More Harvard humbug.

Replies to J. Sonnenfeld's (1982) critique of D. Bramel and R. Friend's (see record 1982-08638-001) article on the studies performed at the Hawthorne plant of Western Electric. Sonnenfeld fails to recognize the unique aspects of Bramel and Friend's reinterpretation of what happened at Hawthorne. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Three-dimensional finite-element analysis of laminated composites

A three-dimensional finite-element analysis treating the mechanical response of thick laminated composite plates in bending is presented. An isoparametric solid element with a cubic displacement expansion in planform and a linear variation through the thickness is used to model each layer of the laminate. The degrees-of-freedom of the element are retained at its boundaries so that interconnections between lamina with different fiber orientations can be made at their interfaces. An incore version of the conjugate gradient technique, which does not have bandwidth restrictions, is used to minimize the total potential energy of the system with the number of iterations to convergence being about one-fifth the total global degrees-of-freedom. Because a three-dimensional analysis is used, the effects of thickness-stretching, transverse shear, extension, and bending deformations are obtained. Comparisons with three-dimensional elasticity solutions are in excellent agreement and show the necessity of having individual elements for each layer when they have different fiber orientations and when the plates are thick.     

Conditioned suppression of humoral immunity in the rat.

180 Charles River rats were conditioned by pairing consumption of a novel sodium saccharin drinking solution with the effects of an ip injection of 75 mg/kg cyclophosphamide, an immunosuppressive drug. Five and 10 days after conditioning, an experimental group (Group CS) was reexposed to the saccharin drinking solution. Control Ss (Group CSo) were conditioned but were not reexposed to saccharin. On Days 10, 15, or 25 after conditioning, Ss were injected ip with sheep erythrocytes, and independent subgroups were sampled for hemagglutinating antibody titer 4, 6, or 8 days later. Antibody titers 4 days after immunization were lower than values observed 6 and 8 days after immunization, and CS Ss had an attenuated antibody response. There were no significant differences between Group CSo and a group of placebo-treated Ss, but CS Ss had lower antibody titers than placebo-treated animals 4, 6, and 8 days after antigenic stimulation. Results suggest that reexposure to a CS may have long-lasting effects, and provide further documentation of conditioned immunopharmacologic effects and the impact of behavioral factors in modifying immunologic reactivity. (16 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Designing mobile technologies to support co-present collaboration

Mobile technologies offer new opportunities for childrens educational activities in that they can be used across different locations and times. Naturally, some instances of mobile technology use will necessitate, or be enhanced by, the sharing of information. Social interaction is important for sharing ideas, constructing and shaping understanding and fundamental for educational development. However the physical size of mobile technologies presents interesting challenges when designing for collaborative activities. When designing mobile technologies the importance of collaborative tasks has often been overlooked. The replacement of low-tech artefacts with digital devices, for supporting multiple users, can inhibit the shareability of information. We present three projects where mobile technologies have been used as part of a larger mixed reality experience. Novel technologies were used to support childrens collaborative activities in storytelling, an adventure game and during an outdoor field trip. Interaction with mobile devices within each project is reviewed and the authors highlight important considerations for their design and use across multiple contexts.     

A miniature photorefractive circuit for principal component extraction

The optical feature extractor is a photorefractive ring oscillator that can identify the strongest spatiotemporal component of its input space. The theoretical sections discuss the design and performance limitations of the signal extractor. A simple model of the filter's nonlinear functioning enables the reader to go directly to the experimental section that describes the making of the filter and experimental results. The device, also called the auto-tuning filter, is 5 cm2 in size, has a 3 GHz processing bandwidth, and requires less than 5 mW of continuous optical power to operate.     

Metabolomic Evidence for Peroxisomal Dysfunction in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a chronic and debilitating disease characterized by unexplained physical fatigue, cognitive and sensory dysfunction, sleeping disturbances, orthostatic intolerance, and gastrointestinal problems. People with ME/CFS often report a prodrome consistent with infections. Using regression, Bayesian and enrichment analyses, we conducted targeted and untargeted metabolomic analysis of plasma from 106 ME/CFS cases and 91 frequency-matched healthy controls. Subjects in the ME/CFS group had significantly decreased levels of plasmalogens and phospholipid ethers (p < 0.001), phosphatidylcholines (p < 0.001) and sphingomyelins (p < 0.001), and elevated levels of dicarboxylic acids (p = 0.013). Using machine learning algorithms, we were able to differentiate ME/CFS or subgroups of ME/CFS from controls with area under the receiver operating characteristic curve (AUC) values up to 0.873. Our findings provide the first metabolomic evidence of peroxisomal dysfunction, and are consistent with dysregulation of lipid remodeling and the tricarboxylic acid cycle. These findings, if validated in other cohorts, could provide new insights into the pathogenesis of ME/CFS and highlight the potential use of the plasma metabolome as a source of biomarkers for the disease.     

Essential requirement of cytosolic phospholipase A2 for activation of the phagocyte NADPH oxidase

Arachidonic acid (AA) can trigger activation of the phagocyte NADPH oxidase in a cell-free assay. However, a role for AA in activation of the oxidase in intact cells has not been established, nor has the AA generating enzyme critical to this process been identified. The human myeloid cell line PLB-985 was transfected to express p85 cytosolic phospholipase A2 (cPLA2) antisense mRNA and stable clones were selected that lack detectable cPLA2. cPLA2-deficient PLB-985 cells differentiate similarly to control PLB-985 cells in response to retinoic acid or 1,25-dihydroxyvitamin D3, indicating that cPLA2 is not involved in the differentiation process. Neither cPLA2 nor stimulated [3H]AA release were detectable in differentiated cPLA2-deficient PLB-985 cells, demonstrating that cPLA2 is the major type of PLA2 activated in phagocytic-like cells. Despite the normal synthesis of NADPH oxidase subunits during differentiation of cPLA2-deficient PLB-985 cells, these cells fail to activate NADPH oxidase in response to a variety of soluble and particulate stimuli, but the addition of exogenous AA fully restores oxidase activity. This establishes an essential requirement of cPLA2-generated AA for activation of phagocyte NADPH oxidase.     

Synthesis and characterization of new poly(ethylene glycol)bisphosphonate vinylic monomer and non-fluorescent and NIR-fluorescent bisphosphonate micrometer-sized particles

Bisphosphonates (BPs) are non-hydrolysable pyrophosphate analogs with high affinity to hydroxyapatite (HAP, the main inorganic ingredient in bones) and are mainly used for bone diseases treatments.A new stable PEG-BP monomer and particles have been prepared for enhanced long term bone-targeted imaging and therapy applications. The new formed BP particles possess dual functionalities: chelation to the bone mineral, HAP, through the BP groups and covalent attachment of a dye or drug through primary amine groups.The BP particles showed no cytotoxic effect on human osteosarcoma cell lines and minor toxicity on mouse macrophage cells, indicating that these BP particles are good candidates for in vivo testing. The BP monomer and particles exhibited inhibition of HAP formation and dissolution, similar to a commercial Alendronate. Near IR (NIR) fluorescent BP particles were obtained by conjugation of Cy7-NHS ester to the primary amine groups of the BP particles.     

Chemical Solution Deposition of Columnar-Grained Metallic Lanthanum Nitrate Thin Films

Columnar and (100)-oriented LaNiO₃ thin films were prepared on silicon substrates by a chemical solution deposition (CSD) process using a 0.05 M solution. By reducing the individual layer thickness to 10 nm, columnar LaNiO₃ films with a lateral grain size of ∼120 nm were obtained. The success of this approach required restricting the individual layer thickness to a value below the grain size observed for equiaxed films. This change in microstructure resulted in an improvement in conductivity. The columnar LaNiO₃ film with a thickness of 300 nm showed a resistivity of 4.5 × 10⁻⁵Ω·cm, which is lower by one order of magnitude than that of fine-grain equiaxed films that typically result from CSD methods.     

Novel NGR anchored pullulan micelles for controlled and targeted delivery of doxorubicin to HeLa cancerous cells

Doxorubicin (DOX) is used to treat different kinds of cancers, including cervix carcinoma. However, it has various side effects such as cardiotoxicity. Nano-sized controlled releasing carriers such as polymeric micelles are of interesting approaches to overcome these side effects of doxorubicin in cancer chemotherapy. Regarding the up-regulation of CD13/APN receptors on the cervix carcinoma cells, which can bind to peptide sequences specially NGR (asparagine–glycine–arginine) with high affinity, peptide sequence (NGR) targeted micelles would lead to effective treatment of this carcinoma. In this study, the NGR peptide sequence was synthesized using the solution-phase strategy from asparagine, glycine, and arginine residues. The pullulan–retinoic acid conjugate and pullulan–retinoic acid–NGR conjugate were prepared by the amide and ester bond formation between the hydroxyl groups of pullulan and carboxylic acid groups of retinoic acid and peptide sequence. Pullulan–retinoic acid–NGR micelles were prepared by the direct dissolution method. The optimized micelles, according to their particle size (124.5 nm), zeta potential (? 3.65 mV), entrapment efficiency (85%), and release of DOX (70%, within 72 h) were assessed for their cytotoxicity on HeLa cells using MTT assay. NGR-targeted pullulan/retinoic acid micelles had higher cytotoxicity than the free DOX in cell culture studies on the HeLa cell line, and this can be a promising result in the treatment of cervix carcinoma.