Factors regulating SCC antigen expression in squamous cell carcinoma of the uterine cervix

Expression of squamous cell carcinoma (SCC) antigen emerged concurrently with squamous formation of the uterine cervix and increased during the neoplastic transformation of the cervical squamous epithelium. SCC antigen expression differed considerably among the histomorphologic cell types of cervical carcinoma. Large cell nonkeratinizing carcinoma contained high levels of the antigen. In contrast, no appreciable expression of SCC antigen was observed in small cell nonkeratinizing carcinoma. The pattern of SCC antigen expression closely coincided with EGF receptor (EGF-R) expression in cervical squamous neoplasia. This suggests that the expression of SCC and EGF-R in cervical carcinoma is related to the differentiation or dedifferentiation processes of the tumor cells. SCC production by CaSki cervical epidermoid carcinoma cells was stimulated by EGF. It seems likely that an autocrine system, in which EGF serves as the signal, may exist in cervical squamous carcinoma. 17beta-estradiol and L-triiodothyronine were found to upregulate EGF-R expression, proliferative potential and SCC production in the CaSki cervical carcinoma cells.     

Noninvasive blood glucose assay using a newly developed near-infrared system

This paper reports in vivo near-infrared (NIR) noninvasive blood glucose assay using dermis tissue spectra. We assume that the glucose content in dermis tissue traces the variations in blood glucose. For dermis spectra measurements, epidermis, especially stratum corneum, acts as an interference in skin tissue. Thus, we have developed a method for the selective measurement of dermis tissue spectra, enabling us to obtain better quality spectra for an accurate blood glucose assay. The selective measurement of the dermis spectra realized by using a newly developed fiber-optic probe that consists of source and detector optical fibers separated by 0.65 mm on a skin surface. The light path in the skin tissue for this geometry has been simulated by a Monte Carlo method. The simulation results show that detected light mainly interrogates dermis tissue. As the absorbance signal of glucose in human tissue is extremely small, the quality of the measured spectra is critical for the reliable assay. The present method for blood glucose assay has been applied to one Type 1 diabetic. The correlation coefficient between the blood glucose content predicted by NIR spectra and those measured by finger-prick was 0.928 and the standard error of prediction was 32.2 mg/dL. These results demonstrate the potential of our methodology for noninvasive NIR blood glucose assay.     

Studies on in vitro synthesis and secretion of human chorionic gonadtropin and its subunits

Data from cattle herds infected with brucellosis and from control (noninfected) herds were collected and analyzed using case control techniques. It appeared that herds located close to other infected herds and those herds whose owners made frequent purchases of cattle had an increased risk of acquiring brucellosis, particularly those who made purchases from other herds or from cattle dealers. Infected herds had a lower level of vaccination than noninfected herds. However, the percentage vaccinated was highly variable in each group. Vaccination per se did not appear to adversely influence the interpretation of serological test results nor did it appear to protect the individual animal. Once infected, the time required to become free of brucellosis was increased by large herd size and/or loose housing. Closed herds also took longer to become brucellosis free than more open herds. The percentage of animals removed from the herd was increased by active abortion. Those herds with multiple serological reactors (positives and questionables) at the first herd test after the imposition of quarantine had the highest percentage of cattle removed.     

Clinical evaluation of urinary leukotriene E4 levels in asymptomatic bronchial asthma

To evaluate the significance of peptide leukotrienes (LTC4, D4, E4) in asymptomatic asthmatic patients, we measured urinary LTE4 levels which is thought to reflect in vivo production of peptide LTs. Urinary LTE4, was extracted using C18 solid phase column and measured by radioimmunoassay. There was no significant difference in urinary LTE4 levels among asthmatics with different severity or between atopic and non-atopic asthmatics. Urinary LTE4 levels were significantly elevated in asthmatics compared with normal controls (p < 0.05). When compared with normal controls, urinary LTE4 levels were significantly elevated in moderate to severe asthma (p < 0.05), and non-atopic asthmatics (p < 0.001). Urinary LTE4 levels were significantly elevated in aspirin-sensitive asthmatics compared with aspirin-tolerant asthmatics (p < 0.05). There was no significant difference in urinary LTE4 levels among aspirin-sensitive asthmatics with different severity. These results suggest that increased production of peptide LTs is a characteristic in aspirin-sensitive asthma, and that the severity and type of asthma and the presence of aspirin-sensitive asthma should be taken into consideration in the analysis of urinary LTE4 levels.     

Evanescent-wave holography by use of surface-plasmon resonance

We report a method for evanescent-wave holography using surface-plasmon resonance from the illumination light. The device we have made consists of three layers: a prism of high refractive index, a thin metallic film, and a grating. Evanescent waves generated by the surface plasmons are diffracted with a prerecorded grating to reconstruct a three-dimensional image. The possibility of white-light illumination and the application to a flat display system with waveguides in the proposed method are discussed.     

Resolution enhancement printing with a variable spot-size laser diode

We demonstrate enhanced resolution printing using a variable spot-size laser diode. The near-field spot size of the laser diode can be changed by controlling the refractive-index distribution in the laser stripe through the injected current. The ratio of the minimum-to-maximum spot size is 2.1:1. This technology provides high-resolution printing without increasing the scanning frequency. Smoother character outlines that consist of finer steps are produced with this laser diode. An effective resolution of 1200 dots /in. (dpi) can be obtained by a printer system with 600-dpi resolution.     

Multibeam scanning optics with single laser source for full-color printers

In the novel optical system described here, four-color toners can be developed in one rotation of the photoconductor, and the color control information is given when the intensities of the laser power levels are changed and the two polarization directions are switched. A polarizing beam splitter between the common scanning optics and the photoconductor enables the laser beam to pass through a common scanning system and to illuminate two positions on the photoconductive material. The laser beam polarization direction is controlled by an electro-optical device immediately behind the laser. In each illuminated position, two-color toners are developed by a three-level (trilevel) photographic process. This simplified optical system eliminates the registration errors that occur with four-color information items and can be useful in high-speed printing systems.     

Fully automated two-dimensional electrophoresis system for high-throughput protein analysis

We developed a fully automated electrophoresis system for rapid and highly reproducible protein analysis. All the two-dimensional (2D) electrophoresis procedures including isoelectric focusing (IEF), on-part protein staining, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and in situ protein detection were automatically completed. The system comprised Peltiert devices, high-voltage generating devices, electrodes, and three disposable polymethylmethacrylate (PMMA) parts for IEF, reaction chambers, and SDS-PAGE. Because of miniaturization of the IEF part, rapid IEF was achieved in 30 min. A gel with a tapered edge gel on the SDS-PAGE part realized a connection between the parts without use of a gluing material. A biaxial conveyer was employed for the part relocation, sample introduction, and washing processes to realize a low-maintenance and cost-effective automation system. Performances of the system and a commercial minigel system were compared in terms of detected number, resolution, and reproducibility of the protein spots. The system achieved high-resolution comparable to the minigel system despite shorter focusing time and smaller part dimensions. The resulting reproducibility was better or comparable to the performance of the minigel system. Complete 2D separation was achieved within 1.5 h. The system is practical, portable, and has automation capabilities.