Low-temperature scanning electron microscopy in fungus-nematode interaction

A comparative study has been made of different preparation techniques used for the scanning electron microscope (SEM), with regard to their application to fungus-nematode interaction. The preparation of frozen-hydrated specimens of both healthy and Arthrobotrys-oli-gospora-infected second-stage larvae of the root-knot nematode (Meloidogyne sp.) is described, and the results are compared with those obtained by critical point-drying and freeze-drying. In all cases the frozen-hydrated specimens consistently showed the best preservation.     

Truncated activin type II receptors inhibit bioactivity by the formation of heteromeric complexes with activin type I. receptors

Truncated activin type II receptors have been reported to inhibit activin receptor signaling in Xenopus embryos, although the mechanism of action for this effect has not been fully understood. In the present study we demonstrate that in P19 embryonal carcinoma cells both the induction of the activin responsive 3TP-lux reporter construct and the inhibition of retinoic acid-induced neuronal differentiation by activin are blocked by expression of a truncated activin receptor. To reveal the mechanism of action of truncated activin receptors, the interaction between different activin receptors has been investigated upon coexpression in COS cells followed by cross-linking of 125I-activin A and subsequent immunoprecipitation. Complexes between a truncated activin type IIA receptor and activin type IA and type IB receptors can be formed, as demonstrated by coimmunoprecipitation of these type I receptors with the truncated activin type IIA receptor. Other type I receptors known as ALK-1 and ALK-6 also coimmunoprecipitate with the truncated type IIA receptor, whereas ALK-3 and ALK-5 do not. Furthermore, the activin type IIB2 receptor does not coimmunoprecipitate with the truncated type IIA receptor, but decreases activin binding to the truncated type IIA receptor. In double immunoprecipitation experiments with cell lysates from COS cells, in which full-length activin type IIA and type IIB2 receptors were cotransfected, no interaction between these receptors was found. In contrast, homomeric complexes of full-length activin type IIA receptors were detected. These results implicate that truncated activin receptors can interfere with activin signaling by interacting with activin type I receptors. Additionally, truncated activin type IIB2 receptors might also interfere with type IIA receptor signaling by decreasing activin binding to the type IIA receptor and therefore might be more potent in inhibiting activin signal transduction. Furthermore, our data indicate that truncated type IIA receptors can interact with other type I receptors and as such might inhibit signal transduction by type I receptors other than activin type IA and type IB receptors.     

The success of locoregional, low-dose recombinant interleukin-2 therapy in tumor-bearing mice is dependent on the time of rIL-2 administration

The most common chromosomal aberrations in myelodysplastic syndromes (MDS) are complete or partial loss of chromosomes 5 and 7, and trisomy 8. To identify genes important in the pathogenesis of this disease that could be associated with these gross chromosomal defects, we have employed the differential display PCR (DDPCR) procedure developed by Liang and Pardee. This method allows simultaneous comparison of several cDNA sources for the presence of differentially expressed genes. Polymorphonuclear cells (PMNs) from two MDS patients, containing a 5q deletion or a trisomy 8, and three healthy controls were used. Initial screening resulted in the identification of five and three partial cDNA sequences, respectively that were either differentially expressed in both patient samples or in individual patients, as compared with the controls. The authenticity of aberrant expression was verified by reanalyzing the same primer combinations on newly prepared cDNA. Differential expression of the three remaining fragments was subsequently checked on a larger panel of MDS patients, using amplicon-specific primer sets. These were obtained by cloning and sequencing of the fragments. For one partial cDNA (DC3), the original expression pattern, i.e., decreased expression in individual MDS patients, was confirmed. These results demonstrate the utility of the DDPCR procedure to isolate differentially expressed sequences in primary patient samples where the availability of cells is a limiting factor.     

Diuretics: role of sodium balance

Diuretics are commonly prescribed for a wide variety of clinical problems, including hypertension, extracellular volume excess, and disorders of calcium metabolism. Although natriuresis with altered sodium balance is not always the therapeutic goal, this feature of the diuretics is essential for optimal results, irrespective of the clinical problem.     

Rapid plasma clearance and reduced rate and extent of urinary elimination of parenterally administered methotrexate as a result of severe vomiting and diarrhoea

A patient received 200 mg methotrexate IM as part of a treatment schedule for malignant melanoma. Severe vomiting and diarrhoea began shortly after treatment and persisted for 4 h. During this period the methotrexate renal clearance rate was 37 ml . min-1, increasing to 97 ml . min-1 when vomiting and diarrhoea ceased. Only 26% of the administered dose was recovered in the urine up to 48 h after treatment, whilst the plasma clearance of methotrexate assessed over the same period was 208 ml . min-1. We conclude that a considerable proportion of the dose was lost from the gastrointestinal tract during the period of vomiting and diarrhoea, and that consequently enterohepatic circulation of methotrexate plays an important role in the pharmacokinetics of the drug.     

Microbenthic chamber with microelectrode for in-situ determination of fluxes of dissolved S(-II), I-, O2, Mn, and Fe

A 2-mL microbenthic chamber was fitted with a microelectrode for the in-situ determination of benthic fluxes of S(-II), I-, O2, Mn(II), and Fe(I). Detection was by voltammetry using a battery operated potentiostat and a gold microelectrode. The chamber was fitted on a Perspex plate to be placed on sediments. Because of the small chamber volume, benthic fluxes could be determined in a few hours rather than days, without the need for sample extraction. Tests on homogenized sediments in the laboratory showed fluxes of 17.1+/-1.8 nmoles cm(-2) min(-1) S(-II) and 1.3+/-0.2 nmoles cm(-2) min(-1) Mn. Benthic fluxes of oxygen and iodide were determined in situ in the field. The oxygen flux was negative (consumption) at a rate of -4.9+/-0.5 nmoles cm(-2) min(-1) O2. The I- flux was initially negative in oxygenated waters at a rate of -30+/-3 pmoles cm(-2) min(-1) and subsequently turned positive to a rate of 12+/-1 pmoles cm(-2) min(-1) when the oxygen concentration dropped. The rate of change in the microbenthic chamber was sufficiently quick to complete a flux measurement within minutes.     

Quantification of model uncertainty from data

Identification of linear models in view of robust control design requires the identification of a control-relevant nominal model, and a quantification of model uncertainty. In this paper a procedure is presented to quantify the model uncertainty of any prespecified nominal model, from a sequence of measurement data of input and output signals from a plant. By employing a nonparametric empirical transfer function estimate (ETFE), we are able to split the model uncertainty into three parts: the inherent uncertainty in the data due to data imperfections, the unmodelled dynamics in the nominal model, and the uncertainty due to interpolation. A frequency-dependent hard error bound is constructed, and results are given for tightening the bound through appropriate input design.     

Initial operation of a pulse-burst laser system for high-repetition-rate Thomson scattering

A pulse-burst laser has been installed for Thomson scattering measurements on the Madison Symmetric Torus reversed-field pinch. The laser design is a master-oscillator power-amplifier. The master oscillator is a commercial Nd:YVO(4) laser (1064 nm) which is capable of Q-switching at frequencies between 5 and 250 kHz. Four Nd:YAG (yttrium aluminum garnet) amplifier stages are in place to amplify the Nd:YVO(4) emission. Single pulses through the Nd:YAG amplifier stages gives energies up to 1.5 J and the gain for each stage has been measured. Repetitive pulsing at 10 kHz has also been performed for 2 ms bursts, giving average pulse energies of 0.53 J with ΔE/E of 4.6%, where ΔE is the standard deviation between pulses. The next step will be to add one of two Nd:glass (silicate) amplifier stages to produce final pulse energies of 1-2 J for bursts up to 250 kHz.     

Detection and Localization of Delaminations in Thin Carbon Fiber Reinforced Composites with the Ultrasonic Polar Scan

In this paper, the hybrid compliance-stiffness matrix method for simulating wave propagation in (delaminated) multilayered media with viscoelastic anisotropy has been confronted with high-quality amplitude and phase experiments on delaminated composites, obtained using the ultrasonic polar scan setup (UPS) in transmission by considering harmonic as well as pulsed ultrasound. Results are presented for multiple thin carbon/epoxy laminates with an artificial edge delamination induced by a foil insert, showing a good agreement between experimental recording and numerical modeling. The obtained results further reveal the feasibility of the harmonic UPS to detect and even locate the depth-position of multiple delaminations in fiber reinforced composites. Considering that the harmonic UPS method does not rely on the detection of different echoes like the classical C-scan, but rather expounds the conditions for efficient stimulation of guided waves in the solid, the method is found to be highly suited for inspecting thin composite materials for the presence of delaminations.     

Tensile and compressive properties of flax fibres for natural fibre reinforced composites

Mechanical properties of standard decorticated and hand isolated flax bast fibres were determined in tension as well as in compression. The tensile strength of technical fibre bundles was found to depend strongly on the clamping length. The tensile strength of elementary flax fibres was found to range between 1500 MPa and 1800 MPa, depending on the isolation procedure. The compressive strength of elementary flax fibres as measured with a loop test lies around 1200 MPa. However, the compressive strength can be lowered severely by the decortication process. The standard decortication process induces kink bands in the fibres. These kink bands are found to contain cracks bridged by microfibrils. The failure behaviour of elementary flax fibres under compression can be described as similar to the failure behaviour of a stranded wire.