L-selectin have been implicated in neutrophil adhesion to P- and E-selectin under flow conditions. To study, in isolation, the interaction of PSGL-1 with P- and E-selectin under flow, we developed an in vitro model in which various recombinant regions of extracellular PSGL-1 were coupled to 10-microm-diameter microspheres. In a parallel plate chamber with well defined flow conditions, live time video microscopy analyses revealed that microspheres coated with PSGL-1 attached and rolled on 4-h tumor necrosis factor-alpha-activated endothelial cell monolayers, which express high levels of E-selectin, and CHO monolayers stably expressing E- or P-selectin. Further studies using CHO-E and -P monolayers demonstrate that the first 19 amino acids of PSGL-1 are sufficient for attachment and rolling on both E- and P-selectin and suggest that a sialyl Lewis x-containing glycan at Threonine-16 is critical for this sequence of amino acids to mediate attachment to E- and P-selectin. The data also demonstrate that a sulfated, anionic polypeptide segment within the amino terminus of PSGL-1 is necessary for PSGL-1-mediated attachment to P- but not to E-selectin. In addition, the results suggest that PSGL-1 has more than one binding site for E-selectin: one site located within the first 19 amino acids of PSGL-1 and one or more sites located between amino acids 19 through 148.
Assuntos
Adesão Celular/fisiologia , Selectina E/metabolismo , Endotélio Vascular/citologia , Glicoproteínas de Membrana/metabolismo , Selectina-P/metabolismo , Animais , Células CHO , Cricetinae , Humanos , Fragmentos Fc das Imunoglobulinas/genética , Ligantes , Glicoproteínas de Membrana/genética , Metaloendopeptidases/metabolismo , Microesferas , Neuraminidase/metabolismo , Oligossacarídeos/metabolismo , Proteínas Recombinantes de Fusão , Antígeno Sialil Lewis X , Treonina/metabolismo , Fator de Necrose Tumoral alfa/farmacologia , Veias UmbilicaisRESUMO
This study tests Eysenck's psychophysiological hypotheses concerning the relationship between intellectual performance and personality type. The data originated from two partial samples with N = 314. The personality types were distinguished with the ENNR-Questionnaire. The intellectual performance was tested using items which are based on Jäger's factor analytic studies. 23 differentially complex items stemed from the main intelligence factors, and separate measures for speed and quality were used to test the hypotheses. The results of all analyses of variancy falsify Eysenck's hypotheses. The "neurotic introverts" showed the worst results in both quality and speed by most of the items, independent of complexity and intelligence factor (chi-square-test of positional frequency). The "stable" and "neurotic extraverts" showed the best results.