Network Function Virtualization in Dynamic Networks: A Stochastic Perspective

This is the author accepted manuscript. The final version is available from IEEE via the DOI in this recordAs a key enabling technology for 5G network softwarization, Network Function Virtualization (NFV) provides an efficient paradigm to optimize network resource utility for the benefits of both network providers and users. However, the inherent network dynamics and uncertainties from 5G infrastructure, resources and applications are slowing down the further adoption of NFV in many emerging networking applications. Motivated by this, in this paper, we investigate the issues of network utility degradation when implementing NFV in dynamic networks, and design a proactive NFV solution from a fully stochastic perspective. Unlike existing deterministic NFV solutions, which assume given network capacities and/or static service quality demands, this paper explicitly integrates the knowledge of influential network variations into a twostage stochastic resource utilization model. By exploiting the hierarchical decision structures in this problem, a distributed computing framework with two-level decomposition is designed to facilitate a distributed implementation of the proposed model in large-scale networks. The experimental results demonstrate that the proposed solution not only improves 3∼5 folds of network performance, but also effectively reduces the risk of service quality violation.The work of Xiangle Cheng is partially supported by the China Scholarship Council for the study at the University of Exeter. This work is also partially supported by the UK EPSRC project (Grant No.: EP/R030863/1)

Phase-sensitive Manipulations of Squeezed Vacuum Field in an Optical Parametric Amplifier inside an Optical Cavity

Squeezed vacuum field can be amplified or deamplified when it is injected, as the signal beam, into a phase-sensitive optical parametric amplifier (OPA) inside an optical cavity. The spectral features of the reflected quantized signal field are controlled by the relative phase between the injected squeezed vacuum field and the pump field for the OPA. The experimental results demonstrate coherent phenomena of OPA in the quantum regime, and show phase-sensitive manipulations of quantum fluctuations for quantum information processing.Comment: 4 pages, 3 figures, appear in Phys. Rev. Let

Alterations in vasodilator-stimulated phosphoprotein (VASP) phosphorylation: associations with asthmatic phenotype, airway inflammation and β\u3csub\u3e2\u3c/sub\u3e-agonist use

Background Vasodilator-stimulated phosphoprotein (VASP) mediates focal adhesion, actin filament binding and polymerization in a variety of cells, thereby inhibiting cell movement. Phosphorylation of VASP via cAMP and cGMP dependent protein kinases releases this brake on cell motility. Thus, phosphorylation of VASP may be necessary for epithelial cell repair of damage from allergen-induced inflammation. Two hypotheses were examined: (1) injury from segmental allergen challenge increases VASP phosphorylation in airway epithelium in asthmatic but not nonasthmatic normal subjects, (2) regular in vivo β2-agonist use increases VASP phosphorylation in asthmatic epithelium, altering cell adhesion. Methods Bronchial epithelium was obtained from asthmatic and non-asthmatic normal subjects before and after segmental allergen challenge, and after regularly inhaled albuterol, in three separate protocols. VASP phosphorylation was examined in Western blots of epithelial samples. DNA was obtained for β2-adrenergic receptor haplotype determination. Results Although VASP phosphorylation increased, it was not significantly greater after allergen challenge in asthmatics or normals. However, VASP phosphorylation in epithelium of nonasthmatic normal subjects was double that observed in asthmatic subjects, both at baseline and after challenge. Regularly inhaled albuterol significantly increased VASP phosphorylation in asthmatic subjects in both unchallenged and antigen challenged lung segment epithelium. There was also a significant increase in epithelial cells in the bronchoalveolar lavage of the unchallenged lung segment after regular inhalation of albuterol but not of placebo. The haplotypes of the β2-adrenergic receptor did not appear to associate with increased or decreased phosphorylation of VASP. Conclusion Decreased VASP phosphorylation was observed in epithelial cells of asthmatics compared to nonasthmatic normals, despite response to β-agonist. The decreased phosphorylation does not appear to be associated with a particular β2-adrenergic receptor haplotype. The observed decrease in VASP phosphorylation suggests greater inhibition of actin reorganization which is necessary for altering attachment and migration required during epithelial repair

Persistent spin current in mesoscopic ferrimagnetic spin ring

Using a semiclassical approach, we study the persistent magnetization current of a mesoscopic ferrimagnetic ring in a nonuniform magnetic field. At zero temperature, there exists persistent spin current because of the quantum fluctuation of magnons, similar to the case of an antiferromagnetic spin ring. At low temperature, the current shows activation behavior because of the field-induced gap. At higher temperature, the magnitude of the spin current is proportional to temperature T, similar to the reported result of a ferromagnetic spin ring.Comment: 6 pages, 3 figures, one more reference adde

Tackling MARCKS-PIP3 circuit attenuates fibroblast activation and fibrosis progression.

Targeting activated fibroblasts, including myofibroblast differentiation, has emerged as a key therapeutic strategy in patients with idiopathic pulmonary fibrosis (IPF). However, there is no available therapy capable of selectively eradicating myofibroblasts or limiting their genesis. Through an integrative analysis of the regulator genes that are responsible for the activation of IPF fibroblasts, we noticed the phosphatidylinositol 4,5-bisphosphate (PIP2)-binding protein, myristoylated alanine-rich C-kinase substrate (MARCKS), as a potential target molecule for IPF. Herein, we have employed a 25-mer novel peptide, MARCKS phosphorylation site domain sequence (MPS), to determine if MARCKS inhibition reduces pulmonary fibrosis through the inactivation of PI3K/protein kinase B (AKT) signaling in fibroblast cells. We first observed that higher levels of MARCKS phosphorylation and the myofibroblast marker α-smooth muscle actin (α-SMA) were notably overexpressed in all tested IPF lung tissues and fibroblast cells. Treatment with the MPS peptide suppressed levels of MARCKS phosphorylation in primary IPF fibroblasts. A kinetic assay confirmed that this peptide binds to phospholipids, particularly PIP2, with a dissociation constant of 17.64 nM. As expected, a decrease of phosphatidylinositol (3,4,5)-trisphosphate pools and AKT activity occurred in MPS-treated IPF fibroblast cells. MPS peptide was demonstrated to impair cell proliferation, invasion, and migration in multiple IPF fibroblast cells in vitro as well as to reduce pulmonary fibrosis in bleomycin-treated mice in vivo. Surprisingly, we found that MPS peptide decreases α-SMA expression and synergistically interacts with nintedanib treatment in IPF fibroblasts. Our data suggest MARCKS as a druggable target in pulmonary fibrosis and also provide a promising antifibrotic agent that may lead to effective IPF treatments.-Yang, D. C., Li, J.-M., Xu, J., Oldham, J., Phan, S. H., Last, J. A., Wu, R., Chen, C.-H. Tackling MARCKS-PIP3 circuit attenuates fibroblast activation and fibrosis progression

Phosphine-Catalyzed Annulations of Azomethine Imines: Allene-Dependent [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] Pathways

In this paper we describe the phosphine-catalyzed [3 + 2], [3 + 3], [4 + 3], and [3 + 2 + 3] annulations of azomethine imines and allenoates. These processes mark the first use of azomethine imines in nucleophilic phosphine catalysis, producing dinitrogen-fused heterocycles, including tetrahydropyrazolo-pyrazolones, -pyridazinones, -diazepinones, and -diazocinones. Counting the two different reaction modes in the [3 + 3] cyclizations, there are five distinct reaction pathways—the choice of which depends on the structure and chemical properties of the allenoate. All reactions are operationally simple and proceed smoothly under mild reaction conditions, affording a broad range of 1,2-dinitrogen-containing heterocycles in moderate to excellent yields. A zwitterionic intermediate formed from a phosphine and two molecules of ethyl 2,3-butadienoate acted as a 1,5-dipole in the annulations of azomethine imines, leading to the [3 + 2 + 3] tetrahydropyrazolo-diazocinone products. The incorporation of two molecules of an allenoate into an eight-membered-ring product represents a new application of this versatile class of molecules in nucleophilic phosphine catalysis. The salient features of this protocol—the facile access to a diverse range of nitrogen-containing heterocycles and the simple preparation of azomethine imine substrates—suggest that it might find extensive applications in heterocycle synthesis

The East-Asian VLBI Network

The East-Asian VLBI Network (EAVN) is the international VLBI facility in East Asia and is conducted in collaboration with China, Japan, and Korea. The EAVN consists of VLBI arrays operated in each East Asian country, containing 21 radio telescopes and three correlators. The EAVN will be mainly operated at 6.7 (C-band), 8 (X-band), 22 (K-band), and 43 GHz (Q-band), although the EAVN has an ability to conduct observations at 1.6 - 129 GHz. We have conducted fringe test observations eight times to date at 8 and 22 GHz and fringes have been successfully detected at both frequencies. We have also conducted science commissioning observations of 6.7 GHz methanol masers in massive star-forming regions. The EAVN will be operational from the second half of 2017, providing complementary results with the FAST on AGNs, massive star-forming regions, and evolved stars with high angular resolution at cm- to mm-wavelengths.Comment: 6 pages, 3 figures, 2 tables. To appear in the proceedings of "Frontiers in Radio Astronomy and FAST Early Sciences Symposium 2015" ed. Lei Qian (ASP Conf. Ser.

Hydrogen peroxide contributes to the ultraviolet-B (280-315 nm) induced oxidative stress of plant leaves through multiple pathways

Solar UV-B (280-315 nm) radiation is a developmental signal in plants but may also cause oxidative stress when combined with other environmental factors. Using computer modelling and in solution experiments we show that UV-B is capable of photosensitizing hydroxyl radical production from hydrogen peroxide. We present evidence that the oxidative effect of UV-B in leaves is at least two-fold: (i) it increases cellular hydrogen peroxide concentrations, to a larger extent in pyridoxine antioxidant mutant pdx1.3-1 Arabidopsis and (ii) is capable of a partial photo-conversion of both ‘natural’ and ‘extra’ hydrogen peroxide to hydroxyl radicals. As stress conditions other than UV can increase cellular hydrogen peroxide levels, synergistic deleterious effects of various stresses may be expected already under ambient solar UV-B