Spatio-temporal operator formalism for holographic recording and diffraction in a photorefractive-based true-time-delay phased-array processor

We present a spatio-temporal operator formalism and beam propagation simulations that describe the broadband efficient adaptive method for a true-time-delay array processing (BEAMTAP) algorithm for an optical beamformer by use of a photorefractive crystal. The optical system consists of a tapped-delay line implemented with an acoustooptic Bragg cell, an accumulating scrolling time-delay detector achieved with a traveling-fringes detector, and a photorefractive crystal to store the adaptive spatio-temporal weights as volume holographic gratings. In this analysis, linear shift-invariant integral operators are used to describe the propagation, interference, grating accumulation, and volume holographic diffraction of the spatio-temporally modulated optical fields in the system to compute the adaptive array processing operation. In addition, it is shown that the random fluctuation in time and phase delays of the optically modulated and transmitted array signals produced by fiber perturbations (temperature fluctuations, vibrations, or bending) are dynamically compensated for through the process of holographic wavefront reconstruction as a byproduct of the adaptive beam-forming and jammer-excision operation. The complexity of the cascaded spatial-temporal integrals describing the holographic formation, and subsequent readout processes, is shown to collapse to a simple imaging condition through standard operator manipulation. We also present spatio-temporal beam propagation simulation results as an illustrative demonstration of our analysis and the operation of a BEAMTAP beamformer.     

Rapid and Superior Bacteria Killing of Carbon Quantum Dots/ZnO Decorated Injectable Folic Acid‐Conjugated PDA Hydrogel through Dual‐Light Triggered ROS and Membrane Permeability

One of the most difficult challenges in the biomedical field is bacterial infection, which causes tremendous harm to human health. In this work, an injectable hydrogel is synthesized through rapid assembly of dopamine (DA) and folic acid (FA) cross‐linked by transition metal ions (TMIs, i.e., Zn²⁺), which was named as DFT‐hydrogel. Both the two carboxyl groups in the FA molecule and catechol in polydopamine (PDA) easily chelates Zn²⁺ to form metal–ligand coordination, thereby allowing this injectable hydrogel to match the shapes of wounds. In addition, PDA in the hydrogel coated around carbon quantum dot‐decorated ZnO (C/ZnO) nanoparticles (NPs) to rapidly generate reactive oxygen species (ROS) and heat under illumination with 660 and 808 nm light, endows this hybrid hydrogel with great antibacterial efficacy against Staphylococcus aureus (S. aureus, typical Gram‐positive bacteria) and Escherichia coli (E. coli, typical Gram‐negative bacteria). The antibacterial efficacy of the prepared DFT‐C/ZnO‐hydrogel against S. aureus and E. coli under dual‐light irradiation is 99.9%. Importantly, the hydrogels release zinc ions over 12 days, resulting in a sustained antimicrobial effect and promoted fibroblast growth. Thus, this hybrid hydrogel exhibits great potential for the reconstruction of bacteria‐infected tissues, especially exposed wounds.     

Assessment of different techniques for quantification of α-Al(FeMn)Si and β-AlFeSi intermetallics in AA 6xxx alloys

During homogenisation of AA 6xxx aluminium alloys, the platelike β-AlFeSi intermetallic phase will transform to a less Si-rich and more spheroidised α-Al(FeMn)Si phase which is more favourable for extrusion. In this study, several quantitative methods, which determine the relative volume fraction of α-Al(FeMn)Si and β-AlFeSi, are compared and an assessment of each method is made. The methods used are optical microscopy, scanning electron microscopy (SEM) in combination with electron dispersive X-ray (EDX) using polished samples, and X-ray diffraction (XRD) on intermetallics, extracted through selective dissolution of the Al matrix. The highest accuracy is obtained by using SEM/EDX analysis and applying two criteria.     

Optoelectronic implementation of a 256-channel sonar adaptive-array processor

We present an optoelectronic implementation of an adaptive-array processor that is capable of performing beam forming and jammer nulling in signals of wide fractional bandwidth that are detected by an array of arbitrary topology. The optical system makes use of a two-dimensional scrolling spatial light modulator to represent an array of input signals in 256 tapped delay lines, two acousto-optic modulators for modulating the feedback error signal, and a photorefractive crystal for representing the adaptive weights as holographic gratings. Gradient-descent learning is used to dynamically adapt the holographic weights to optimally form multiple beams and to null out multiple interference sources, either in the near field or in the far field. Space-integration followed by differential heterodyne detection is used for generating the system's output. The processor is analyzed to show the effects of exponential weight decay on the optimum solution and on the convergence conditions. Several experimental results are presented that validate the system's capacity for broadband beam forming and jammer nulling for linear and circular arrays.     

In situ observations of chemically induced grain-boundary migration and discontinuous precipitation in the aluminum-zinc system

In situ observations are reported for chemically induced grain-boundary migration (CIGM) and discontinuous precipitation (DP) in the Al-Zn system. In each case, it is found that the migration of the grain boundary is a steady continuous process, at least on the scale of the resolution of the electron optical techniques employed. However, there are significant differences; the grain-boundary velocities are such that a diffusion field must exist in the parent crystal for the case of CIGM but little or no volume diffusion penetration for steady DP. For CIGM, it is argued that the coherency strain energy in the diffusion field is sufficient for the development of a small residual chemical force; for steady DP, a large fraction of the total chemical force is available to act directly across the grain boundary. In the latter case, agreement is obtained between observed and calculated dynamic boundary shapes, using a method in which the chemical force (corrected for losses due to continuous precipitation in the parent phase) is balanced against capillary forces. Formerly with McMaster University     

Antibodies to orthopoxvirus in domestic cats in Norway

Hemangiomata is the more frequent pediatric tumor, absent at birth and usually growing, sometimes very quickly, during the first week of life. It potentially represents a serious problem because of his unforeseeable evolution during the time: is it more useful to use a corticosteroid therapy or to wait for the involution of the tumor? Here we have the results of the treatment on 51 babies who presented with hemangiomas of various sites: 52.6% of the lesions were on the face and head, 13.4% on chest wall, 10% on upper limbs, 4% on abdominal wall, 10% on pelvis region and 10% multiple. Therapy was compression in 10% of patients, corticosteroid injection in 66%, oral administered corticosteroid in 12%, surgery post corticosteroid therapy in 11.5%, others in 2.5%. Best results were obtained on the lesion of the head and face (good in 96%), worst in those of the abdomen (any modification in 100%).     

Cytokine profiles differ in newly recruited and resident subsets of mucosal macrophages from inflammatory bowel disease

BACKGROUND & AIMS: Most macrophages in the normal intestinal mucosa have a mature phenotype. In inflammatory bowel disease (IBD), a monocyte-like subset (CD14+ L1+) accumulates. The aim of this study was to characterize its potential with regard to cytokines. METHODS: Lamina propria mononuclear cells were adherence-separated, with or without depletion of CD14+ cells, and production of cytokines was investigated by bioassay, enzyme-linked immunosorbent assay, or immunocytochemistry. RESULTS: Tumor necrosis factor alpha (TNF-alpha), interleukin 1beta (IL-1beta), and IL-1 receptor antagonist were found mainly in cells positive for myelomonocytic L1. In undepleted IBD cultures, TNF-alpha, IL-1alpha and beta, and IL-10 were markedly up-regulated by pokeweed mitogen stimulation; IL-1alpha and beta and IL-10 were also up-regulated by stimulation of interferon gamma and lipopolysaccharide in combination. The latter stimulation had no effect on normal control or CD14-depleted IBD cultures. Indomethacin caused a marked increase of TNF-alpha, particularly in undepleted IBD cultures, whereas IL-10 and IL-4 decreased TNF-alpha and IL-1beta in both CD14+ and CD14 macrophages. CONCLUSIONS: In IBD mucosa, macrophages with a monocyte-like phenotype are primed for production of TNF-alpha and IL-1alpha/beta and may therefore be of significant pathogenic importance [corrected]. However, this CD14+ subset, as well as the mucosal resident macrophages, have preserved responsiveness to several down-regulatory factors such as the macrophage deactivators IL-10 and IL-4.     

A glycosylated Bence Jones protein and its autologous amyloid light chain containing potentially amyloidogenic residues

Amyloidosis is characterized by deposition of protein fibrils in various tissues. The wide variety of sequences of both amyloidogenic and non-amyloidogenic immunoglobulin light chains makes them a unique tool for addressing the importance of primary structure in the formation of insoluble fibrils. In this study, we have determined the primary structure of the kappa I immunoglobulin light chain from both the urinary Bence Jones protein and the deposited amyloid fibrils of a patient (MH) with primary amyloidosis. The sequence identity of urinary-excreted and tissue-deposited light chains excluded biclonality and somatic mutations and confirmed that the light chain existed in both a soluble and an insoluble form. Several residues have been previously reported to be significantly associated with amyloidogenic kappa chains. Many of these were found in the MH sequence, including Asp31, Asn45, Phe49, Gln55, His70, Asn/Gly93 and ProN/Val96, thereby supporting their potential role in fibrillogenesis. In addition, Asn20 and Pro60 of protein MH replaced the normally conserved Thr20 and Ser60. Asn20 was glycosylated in both the Bence Jones and the amyloid fibril protein MH. Cumulative effects of amyloid-associated residues and glycosylation might have rendered the immunoglobulin light chain MH prone to fibril formation.     

Identification of RANTES receptors on human monocytic cells: competition for binding and desensitization by homologous chemotactic cytokines

RANTES (regulated on activation, normal T expressed and secreted) is a member of the chemotactic cytokine (chemokine) beta subfamily. High affinity receptors for RANTES have been identified on a human monocytic leukemia cell line THP-1, which responded to RANTES in chemotaxis and calcium mobilization assays. Steady-state binding data analyses revealed approximately 700 binding sites/cell on THP-1 cells with a Kd value of 400 pM, comparable to that expressed on human peripheral blood monocytes. The RANTES binding to monocytic cells was competed for by monocyte chemotactic and activating factor (MCAF) and macrophage inflammatory protein 1 (MIP-1) alpha, two other chemokine beta cytokines. Although MCAF and MIP-1 alpha competed for RANTES binding to monocytes with apparent lower affinity (with estimated Kd of 6 and 1.6, nM respectively) both of these cytokines effectively desensitized the calcium mobilization induced by RANTES. The chemotactic response of THP-1 cells to RANTES was also markedly inhibited by preincubation with MCAF or MIP-1 alpha. In contrast, RANTES did not desensitize the THP-1 calcium mobilization and chemotaxis in response to MCAF or MIP-1 alpha. These results, together with our previous observations that RANTES did not compete for MCAF or MIP-1 alpha binding on monocytic cells, indicate the expression of promiscuous receptors on monocytes that recognize one or more cytokines within the chemokine beta family.