185 research outputs found
Non-affine geometrization can lead to nonphysical instabilities
Geometrization of dynamics consists of representing trajectories by geodesics
on a configuration space with a suitably defined metric. Previously, efforts
were made to show that the analysis of dynamical stability can also be carried
out within geometrical frameworks, by measuring the broadening rate of a bundle
of geodesics. Two known formalisms are via Jacobi and Eisenhart metrics. We
find that this geometrical analysis measures the actual stability when the
length of any geodesic is proportional to the corresponding time interval. We
prove that the Jacobi metric is not always an appropriate parametrization by
showing that it predicts chaotic behavior for a system of harmonic oscillators.
Furthermore, we show, by explicit calculation, that the correspondence between
dynamical- and geometrical-spread is ill-defined for the Jacobi metric. We find
that the Eisenhart dynamics corresponds to the actual tangent dynamics and is
therefore an appropriate geometrization scheme.Comment: Featured on the Cover of the Journal. 9 pages, 6 figures:
http://iopscience.iop.org/1751-8121/48/7/07510
Density of States of Quantum Spin Systems from Isotropic Entanglement
We propose a method which we call "Isotropic Entanglement" (IE), that
predicts the eigenvalue distribution of quantum many body (spin) systems (QMBS)
with generic interactions. We interpolate between two known approximations by
matching fourth moments. Though, such problems can be QMA-complete, our
examples show that IE provides an accurate picture of the spectra well beyond
what one expects from the first four moments alone. We further show that the
interpolation is universal, i.e., independent of the choice of local terms.Comment: 4+ pages, content is as in the published versio
Unfrustrated Qudit Chains and their Ground States
We investigate chains of 'd' dimensional quantum spins (qudits) on a line
with generic nearest neighbor interactions without translational invariance. We
find the conditions under which these systems are not frustrated, i.e. when the
ground states are also the common ground states of all the local terms in the
Hamiltonians. The states of a quantum spin chain are naturally represented in
the Matrix Product States (MPS) framework. Using imaginary time evolution in
the MPS ansatz, we numerically investigate the range of parameters in which we
expect the ground states to be highly entangled and find them hard to
approximate using our MPS method.Comment: 5 pages, 5 figures. Typos correcte
Elevated InsP3R expression underlies enhanced calcium fluxes and spontaneous extra-systolic calcium release events in hypertrophic cardiac myocytes
Cardiac hypertrophy is associated with profound remodeling of Ca(2+) signaling pathways. During the early, compensated stages of hypertrophy, Ca(2+) fluxes may be enhanced to facilitate greater contraction, whereas as the hypertrophic heart decompensates, Ca(2+) homeostatic mechanisms are dysregulated leading to decreased contractility, arrhythmia and death. Although ryanodine receptor Ca(2+) release channels (RyR) on the sarcoplasmic reticulum (SR) intracellular Ca(2+) store are primarily responsible for the Ca(2+) flux that induces myocyte contraction, a role for Ca(2+) release via the inositol 1,4,5-trisphosphate receptor (InsP(3)R) in cardiac physiology has also emerged. Specifically, InsP(3)-induced Ca(2+) signals generated following myocyte stimulation with an InsP(3)-generating agonist (e.g., endothelin, ET-1), lead to modulation of Ca(2+) signals associated with excitation-contraction coupling (ECC) and the induction of spontaneous Ca(2+) release events that cause cellular arrhythmia. Using myocytes from spontaneously hypertensive rats (SHR), we recently reported that expression of the type 2 InsP(3)R (InsP(3)R2) is significantly increased during hypertrophy. Notably, this increased expression was restricted to the junctional SR in close proximity to RyRs. There, enhanced Ca(2+) release via InsP(3)Rs serves to sensitize neighboring RyRs causing an augmentation of Ca(2+) fluxes during ECC as well as an increase in non-triggered Ca(2+) release events. Although the sensitization of RyRs may be a beneficial consequence of elevated InsP(3)R expression during hypertrophy, the spontaneous Ca(2+) release events are potentially of pathological significance giving rise to cardiac arrhythmia. InsP(3)R2 expression was also increased in hypertrophic hearts from patients with ischemic dilated cardiomyopathy and aortically-banded mice demonstrating that increased InsP(3)R expression may be a general phenomenon that underlies Ca(2+) changes during hypertrophy
Error analysis of free probability approximations to the density of states of disordered systems
Theoretical studies of localization, anomalous diffusion and ergodicity
breaking require solving the electronic structure of disordered systems. We use
free probability to approximate the ensemble- averaged density of states
without exact diagonalization. We present an error analysis that quantifies the
accuracy using a generalized moment expansion, allowing us to distinguish
between different approximations. We identify an approximation that is accurate
to the eighth moment across all noise strengths, and contrast this with the
perturbation theory and isotropic entanglement theory.Comment: 5 pages, 3 figures, submitted to Phys. Rev. Let
A human coronavirus responsible for the common cold massively kills dendritic cells but not monocytes
Copyright @ 2012, American Society for Microbiology.Human coronaviruses are associated with upper respiratory tract infections that occasionally spread to the lungs and other organs. Although airway epithelial cells represent an important target for infection, the respiratory epithelium is also composed of an elaborate network of dendritic cells (DCs) that are essential sentinels of the immune system, sensing pathogens and presenting foreign antigens to T lymphocytes. In this report, we show that in vitro infection by human coronavirus 229E (HCoV-229E) induces massive cytopathic effects in DCs, including the formation of large syncytia and cell death within only few hours. In contrast, monocytes are much more resistant to infection and cytopathic effects despite similar expression levels of CD13, the membrane receptor for HCoV-229E. While the differentiation of monocytes into DCs in the presence of granulocyte-macrophage colony-stimulating factor and interleukin-4 requires 5 days, only 24 h are sufficient for these cytokines to sensitize monocytes to cell death and cytopathic effects when infected by HCoV-229E. Cell death induced by HCoV-229E is independent of TRAIL, FasL, tumor necrosis factor alpha, and caspase activity, indicating that viral replication is directly responsible for the observed cytopathic effects. The consequence of DC death at the early stage of HCoV-229E infection may have an impact on the early control of viral dissemination and on the establishment of long-lasting immune memory, since people can be reinfected multiple times by HCoV-229E
QUALITY OF REFRIGERATED RAW MILK FROM BUFFALO COWS (Bubalus bubalis bubalis) IN DIFFERENT FARMS AND SEASONS IN BRAZIL
T lymphocytes isolated from patients with advanced colorectal cancer are suitable for gene immunotherapy approaches
Direct observation shows superposition and large scale flexibility within cytoplasmic dynein motors moving along microtubules
Cytoplasmic dynein is a dimeric AAA+ motor protein that performs critical roles in eukaryotic cells by moving along microtubules using ATP. Here using cryo-electron microscopy we directly observe the structure of Dictyostelium discoideum dynein dimers on microtubules at near-physiological ATP concentrations. They display remarkable flexibility at a hinge close to the microtubule binding domain (the stalkhead) producing a wide range of head positions. About half the molecules have the two heads separated from one another, with both leading and trailing motors attached to the microtubule. The other half have the two heads and stalks closely superposed in a front-to-back arrangement of the AAA+ rings, suggesting specific contact between the heads. All stalks point towards the microtubule minus end. Mean stalk angles depend on the separation between their stalkheads, which allows estimation of inter-head tension. These findings provide a structural framework for understanding dynein’s directionality and unusual stepping behaviour
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Over expression of Plk1 does not induce cell division in rat cardiac myocytes in vitro
BACKGROUND: Mammalian cardiac myocytes withdraw from the cell cycle during post-natal development, resulting in a non-proliferating, fully differentiated adult phenotype that is unable to repair damage to the myocardium, such as occurs following a myocardial infarction. We and others previously have shown that forced expression of certain cell cycle molecules in adult cardiac myocytes can promote cell cycle progression and division in these cells. The mitotic serine/threonine kinase, Polo-like kinase-1 (Plk1), is known to phosphorylate and activate a number of mitotic targets, including Cdc2/Cyclin B1, and to promote cell division. PRINCIPAL FINDINGS: The mammalian Plk family are all differentially regulated during the development of rat cardiac myocytes, with Plk1 showing the most dramatic decrease in both mRNA, protein and activity in the adult. We determined the potential of Plk1 to induce cell cycle progression and division in cultured rat cardiac myocytes. A persistent and progressive loss of Plk1 expression was observed during myocyte development that correlated with the withdrawal of adult rat cardiac myocytes from the cell cycle. Interestingly, when Plk1 was over-expressed in cardiac myocytes by adenovirus infection, it was not able to promote cell cycle progression, as determined by cell number and percent binucleation. CONCLUSIONS: We conclude that, in contrast to Cdc2/Cyclin B1 over-expression, the forced expression of Plk1 in adult cardiac myocytes is not sufficient to induce cell division and myocardial repair
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