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The production of fireproof SiO2/Al2O3 ceramic fibres started in the late forties. Primarily, the production was designed entirely for the aircraft industry. In the sixties the application of ceramic fibres became more wider. The first ceramic fibrous materials were characterised by thermal resistance reaching 1200 degrees C. Certain kinds of materials produced currently can be used in the temperature accounting for 1600 degrees C. Aluminosiliceous ceramic fibres recrystallise at high temperature (above 1000 degrees C) and produce mullite and crostobalite. Ceramic fibrous material may become hazardous to workers as a source of respirable fibres. Studies, carried out in plants which manufacture products from aluminosiliceous ceramic fibres, indicated that mean concentrations of respirable fibres ranged from 0.14 to 1.13 f/cm3 while the levels of mean concentrations of total dust accounted for 0.4-13.6 mg/m3. At working posts of plants producing china, where heat-insulating materials were changed mean level of respirable fibre concentration was 0.28-1.65 f/cm3 and concentration of total dust ranged from 7.0 to 17.7 mg/m3.
Inner ear hair cells have been suggested as attractors for growing afferent fibers, possibly through the release of the neurotrophin brain-derived neurotrophic factor (BDNF). Atoh1 null mice never fully differentiate hair cells and supporting cells and, therefore, may show aberrations in the growth and/or retention of their innervation. We investigated the distribution of cells positive for Atoh1- or Bdnf-mediated beta-galactosidase expression in Atoh1 null and Atoh1 heterozygotic mice and correlated the distribution of these cells with their innervation. Embryonic day (E) 18.5 Atoh1 null and heterozygotic littermates show Atoh1- and BDNF-beta-galactosidase-positive cells in comparable distributions in the canal cristae and the cochlea apex. Atoh1-beta-galactosidase-positive but only occasional Bdnf-beta-galactosidase-positive cells are found in the utricle, saccule, and cochlea base of Atoh1 null mutant mice. Absence of Bdnf-beta-galactosidase expression in the utricle and saccule of Atoh1 null mice is first noted at E12.5, a time when Atoh1-beta-galactosidase expression is also first detected in these epithelia. These data suggest that expression of Bdnf is dependent on ATOH1 protein in some but does not require ATOH1 protein in other inner ear cells. Overall, the undifferentiated Atoh1- and Bdnf-beta-galactosidase-positive cells show a distribution reminiscent of that in the six sensory epithelia in control mice, suggesting that ear patterning processes can form discrete patches of Atoh1 and Bdnf expression in the absence of ATOH1 protein. The almost normal growth of afferent and efferent fibers in younger embryos suggests that neither fully differentiated hair cells nor BDNF are necessary for the initial targeted growth of fibers. E18.5 Atoh1 null mice have many afferent fibers to the apex of the cochlea, the anterior and the posterior crista, all areas with numerous Bdnf-beta-galactosidase-positive cells. Few fibers remain to the saccule, utricle, and the base of the cochlea, all areas with few or no Bdnf-beta-galactosidase-positive cells. Thus, retention of fibers is possible with BDNF, even in the absence of differentiated hair cells.
Fiber-reinforced composites (FRCs) show great promise as long-term restorative materials in dentistry and medicine. Recent evidence indicates that these materials degrade in vivo, but the mechanisms are unclear. The objective of this study was to investigate mechanisms of deterioration of glass fiber-polymer matrix bond strengths in dental fiber-reinforced composites during hydrothermal and mechanical aging. Conventional three-point bending tests on dental FRCs were used to assess flexural strengths and moduli. Micro push-out tests were used to measure glass fiber-polymer matrix bond strengths, and nanoindentation tests were used to determine the modulus of elasticity of fiber and polymer matrix phases separately. Bar-shaped specimens of FRCs (EverStick, StickTech, and Vectris Pontic, Ivoclar-Vivadent) were either stored at room temperature, in water (37 and 100 degrees C) or subjected to ageing (10(6) cycles, load: 49 N), then tested by three-point bending. Thin slices were prepared for micro push-out and nanoindentation tests. The ultimate flexural strengths of both FRCs were significantly reduced after aging (p < 0.05). Both water storage and mechanical loading reduced the interfacial bond strengths of glass fibers to polymer matrices. Nanoindentation tests revealed a slight reduction in the elastic modulus of the EverStick and Vectris Pontic polymer matrix after water storage. Mechanical properties of FRC materials degrade primarily by a loss of interfacial bond strength between the glass and resin phases. This degradation is detectable by micro push-out and nanoindentation methods.
BACKGROUND AND OBJECTIVES: The high-power Thulium fiber laser has previously been shown to rapidly vaporize and coagulate soft urinary tissues (e.g., prostate). This is the first preliminary study of a high-power Thulium fiber laser for fragmentation of urinary stones. STUDY DESIGN/MATERIALS AND METHODS: A continuous-wave, high-power Thulium fiber laser operating at a wavelength of 1.94 microm, was modulated to operate in pulsed mode with an output pulse energy of 1 J through a 300-microm-core silica fiber at a 20 milliseconds pulse length and repetition rate of 10 Hz. The fragmentation time to reduce uric acid (UA) (n = 13) and calcium oxalate monohydrate (COM) (n = 6) stones into particles < 2 mm was measured. RESULTS: Mean initial mass of the UA and COM stones measured 860+/-211 and 763 +/- 204 mg. Fragmentation rates measured 388 +/- 49 and 25 +/- 2 mg/minute. Average time needed to fragment the UA and COM stones into particles < 2 mm was 2.25 +/- 0.63 and 30.7 +/- 8.4 minutes, respectively. CONCLUSIONS: The high-power Thulium fiber laser, when operated in pulsed mode, is capable of fragmenting both soft (UA) and hard (COM) urinary stones. The Thulium fiber laser may be useful as a single laser system for use in multiple soft and hard tissue laser ablation applications in urology.
The signaling pathways linking receptor activation to actin stress fiber rearrangements during growth factor-induced cell shape change are still to be determined. Recently our laboratory demonstrated the involvement of p70 S6 kinase (p70(s6k)) activation in thrombin-induced stress fiber formation in Swiss 3T3 cells. The present work shows that thrombin-induced p70(s6k) activation is inhibited by the PI 3-kinase inhibitors wortmannin and LY-294002. These inhibitors also significantly reduced thrombin-induced stress fiber formation, demonstrating a role for PI 3-kinase activity in this process, most likely upstream of p70(s6k). Furthermore, the p110alpha form of PI 3-kinase was localized to actin stress fibers, as was previously shown for p70(s6k), as well as to a golgi-like distribution. In contrast, PI 3-kinase p110gamma colocalized with microtubules. The PI 3-kinase p85 subunit, known to be capable of association with p110alpha, was present in a predominantly golgi-like distribution with no presence on actin filaments, suggesting the existence of distinctly localized PI 3-kinase pools. Immunodepletion of p85 from cell lysates resulted in only partial depletion of p110alpha and p110alpha-associated PI 3-kinase activity, confirming the presence of a p85-free p110alpha pool located on the actin stress fibers. Our data, therefore, point to the importance of subcellular localization of PI 3-kinase in signal transduction and to a novel action of p85 subunit-independent PI 3-kinase p110alpha in the stimulation by thrombin of p70(s6k) activation and actin stress fiber formation.
We present here the nucleotide sequence of the tail fiber genes of phage 186. Marker rescue was used to associate an open reading frame (ORF) of 462 codons with the previously known tail gene K. A downstream ORF, encoding a 166-amino-acid product, was designated orf 45. Comparative studies suggested that K encodes the tail fiber protein and that orf 45 encodes an assembly protein. K protein contains a succession of short amino acid sequences (motifs) that are homologous with sequences from the tail fiber proteins of unrelated bacteriophages. The fact that these sequence motifs are variously present in the tail fiber proteins of unrelated bacteriophages has been advanced as evidence for horizontal transfer in the evolution of the associated tail fiber genes. However, the fact that the order of the various motifs in the proteins is invariant emphasizes the probability that independent divergence from a common ancestor also played a major role in the evolution of the tail fiber genes.
Adult rabbit zonular fibers maintained in their native condition were treated with collagenase, alpha-chymotrypsin and hyaluronidase, and were observed with the electron microscope. The results obtained were as follows: 1. Collagenase digested the lens capsule, but not the zonular fibers. 2. Long time collagenase action obscured the cell membrane of the lens epithelium and the basal lamina of the ciliary epithelium. 3. Washing with 0.9% NaCl increased the collagenase action on the lens capsule. 4. Alpha-chymotrypsin digested the zonular fibers and the zonular lemalla, but not the lens capsule and the basal lamina of the ciliary epithelium. 5, Hyaluronidase only slightly changed the lens capsule. 6. The vitreous fibers were digested by collagenase, but not by alpha-chymotrypsin or hyaluronidase. Thes results together with the review of recent literature indicate that the zonular fiber has a nature close to that of the microfibril of elastic fiber.
A microfluorometric (MF) technique was developed and validated as a first step in quantifying the growth of sympathohippocampal fibers. This MF technique measures independent components of areal density and fiber intensity. Areal density refers to a basic stereological measure of percentage surface or volume of fluorescent fibers. Fiber intensity refers to the amount of fluorescence (normalized for fading) emitted by varicosities or fibers at a specific wavelength. The first phase of this research was undertaken to identify the criteria yielding the best correlations with the results of classical stereological methods. The second phase then demonstrated that the MF procedure was insensitive to shifts in the use of different criteria. Five areas of the hippocampus, and the pineal and habenula, were measured in 55 animals whose survival times after septal lesions varied widely. With 309 areas finally measured, the strongest intercorrelations separated intensity from density variables. Error variance contributed little to the final solution. We concluded that this MF method was a simple and specific way to measure density and intensity of fluorescent fibers and varicosities. Slight variations in equipment characteristics or in the use of criteria across several laboratories should not affect the results obtained with this method.
Cotton (Gossypium hirsutum L.) fibers are derived from ovule epidermis, which are developmentally similar to Arabidopsis trichome where several MYB transcription factors have been shown to control their formation. However, little is known about the molecular control of cotton fiber initiation. Here we isolated 55 cotton MYB domain-containing sequences expressed in ovules during fiber initiation. Among them, GhMYB109, encoding a R2R3 MYB transcription factor of 234 amino acids, was found to be structurally related to AtMYBGL1 and AtWER controlling the trichome initiation in Arabidopsis thaliana. Southern blot hybridization revealed that GhMYB109 is present as a unique-copy gene in cotton genome. RNA expression analysis showed that it is specifically expressed in cotton fiber initial cells as well as elongating fibers. These results suggested that GhMYB109 likely plays a direct role in the initiation and elongation of cotton fiber cells.
A sequential model for nucleated protein fiber formation is proposed that is similar in broad outline to models proposed previously (Thermodynamics of the Polymerization of Protein, Academic Press, New York, (1975); Biophys. J. 50 (1986) 583) but generalized to allow for thermodynamic nonideality resulting from a high degree of volume occupancy by inert macromolecular cosolutes (macromolecular crowding). The effect of volume occupancy on the rate of fiber formation is studied in the transition-state rate-limited regime through systematic variation of rate-limiting step (prenuclear oligomer formation, nucleus formation or fiber growth), shape of prenuclear oligomer, size of nucleus, extent of reversibility, nature of inert cosolute (hard globular particle or random coil polymer) and size of inert cosolute relative to that of fiber-forming protein. It is found that crowding can accelerate the rate of fiber formation by as much as several orders of magnitude. The extent of acceleration for a given degree of volume occupancy depends upon several factors, the most conspicuous of which is the stoichiometry of the nucleus. In contrast, the rate of redistribution of fiber length, which occurs on a much slower time scale than polymer formation, is found to be insensitive to the extent of crowding.
OBJECTIVE: The aim of this study was to characterize the linear polymerization shrinkage strain of glass fiber-reinforced composite (FRC) according to the fiber orientation. METHODS: Test specimens (n=5) (10.0 x 10.0 x 1.5mm) were prepared from different brands of photopolymerizable resin-preimpregnated FRC; unidirectional continuous FRC, experimental random-oriented FRC, and bidirectional continuous FRC. As control materials, particulate filler composite resin and unfilled dimethacrylate monomer resin were used. Two uniaxial strain gages (gage length 2mm) were used to measure shrinkage strains in two directions: longitudinally and transversally to the fiber direction. The uncured composite or resin was placed on top of the strain gages, covered with a separating sheet and a glass plate, and irradiated for 40s with a light-curing unit. The shrinkage strain was monitored for 300 s. ANOVA and Tukey's posthoc test were used at a significance level of 0.05. RESULTS: ANOVA revealed that orientation of fiber and brand of material had a significant effect (P<0.05) on shrinkage strain. The unidirectional FRC revealed no shrinkage longitudinally to the fiber direction, whereas the shrinkage occurred transversally to the fiber direction. Particulate filler composite resin and unfilled resin revealed equal shrinkage strain in both of the measured directions. SIGNIFICANCE: Anisotropic nature of FRC exists with regard to polymerization shrinkage strain. The variation of polymerization shrinkage strains of FRC compared to those of particulate filler composites and unfilled resin might be important for future clinical applications.
Chemically skinned rabbit psoas muscle fibers/bundles were osmotically compressed with a macromolecule dextran T-500 (0-16%, g/100 ml) at 20 degrees C, 200 mM ionic strength, and pH 7.0. The lattice spacing of psoas bundles was measured by equatorial x-ray diffraction studies during relaxation and after rigor induction, and the results were compared with the fiber width measurements by optical microscopy. The purpose of the present study is to determine whether fiber width is a reliable measure of the lattice spacing, and to determine the available spacing for myosin cross-bridges between the thick and thin filaments. We observed that both the lattice spacing and the fiber width decreased with an increase in the dextran concentration during relaxation or after rigor induction, and that the spacing and the fiber width were proportionately related. We further observed that, in the absence of dextran, the lattice spacing (and the fiber width) shrank on a relax-to-rigor transition, whereas in the presence of 16% dextran, the spacing expanded on a relax-to-rigor transition. The cross-over of these plots occurred at the 4-7% dextran concentration. During Ca activation, the fiber width shrank in the absence of dextran, and it slightly expanded in the presence of 14.4% dextran. The degree of expansion was not as large as in the relax-to-rigor transition, and the cross-over occurred at about 11% dextran concentration. We also carried out experiments with dextran T-40 and T-10 to determine the upper limit of the molecular weight that enters the lattice space. We found that the upper limit is about 20 kD.
Previous work from this laboratory has shown that in cataractous lens from rats fed a 50% galactose diet up to 32 days, synthesis of crystallin mRNAs was reduced while synthesis of mRNAs for the non-crystallin proteins appeared to be maintained at equivalent or higher levels than found in the controls. In this study, we find that the population of mRNA from the 45-day cataractous lens included all of the crystallin mRNAs and substantial amounts of mRNAs for the non-crystallin proteins, in particular those proteins of molecular weights ranging from 45,000 to 92,000, and pIs from 5.5 to 7.0. At the 45-day cataractous stage, the observed mRNA products totaled between 100 and 120, while for the control they numbered between 40 and 50. In addition, hybrid-select measurements with a lambda gt11 MP26 clone established that MP26 mRNA persisted in the fiber cells of 11-, 20-, 32- and 45-day galactosemic lens. The data, therefore, suggest that continuous exposure of the lens to galactose apparently leads to significant fluctuations in mRNA synthesis and survival. Indirect immunofluorescence (with a monospecific polyclonal rabbit anti-MP26 antibody) and light-microscopy studies demonstrated that although the cortical fiber cells were swollen and structurally disoriented, they retained their nuclei, while the enucleated fiber cells were absent. The microscopy data also suggest that differentiation of the epithelial cells to fiber cells continued in the cataractous lens. Fiber-cell migration was backward as compared with the control, and the surviving cells were localized within the cortex and appeared to be surrounded by damaged cells or cell debris. It is suggested that persistent fiber-cell survival, and continued synthesis of various classes of mRNA by the nucleated cells in the cataractous lens could explain why reversal of cataracts results in recovery in both cell morphology and transparency in the non-nuclear portion of the lens.
In this work, the Ni-P coating on carbon fiber surfaces was carried out in order to improve the impact resistance of carbon fibers-reinforced epoxy matrix composites. The fiber surfaces and the fracture behaviors of composites were measured in terms of X-ray diffraction spectrometry (XRD), X-ray photoelectron spectrometry (XPS), scanning electron microscopy (SEM), and falling weight impact testing. From the XRD and XPS measurements, it was observed that Ni-P coating of carbon fibers led to an increase in two phases, i.e., microcrystalline and amorphous, mainly due to the increase of NiP(2), Ni(3)P, and Ni metal. Energy adsorbed by composites through the various fracture mechanisms was seen to be the characteristic distinguishing between nontreated and treated fiber-reinforced composite systems. The Ni-P alloy technique to improve the impact resistance of the composites was shown to be the modification of fiber-epoxy resin interfaces.
The current work incorporates a microscopic study of the effect of fiber orientation on the fiber wetting process and flow of liquid droplets along filter fibers when subjected to airflow and gravity forces. Glass filter fibers in various combinations were oriented at various angles within a plane defined by the airflow direction and were supplied with distilled water in aerosol form. The behavior and flow of the liquid collected by the fibers were observed and measured using a specially developed microscope cell, detailed in the paper. The experimental results were compared to a theoretical model developed to describe the behavior. The theory and experimental results showed good agreement. The developed theory allows an optimum angle to be determined for the internal filter fiber structure in the design of wet filters. A sensitivity analysis of the model was conducted to determine the most important parameters. This will aid design of wet filtration systems such that maximal self-cleaning can be accomplished with minimal water use.
Muscle biopsies from 14 patients with facioscapulohumeral muscular dystrophy (FSHD) aged from 5 to 45 years were studied histochemically with fiber type analysis, focusing on small angular fibers (SAF) to clarify their significance. There were no duration-related or age-dependent histopathological differences between child and adult patients. Variations in fiber size and SAF were observed in all, myonecrosis with occasional phagocytosis in 10 and regenerating fibers in 12 biopsies. Cellular responses including inflammatory cell infiltration (7 biopsies) and connective tissue proliferation (8 biopsies), and fiber architectural changes (9 biopsies) were additional common findings. Although SAF are also commonly seen in patients with Kugelberg-Welander disease and amyotrophic lateral sclerosis, in FSHD they were mostly type 2C fibers which frequently exhibit alkaline phosphatase-positive activity. Therefore SAF in FSHD are mostly the products of a regeneration rather than denervation process.