Bloch oscillations of Bose-Einstein condensates: Breakdown and revival

We investigate the dynamics of Bose-Einstein condensates (BEC) in a tilted one-dimensional periodic lattice within the mean-field (Gross-Pitaevskii) description. Unlike in the linear case the Bloch oscillations decay because of nonlinear dephasing. Pronounced revival phenomena are observed. These are analyzed in detail in terms of a simple integrable model constructed by an expansion in Wannier-Stark resonance states. We also briefly discuss the pulsed output of such systems for stronger static fields.Comment: RevTeX4, 9 pages, 14 figure

Chaotic Quantum Decay in Driven Biased Optical Lattices

Quantum decay in an ac driven biased periodic potential modeling cold atoms in optical lattices is studied for a symmetry broken driving. For the case of fully chaotic classical dynamics the classical exponential decay is quantum mechanically suppressed for a driving frequency \omega in resonance with the Bloch frequency \omega_B, q\omega=r\omega_B with integers q and r. Asymptotically an algebraic decay ~t^{-\gamma} is observed. For r=1 the exponent \gamma agrees with $q$ as predicted by non-Hermitian random matrix theory for q decay channels. The time dependence of the survival probability can be well described by random matrix theory. The frequency dependence of the survival probability shows pronounced resonance peaks with sub-Fourier character.Comment: 7 pages, 5 figure

Bound and resonance states of the nonlinear Schroedinger equation in simple model systems

The stationary nonlinear Schroedinger equation, or Gross-Pitaevskii equation, is studied for the cases of a single delta potential and a delta-shell potential. These model systems allow analytical solutions, and thus provide useful insight into the features of stationary bound, scattering and resonance states of the nonlinear Schroedinger equation. For the single delta potential, the influence of the potential strength and the nonlinearity is studied as well as the transition from bound to scattering states. Furthermore, the properties of resonance states for a repulsive delta-shell potential are discussed.Comment: 19 pages, 10 figure

INCENTIVO AO ESTUDO ATRAVÉS DOS JOGOS: EXPERIÊNCIAS NO DESENVOLVIMENTO DE UMA REDE SOCIAL GAMIFICADA

  Com o rápido e crescente uso da tecnologia, as crianças já nascem imergidas neste ambiente digitalizado, atuando de uma forma muito natural ao lidar com diversos tipos de tecnologias. A rede social é uma delas. Ela disponibiliza informação e interação sobre todo tipo de conteúdo para o usuário, também como a possibilidade de compartilhamento de conteúdo por parte do usuário. O projeto apresentado neste artigo estuda essa tecnologia para estimular e ajudar no reforço escolar, por meio de jogos para dispositivos móveis - bem como o compartilhamento das informações em uma Rede Social Gamificada. Postula-se, um empenho dos usuários através de suas conquistas e pontuações nos jogos educativos que fazem parte da Rede Social Gamificada, denominada Teia. Resultados preliminares do projeto foram mostrados no SBGames e no Gamepad, ambos no ano de 2013

Elevated arginine levels in liver tumors promote metabolic reprogramming and tumor growth

Arginine auxotropy, due to reduced expression of urea cycle genes, is common in cancer. However, little is known about the levels of arginine in these cancers. Here, we report that arginine levels are elevated in hepatocellular carcinoma (HCC) despite reduced expression of urea cycle enzymes. Liver tumors accumulate high levels specifically of arginine via increased uptake and, more importantly, via suppression of arginine-to-polyamine conversion due to reduced arginase 1 (ARG1) and agmatinase (AGMAT) expression. Furthermore, the high levels of arginine are required for tumor growth. Mechanistically, high levels of arginine promote tumorigenesis via transcriptional regulation of metabolic genes, including upregulation of asparagine synthetase (ASNS). ASNS-derived asparagine further enhances arginine uptake, creating a positive feedback loop to sustain high arginine levels and oncogenic metabolism. Thus, arginine is a novel second messenger-like molecule that reprograms metabolism to promote tumor growth

MicroRNA-100-5p and microRNA-298-5p released from apoptotic cortical neurons are endogenous Toll-like receptor 7/8 ligands that contribute to neurodegeneration

Background: MicroRNA (miRNA) expression in the brain is altered in neurodegenerative diseases. Recent studies demonstrated that selected miRNAs conventionally regulating gene expression at the post-transcriptional level can act extracellularly as signaling molecules. The identity of miRNA species serving as membrane receptor ligands involved in neuronal apoptosis in the central nervous system (CNS), as well as the miRNAs' sequence and structure required for this mode of action remained largely unresolved. Methods. Using a microarray-based screening approach we analyzed apoptotic cortical neurons of C56BL/6 mice and their supernatant with respect to alterations in miRNA expression/presence. HEK-Blue Toll-like receptor (TLR) 7/8 reporter cells, primary microglia and macrophages derived from human and mouse were employed to test the potential of the identified miRNAs released from apoptotic neurons to serve as signaling molecules for the RNA-sensing receptors. Biophysical and bioinformatical approaches, as well as immunoassays and sequential microscopy were used to analyze the interaction between candidate miRNA and TLR. Immunocytochemical and -histochemical analyses of murine CNS cultures and adult mice intrathecally injected with miRNAs, respectively, were performed to evaluate the impact of miRNA-induced TLR activation on neuronal survival and microglial activation. Results: We identified a specific pattern of miRNAs released from apoptotic cortical neurons that activate TLR7 and/or TLR8, depending on sequence and species. Exposure of microglia and macrophages to certain miRNA classes released from apoptotic neurons resulted in the sequence-specific production of distinct cytokines/chemokines and increased phagocytic activity. Out of those miRNAs miR-100-5p and miR-298-5p, which have consistently been linked to neurodegenerative diseases, entered microglia, located to their endosomes, and directly bound to human TLR8. The miRNA-TLR interaction required novel sequence features, but no specific structure formation of mature miRNA. As a consequence of miR-100-5p- and miR-298-5p-induced TLR activation, cortical neurons underwent cell-autonomous apoptosis. Presence of miR-100-5p and miR-298-5p in cerebrospinal fluid led to neurodegeneration and microglial accumulation in the murine cerebral cortex through TLR7 signaling. Conclusion: Our data demonstrate that specific miRNAs are released from apoptotic cortical neurons, serve as endogenous TLR7/8 ligands, and thereby trigger further neuronal apoptosis in the CNS. Our findings underline the recently discovered role of miRNAs as extracellular signaling molecules, particularly in the context of neurodegeneration

Cc Chemokine Receptor (Ccr)3/Eotaxin Is Followed by Ccr4/Monocyte-Derived Chemokine in Mediating Pulmonary T Helper Lymphocyte Type 2 Recruitment after Serial Antigen Challenge in Vivo

Isolated peripheral blood CD4 cells from allergic individuals express CC chemokine receptor (CCR)3 and CCR4 after expansion in vitro. In addition, human T helper type 2 (Th2) cells polarized in vitro selectively express CCR3 and CCR4 at certain stages of activation/differentiation and respond preferentially to the ligands eotaxin and monocyte-derived chemokine (MDC). However, controversy arises when the in vivo significance of this distinct expression is discussed. To address the functional role of CCR3/eotaxin and CCR4/MDC during the in vivo recruitment of Th2 cells, we have transferred effector Th cells into naive mice to induce allergic airway disease. Tracking of these cells after repeated antigen challenge has established that both CCR3/eotaxin and CCR4/MDC axes contribute to the recruitment of Th2 cells to the lung, demonstrating the in vivo relevance of the expression of these receptors on Th2 cells. We have shown that involvement of the CCR3/eotaxin pathway is confined to early stages of the response in vivo, whereas repeated antigen stimulation results in the predominant use of the CCR4/MDC pathway. We propose that effector Th2 cells respond to both CCR3/eotaxin and CCR4/MDC pathways initially, but that a progressive increase in CCR4-positive cells results in the predominance of the CCR4/MDC axis in the long-term recruitment of Th2 cells in vivo

Desenvolvimento e Aplicação do CDA Introdução aos Estudos Virtuais

O presente trabalho tem o objetivo de mostrar o processo de desenvolvimento de um construto digital de aprendizagem criado pelo Laboratório de Objetos de Aprendizagem da Universidade Feevale. O artigo introduz autores que sustentam o uso de jogos digitais na educação e que serviram para embasar a metodologia utilizada na criação e validação do construto. Os resultados foram obtidos através da aplicação do projeto em um grupo de 101 estudantes dos cursos a distância da própria instituição