Simple Measurement System for Biological Signal Using a Smartphone

This paper describes simple measurement system for biological signal using smartphone. The proposed system consists of an instrumentation amplifier, a filter and an AC/DC converter. The biological signal is converted to the digital data through the microphone terminal with A/D converter in the smartphone. In many cases, the circuits require the power sources such as the cell batteries, however, the proposed system is supplied the power through the earphone terminal of the smartphone. Therefore, the proposed system no require the batteries. The software of this system parallelizes the processing so that the earphone output and the microphone terminal can be executed at the same time. The proposed system was verified through the measurement of surface electromyogram using discrete parts and iOS. Results of experimentation, the proposed system was operating correctly

New active diode with bulk regulation transistors and its application to integrated voltage rectifier circuit

This paper describes new active diode with bulk regulation transistors and its application to the integrated voltage rectifier circuit for a biological signal measurement system with smartphone. The conventional active diode with BRT has the dead region which causes leak current, and the output voltages of the application (e.g. voltage rectifier circuit) decrease. In order to overcome these problem, we propose new active diode with BRT which uses the control signal from the comparator of active diode to eliminate the dead region. Next we apply the proposed active diode with BRT to the integrated voltage rectifier circuit. The proposed active diode with BRT and voltage rectifier circuit were fabricated using 0.6 μm standard CMOS process. From experimental results, the proposed active diode with BRT eliminates the dead region perfectly, and the proposed voltage rectifier circuit generates + 2.86 V (positive side) and - 2.70 V (negative side) under the condition that the amplitude and frequency of the input sinusoidal signal are 1.5 V and 10 kHz, respectively, and the load resistance is 10 kΩ

A high-resolution fringe printer for studying synthetic holograms

A high resolution fringe printer developed for driving the research in computer-generated holograms is presented. This fringe printer consists of a rotation drum and a laser diode and is capable of printing elliptical dots of 1.5 times 3.0 microns in diameter on photosensitive films. These dot sizes are approximately converted into resolutions of 17,000dpi × 8,500dpi. The horizontal and vertical angles of viewing-zone of holograms printed by the printer reach 24 and 12 degrees, respectively. The designed maximum scan speed is more than 200mm/s, and at current stage of development, a hologram of approximately 50 mm square can be printed in approximately 2 hours

Effect of inactivated Streptococcus pneumoniae as non-pathogenic particles on the severity of pneumonia caused by respiratory syncytial virus infection in mice

The severity of pneumonia in respiratory syncytial virus (RSV) infection is strongly related to hostimmune response and external factors such as bacteria and environmental chemicals. Weinvestigated the effect of inactivated Streptococcus pneumoniae (ISP) as non-pathogenic particleson the severity of pneumonia in RSV-infected mice. Mice were intranasally exposed to ISP beforeRSV infection. On day 5 post-infection, we examined the lung tissues, virus titer, and infiltratedcells in the lungs. The ISP did not cause significant histopathological effects on lungs of RSVinfectedmice and reduced virus titer in the lungs. It reduced the ratio of lymphocyte infiltrationinto the lungs and consequently the ratio of macrophage increased. In addition, we found that ISPincreased RANTES level in bronchoalveolar lavage fluid from RSV-infected mice on day 1 postinfection,but reduced type I interferon levels. Thus, ISP did not exacerbate pneumonia in RSVinfection; rather, it might mildly reduce the severity. We characterize and discuss the inherentactivity of ISP as non-pathogenic particles inducing the role of RANTES on the pneumonia in RSVinfection.九州保健福祉大学201

Cellular response of Parachlorella kessleri to a solid surface culture environment

Attached culture allows high biomass productivity and is a promising biomass cultivating system because neither a huge facility area nor a large volume of culture medium are needed. This study investigates photosynthetic and transcriptomic behaviors in Parachlorella kessleri cells on a solid surface after their transfer from liquid culture to elucidate the physiological and gene-expression regulatory mechanisms that underlie their vigorous proliferation. The chlorophyll content shows a decrease at 12 h after the transfer; however, it has fully recovered at 24 h, suggesting temporary decreases in the amounts of light harvesting complexes. On PAM analysis, it is demonstrated that the effective quantum yield of PSII decreases at 0 h right after the transfer, followed by its recovery in the next 24 h. A similar changing pattern is observed for the photochemical quenching, with the PSII maximum quantum yield remaining at an almost unaltered level. Non-photochemical quenching was increased at both 0 h and 12 h after the transfer. These observations suggest that electron transfer downstream of PSII but not PSII itself is only temporarily damaged in solid-surface cells just after the transfer, with light energy in excess being dissipated as heat for PSII protection. It thus seems that the photosynthetic machinery acclimates to high-light and/or dehydration stresses through its temporal size-down and functional regulation that start right after the transfer. Meanwhile, transcriptomic analysis by RNA-Seq demonstrates temporary upregulation at 12 h after the transfer as to the expression levels of many genes for photosynthesis, amino acid synthesis, general stress response, and ribosomal subunit proteins. These findings suggest that cells transferred to a solid surface become stressed immediately after transfer but can recover their high photosynthetic activity through adaptation of photosynthetic machinery and metabolic flow as well as induction of general stress response mechanisms within 24 h

Odontogenic stem cells

Epithelial cell rests of Malassez (ERM) are quiescent epithelial remnants of the Hertwig’s epithelial root sheath (HERS) that are involved in the formation of tooth roots. ERM cells are unique epithelial cells that remain in periodontal tissues throughout adult life. They have a functional role in the repair/regeneration of cement or enamel. Here, we isolated odontogenic epithelial cells from ERM in the periodontal ligament, and the cells were spontaneously immortalized. Immortalized odontogenic epithelial (iOdE) cells had the ability to form spheroids and expressed stem cell-related genes. Interestingly, iOdE cells underwent osteogenic differentiation, as demonstrated by the mineralization activity in vitro in mineralization-inducing media and formation of calcification foci in iOdE cells transplanted into immunocompromised mice. These findings suggest that a cell population with features similar to stem cells exists in ERM and that this cell population has a differentiation capacity for producing calcifications in a particular microenvironment. In summary, iOdE cells will provide a convenient cell source for tissue engineering and experimental models to investigate tooth growth, differentiation, and tumorigenesis

Down-regulation of GATA1-dependent erythrocyte-related genes in the spleens of mice exposed to a space travel

Secondary lymphoid organs are critical for regulating acquired immune responses. The aim of this study was to characterize the impact of spaceflight on secondary lymphoid organs at the molecular level. We analysed the spleens and lymph nodes from mice flown aboard the International Space Station (ISS) in orbit for 35 days, as part of a Japan Aerospace Exploration Agency mission. During flight, half of the mice were exposed to 1 g by centrifuging in the ISS, to provide information regarding the effect of microgravity and 1 g exposure during spaceflight. Whole-transcript cDNA sequencing (RNA-Seq) analysis of the spleen suggested that erythrocyte-related genes regulated by the transcription factor GATA1 were significantly down-regulated in ISS-flown vs. ground control mice. GATA1 and Tal1 (regulators of erythropoiesis) mRNA expression was consistently reduced by approximately half. These reductions were not completely alleviated by 1 g exposure in the ISS, suggesting that the combined effect of space environments aside from microgravity could down-regulate gene expression in the spleen. Additionally, plasma immunoglobulin concentrations were slightly altered in ISS-flown mice. Overall, our data suggest that spaceflight might disturb the homeostatic gene expression of the spleen through a combination of microgravity and other environmental changes