Pressure-dependent Sellmeier coefficients and material dispersionsfor silica fiber glass

The pressure-dependent Sellmeier coefficients are essential to characterize the optical design parameters for the optical fiber communication systems under deep sea environmental conditions. These coefficients are calculated for densified silica glass for the first time to compute the pressure dependence of material dispersion at any wavelength from the ultraviolet (UV) to 1.71 μm. The zero dispersion wavelength λ₀ (1.2725 μm at 0.1 10⁶ N m ^-2) varies linearly with pressure, and dλ₀/dP is 0.0027 nm/(10⁶ N m^-2). The calculated value is approximately one-third of the experimental value of 0.0076 nm/(10⁶ N m^-2) for a germanium-doped dispersion shifted fiber having λ₀=1.5484 μm and -0.0070 nm/(10⁶ N m^-2) for a pure silica-core fiber cable having λ₀ =1.2860 μm. Since, the refractive indexes are increased with pressure, the negative value of shift of the zero-dispersion wavelength is erroneous. The explanations are due to Ge-doping in silica glass, a possible temperature fluctuation of 0.16°C in the pressure-dependent measurement system of the zero dispersion wavelength and different experimental conditions of the silica glass and the optical fibers. This anomaly can also be attributed to the internal strain development at the core-cladding and fiber-jacketing boundaries due to pressure, which shows a larger experimental value. It accounts for the experimental values satisfactorily     

Immobilization of N-carbamyl-D-amino acid amidohydrolase

N-Carbamyl-D-amino acid amidohydrolase (DCase), produced with recombinant Escherichia coli cells using a cloned gene from Agrobacterium sp. strain KNK712, has been immobilized for use in the production of D-amino acids. The porous polymers, Duolite A-568 and Chitopearl 3003, were much better than other resins for the activity and stability of the adsorbed enzyme. The activity of DCase expressed on Duolite A-568 and Chitopearl 3003 amounted to 96 units/g-wet-resin and 91 units/g-wet-resin, respectively. DCase immobilized on Duolite A-568 was found to be most stable at about pH 7, and it was further stabilized by reductants such as dithiothreitol, L-cysteine, cysteamine, and sodium hydrosulfite. The stability during the repeated batch reactions was greatly improved when dithiothreitol was in the reaction mixture, and the higher crosslinking degree with glutaraldehyde also stabilized the immobilized enzyme. After 14 times repeated reactions, the remaining activity of the immobilized enzyme cross-linked with 0.1% and 0.2% of glutaraldehyde, and 0.2% of glutaraldehyde with dithiothreitol in the reaction mixture was 12%, 18%, and 63%, respectively. DCase produced with Pseudomonas sp. strain KNK003A and Pseudomonas sp. strain KNK505, which are thermotolerant soil bacteria, and that with Agrobacterium sp. strain KNK712 were also immobilized on Duolite A-568. The stability of the enzymes of thermotolerant bacteria during reactions was superior to that of Agrobacterium sp. strain KNK712, though the activity was lower than that of strain KNK712.     

Effects of a neutral endopeptidase inhibitor, BP102, on the development of deoxycorticosterone acetate-salt hypertension in kininogen-deficient Brown Norway Katholiek rats

The nature of all of the peptides critical to the mechanism(s) of the antihypertensive action of neutral endopeptidase (NEP) inhibitors is still unclear, but bradykinin is thought to be one such peptide. This study was designed to assess the effectiveness of an NEP inhibitor in deoxycorticosterone acetate (DOCA)-salt treated kininogen-deficient Brown Norway Katholiek (BN-Ka) rats. Oral administration of BP102 (10-100 mg/kg), an NEP inhibitor, increased urine volume and urinary sodium excretion in a dose-dependent manner in anesthetized Sprague-Dawley rats. DOCA-salt hypertension was induced in both BN-Ka and Brown Norway Kitasato (BN-Ki) rats after left nephrectomy. The development of DOCA-salt hypertension in normal BN-Ki rats was prevented, and that in BN-Ka rats was also significantly reduced, by an 8-day administration of BP102. When BP102 was administered for 5 weeks, the high blood pressure of DOCA-salt treated BN-Ka rats was markedly lowered, and their heart weights were reduced. These results suggest that kinins play no role in the antihypertensive effect of this inhibitor and that other factors may be involved in this effect.     

Macrophages in normal cycling human ovaries; immunohistochemical localization and characterization

We evaluated the immunolocalization and characterization of macrophages in 28 normal cycling human ovaries. Two primary antibodies were used to detect the macrophages: PGM1, a general marker for macrophages, and 25F9 which is specific for phagocytosing macrophages. Spindle-shaped cells positive for PGM1 but negative for 25F9 were observed in the stroma (123.6 +/- 1.05 cells/10(-6) m2) and theca layer of the follicle (mean ranged from 22.61 to 53.79) and the number of these cells did not change throughout the cycle. After ovulation, PGM1 positive cells with ballooning bodies began to appear in the early corpus luteum (111.8 +/- 0.83). The number of these macrophages increased in the mid and late corpora lutea, and reached maximum in the early degenerating corpus luteum (1231.0 +/- 3.29). A lower number of PGM1 positive ballooning macrophages were observed in the atretic follicle (177.9 +/- 1.42). 25F9 positive cells were also observed among the PGM1 positive balloon-shaped cells. The number of cells double positive for 25F9 and PGM1 was observed in the mid corpus luteum (44.6 +/- 0.46), increased in the late corpus luteum and early degenerating corpus luteum, and reached plateau in the late degenerating corpus luteum (549.0 +/- 5.82). A lower number of these double positive macrophages were also observed in the atretic follicle (64.8 +/- 0.36). The ratio of 25F9 to PGM1 positive cells increased in parallel with ageing of the corpus luteum (0.19 in the mid corpus luteum, 0.39 in the late corpus luteum, and 0.37 in the early degenerating corpus luteum), and the great majority of PGM1 positive cells were also immunopositive for 25F9 in the late degenerating corpus luteum (0.81). These results suggest that in normal cycling human ovaries, macrophages are mainly involved in luteal regression as scavengers.     

Cyclic changes of vasculature and vascular phenotypes in normal human ovaries

In order to study alterations of angiogenesis and blood vessel regression through ovarian cycle in human ovaries we quantitatively examined vascularity in various stages in 24 normal human ovaries. Vascular density (VD; vessel numbers/10(-7) m2) and endothelial area of each vessel (EA; 10(-12) m2/vessel) were evaluated using immunohistochemistry of CD34 and CAS 200 image analysis system. Small-sized vessels were sporadically observed in stroma adjacent to primordial or primary follicles (6.73 +/- 1.83 for VD and 113.58 +/- 21.80 for EA). Formation of capillary network was observed in the theca layer of preantral follicles (PA; 15.28 +/- 2.77 for VD and 113.58 +/- 21.80 for EA), and higher density of the capillary network was detected in non-dominant follicles in follicular phase (ND-F) and dominant follicles (DF; 29.33 +/- 3.84 for VD and 179.69 +/- 41.25 for EA). Dense capillary network was still present in non-dominant follicles in luteal phase (ND-L) and atretic follicles (AF; 26.88 +/- 3.36 for VD and 110.88 +/- 50.53 for EA). After ovulation, developing capillaries were also observed in the luteinized granulosa layers in early corpus luteum (21.95 +/- 2.06 for VD and 167.08 +/- 29.59 for EA). Vessel density markedly increased in mid corpus luteum, reached plateau in late corpus luteum (60.85 +/- 5.92 for VD and 70.99 +/- 15.57 for EA) and remained constant during degenerating corpora lutea. Vascular endothelial growth factor was immunohistochemically observed in the theca cells in PA, ND-F, DF and ND-L in follicular stages, and functioning corpora lutea. Immunoreactivity of intercellular adhesion molecule-1 was detected only in post-capillary venules in early degenerating corpora lutea. These findings suggest that ovarian angiogenesis is a requirement for the early stages of folliculogenesis and luteal growth, and also plays an important role in the process of follicular atresia and luteal regression.     

Identification of a 100-kb region of common allelic loss on chromosome bands 10q25-q26 in human endometrial cancer

A 10-year-old boy with Henoch-Sch?nlein purpura complicated by encephalopathy, transient cortical blindness, and a secondary generalized seizure is reported. Reversible changes in the posterior white and gray matter were seen on magnetic resonance imaging. Our patient illustrates uncommon neurologic manifestations of Henoch-Sch?nlein purpura. The nature and location of the lesions and the normalization of the patient's magnetic resonance imaging is consistent with a posterior predominant parieto-occipital encephalopathy and suggests that cerebral edema from blood-brain barrier breakdown may play a central role in the pathophysiology of the central nervous system symptomatology in some patients.     

Mass Tansfer Characteristics of a Microchannel Device of Split‐Flow Type

A solute was transferred from an aqueous solution to deionized water in a microchannel device with a rectangular channel of 200 μm × 200 μm. The two liquid layers flowed in parallel within the rectangular channel. After making contact in the channel, the layers were split into two streams through a knife‐edge. The amount of solute transferred was determined by analyzing liquid samples taken from the outlet. Thus, conventional analytical instruments were readily available for obtaining the total concentration. Mass tansfer characteristics were examined through the measurement of diffusion coefficients for several solutes. Although the two liquids were carefully supplied at the same velocity, equal flow splitting was difficult to obtain. The unequal splitting led to scattering of the observed solute concentrations at a fixed supply flow rate. This could be a serious drawback as a mass tansfer device; however, a method was proposed to choose an appropriate value for equal splitting. The ratio of effluent flow rate of one liquid to another was changed intentionally. The solute concentration in the receiving liquid for the flow rate ratio of unity corresponds to the data for equal flow splitting. On the basis of the solute concentrations defined, the diffusion of benzoic acid was successfully analyzed using a conventional penetration model with a correction parameter. Furthermore, diffusion coefficients for sucrose and glycine were determined using the basic equation obtained with benzoic acid. The observed values compared fairly well with reported ones. The correction parameter expresses characteristics of the microchannel device; however, the physical picture is still unclear.     

Retroviral vector targeting human cells via c-Kit-stem cell factor interaction

Targeted gene transfer into hematopoietic stem cells by retroviral vectors would greatly facilitate the development of in vivo strategies for stem cell gene therapy. We engineered a recombinant retroviral vector that can target human cells expressing a c-Kit receptor via a ligand-receptor interaction. The ecotropic (Moloney murine leukemia virus) envelope protein was modified by insertion of a sequence encoding the N-terminal 161 amino acids of murine stem cell factor (mSCF), the ligand for murine c-Kit. The chimeric envelope protein was correctly processed and incorporated into viral particles as efficiently as the wild-type envelope protein. Virions pseudotyped with the chimeric envelope proteins bound to 293 cells expressing murine c-Kit (293KIT) preferentially; however, they could not transduce any c-Kit-positive cells under conventional conditions. They could transduce 293KIT cells in the presence of chloroquine, and HEL cells expressing human c-Kit on a fibronectin fragment (CH296)-coated dish. The fact that recombinant mSCF in the medium at the time of transduction greatly reduced the efficiency of both gene deliveries implies that the vector utilized the mSCF-c-Kit interaction for the initial step of transduction in either case. The vector may prove useful for targeting cells expressing c-Kit on their surface.     

Monitoring of Steel Railway Floor Beams Prestressed by Steel Plates

Steel cables and tendons are commonly used in reinforcing steel beams as well as in concrete beams. However, the structural detail of cable anchors in steel beams tends to be complicated, and the effect on reducing live load stresses is not significant because of the relatively small stiffness of cables and tendons. On the contrary, by using high strength steel plates instead of cables and tendons, structural detail of the anchor area becomes simpler, and live load stresses as well as dead load stresses can be reduced in steel beams because of the relatively large stiffness of steel plates. In this study, the steel plate prestressing method is applied to beam specimens and intermediate floor beams of a steel railway through girder bridge. The behavior of the reinforcing steel plates and reinforced steel beams is monitored during prestressing and live loading, in order to assess the effects of prestressing and reinforcement. The study confirmed that these effects are beneficial to the performance of steel railway floor beams.