1,224 research outputs found
On the Virialization of Disk Winds: Implications for the Black Hole Mass Estimates in AGN
Estimating the mass of a supermassive black hole (SMBH) in an active galactic
nucleus (AGN) usually relies on the assumption that the broad line region (BLR)
is virialized. However, this assumption seems invalid in BLR models that
consists of an accretion disk and its wind. The disk is likely Keplerian and
therefore virialized. However, the wind material must, beyond a certain point,
be dominated by an outward force that is stronger than gravity. Here, we
analyze hydrodynamic simulations of four different disk winds: an isothermal
wind, a thermal wind from an X-ray heated disk, and two line-driven winds, one
with and the other without X-ray heating and cooling. For each model, we check
whether gravity governs the flow properties, by computing and analyzing the
volume-integrated quantities that appear in the virial theorem: internal,
kinetic, and gravitational energies, We find that in the first two models, the
winds are non-virialized whereas the two line-driven disk winds are virialized
up to a relatively large distance. The line-driven winds are virialized because
they accelerate slowly so that the rotational velocity is dominant and the wind
base is very dense. For the two virialized winds, the so-called projected
virial factor scales with inclination angle as . Finally, we
demonstrate that an outflow from a Keplerian disk becomes unvirialized more
slowly when it conserves the gas specific angular momentum -- as in the models
considered here, than when it conserves the angular velocity -- as in the
so-called magneto-centrifugal winds.Comment: Accepted to Ap
Learning in neural networks with material synapses
We discuss the long term maintenance of acquired memory in synaptic connections of a perpetually learning electronic device. This is affected by ascribing each synapse a finite number of stable states in which it can maintain for indefinitely long periods. Learning uncorrelated stimuli is expressed as a stochastic process produced by the neural activities on the synapses. In several interesting cases the stochastic process can be analyzed in detail, leading to a clarification of the performance of the network, as an associative memory, during the process of uninterrupted learning. The stochastic nature of the process and the existence of an asymptotic distribution for the synaptic values in the network imply generically that the memory is a palimpsest but capacity is as low as log N for a network of N neurons. The only way we find for avoiding this tight constraint is to allow the parameters governing the learning process (the coding level of the stimuli; the transition probabilities for potentiation and depression and the number of stable synaptic levels) to depend on the number of neurons. It is shown that a network with synapses that have two stable states can dynamically learn with optimal storage efficiency, be a palimpsest, and maintain its (associative) memory for an indefinitely long time provided the coding level is low and depression is equilibrated against potentiation. We suggest that an option so easily implementable in material devices would not have been overlooked by biology. Finally we discuss the stochastic learning on synapses with variable number of stable synaptic states
Microscopic approach to orientational order of domain walls
We develop a fully microscopic, statistical mechanics approach to study phase
transitions in Ising systems with competing interactions at different scales.
Our aim is to consider orientational and positional order parameters in a
unified framework. In this work we consider two dimensional stripe forming
systems, where nematic, smectic and crystal phases are possible. We introduce a
nematic order parameter in a lattice, which measures orientational order of
interfaces. We develop a mean field approach which leads to a free energy which
is a function of both the magnetization (density) and the orientational
(nematic) order parameters. Self-consistent equations for the order parameters
are obtained and the solutions are described for a particular system, the
Dipolar Frustrated Ising Ferromagnet. We show that this system has an
Ising-nematic phase at low temperatures in the square lattice, where positional
order (staggered magnetization) is zero. At lower temperatures a crystal-stripe
phase may appear. In the continuum limit the present approach connects to a
Ginsburg-Landau theory, which has an isotropic-nematic phase transition with
breaking of a continuous symmetry.Comment: 9 pages, 7 figures, revised and expanded, published versio
Near-inertial kinetic energy budget of the mixed layer and shear evolution in the transition layer in the Arabian Sea during the monsoons
Author Posting. © American Geophysical Union, 2015. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research: Oceans 120 (2015): 6492–6507, doi:10.1002/2014JC010198.We present the horizontal kinetic energy (KE) balance of near-inertial currents in the mixed layer and explain shear evolution in the transition layer using observations from a mooring at 15.26° N in the Arabian Sea during the southwest monsoon. The highly sheared and stratified transition layer at the mixed-layer base varies between 5 m and 35 m and correlates negatively with the wind stress. Results from the mixed layer near-inertial KE (NIKE) balance suggest that wind energy at times can energize the transition layer and at other times is fully utilized within the mixed layer. A simple two layer model is utilized to study the shear evolution in the transition layer and shown to match well with observations. The shear production in this model arises from alignment of wind stress and shear. Although the winds are unidirectional during the monsoon, the shear in the transition layer is predominantly near-inertial. The near-inertial shear bursts in the observations show the same phasing and magnitude at near-inertial frequencies as the wind-shear alignment term.NASA Grant Number: NNX12AD47G, NSF Grant Number: 0928138, ONR Grant Numbers: N00014-11-1-0429 and N00014-10-1-0273, NSF Grant Number: OCE-07455082016-03-2
Role of renin-angiotensin system blockade in atherosclerotic renal artery stenosis and renovascular hypertension
Ischemic dual papillary muscle rupture in a postpartum patient with vascular Ehlers-Danlos syndrome
Specific Soluble Oligomers of Amyloid-β Peptide Undergo Replication and Form Non-Fibrillar Aggregates in Interfacial Environments
Aggregates of amyloid-β (Aβ) peptides have been implicated in the etiology of Alzheimer disease. Among the different forms of Aβ aggregates, low molecular weight species ranging between ∼2- and 50-mers, also called “soluble oligomers,” have emerged as the species responsible for early synaptic dysfunction and neuronal loss. Emerging evidence suggests that the neurotoxic oligomers need not be formed along the obligatory nucleation-dependant fibril formation pathway. In our earlier work, we reported the isolation of one such “off-pathway” 12–18-mer species of Aβ42 generated from fatty acids called large fatty acid-derived oligomers (LFAOs) (Kumar, A., Bullard, R. L., Patel, P., Paslay, L. C., Singh, D., Bienkiewicz, E. A., Morgan, S. E., and Rangachari, V. (2011) PLoS One 6, e18759). Here, we report the physiochemical aspects of LFAO-monomer interactions as well as LFAO-LFAO associations in the presence of interfaces. We discovered that LFAOs are a replicating strain of oligomers that recruit Aβ42 monomers and quantitatively convert them into LFAO assemblies at the expense of fibrils, a mechanism similar to prion propagation. We also found that in the presence of hexane-buffer or chloroform-buffer interfaces LFAOs are able to associate with themselves to form larger but non-fibrillar aggregates. These results further support the hypothesis that low molecular weight oligomers can be generated via non-fibril formation pathways. Furthermore, the unique replicating property of off-pathway oligomers may hold profound significance for Alzheimer disease pathology
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BIM Mediates EGFR Tyrosine Kinase Inhibitor-Induced Apoptosis in Lung Cancers with Oncogenic EGFR Mutations
Background: Epidermal growth factor receptor (EGFR) mutations are present in the majority of patients with non-small cell lung cancer (NSCLC) responsive to the EGFR tyrosine kinase inhibitors (TKIs) gefitinib or erlotinib. These EGFR-dependent tumors eventually become TKI resistant, and the common secondary T790M mutation accounts for half the tumors with acquired resistance to gefitinib. However, the key proapoptotic proteins involved in TKI-induced cell death and other secondary mutations involved in resistance remain unclear. The objective of this study was to identify the mechanism of EGFR TKI-induced apoptosis and secondary resistant mutations that affect this process.
Methods and Findings: To study TKI-induced cell death and mechanisms of resistance, we used lung cancer cell lines (with or without EGFR mutations), Ba/F3 cells stably transfected with EGFR mutation constructs, and tumor samples from a gefitinib-resistant patient. Here we show that up-regulation of the BH3-only polypeptide BIM (also known as BCL2-like 11) correlated with gefitinib-induced apoptosis in gefitinib-sensitive EGFR-mutant lung cancer cells. The T790M mutation blocked gefitinib-induced up-regulation of BIM and apoptosis. This blockade was overcome by the irreversible TKI CL-387,785. Knockdown of BIM by small interfering RNA was able to attenuate apoptosis induced by EGFR TKIs. Furthermore, from a gefitinib-resistant patient carrying the
activating L858R mutation, we identified a novel secondary resistant mutation, L747S in cis to the activating mutation, which attenuated the up-regulation of BIM and reduced apoptosis.
Conclusions: Our results provide evidence that BIM is involved in TKI-induced apoptosis in sensitive EGFRmutant cells and that both attenuation of the up-regulation of BIM and resistance to gefitinibinduced apoptosis are seen in models that contain the common EGFR T790M and the novel L747S secondary resistance mutations. These findings also suggest that induction of BIM may have a role in the treatment of TKI-resistant tumors
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Complement Activation in Patients With Probable Systemic Lupus Erythematosus and Ability to Predict Progression to American College of Rheumatology-Classified Systemic Lupus Erythematosus.
ObjectiveTo evaluate the frequency of cell-bound complement activation products (CB-CAPs) as a marker of complement activation in patients with suspected systemic lupus erythematosus (SLE) and the usefulness of this biomarker as a predictor of the evolution of probable SLE into SLE as classified by the American College of Rheumatology (ACR) criteria.MethodsPatients in whom SLE was suspected by lupus experts and who fulfilled 3 ACR classification criteria for SLE (probable SLE) were enrolled, along with patients with established SLE as classified by both the ACR and the Systemic Lupus International Collaborating Clinics (SLICC) criteria, patients with primary Sjögren's syndrome (SS), and patients with other rheumatic diseases. Individual CB-CAPs were measured by flow cytometry, and positivity rates were compared to those of commonly assessed biomarkers, including serum complement proteins (C3 and C4) and autoantibodies. The frequency of a positive multianalyte assay panel (MAP), which includes CB-CAPs, was also evaluated. Probable SLE cases were followed up prospectively.ResultsThe 92 patients with probable SLE were diagnosed more recently than the 53 patients with established SLE, and their use of antirheumatic medications was lower. At the enrollment visit, more patients with probable SLE were positive for CB-CAPs (28%) or MAP (40%) than had low complement levels (9%) (P = 0.0001 for each). In probable SLE, MAP scores of >0.8 at enrollment predicted fulfillment of a fourth ACR criterion within 18 months (hazard ratio 3.11, P < 0.01).ConclusionComplement activation occurs in some patients with probable SLE and can be detected with higher frequency by evaluating CB-CAPs and MAP than by assessing traditional serum complement protein levels. A MAP score above 0.8 predicts transition to classifiable SLE according to ACR criteria
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