A Delivery Method for Compound Video Playback in Wireless Network

ISPA2006 : International Symposium on Parallel and Distributed Processing and Applications , Dec 4-7, 2006 , Sorrento, ItalyIn this paper, we propose a method to realize compound video (multiple videos on a layout)delivery service for mobile terminals. In the proposed method, we introduce proxies which receive multiple videos from corresponding servers and produce a composite video from the received videos in real-time according to the layouts which users specify. However, if users require sets of videos with slightly different layouts, multiple similar composite videos will be generated and the wireless bandwidth will be suppressed to transfer them. So, the proposed method identifies the common part in layouts of user requirements, and transmits to each user a composite video corresponding to the common part and remaining videos. We have developed a greedy algorithm which calculates the set of videos to be transmitted within the available bandwidth, so that the sum of satisfaction degrees of all users is maximized. Through experiments, we confirmed that our method can achieve much higher user satisfaction degrees compared to the case that each user terminal receives multiple videos separately and plays them back in parallel

Optimizing Charge Switching in Membrane Lytic Peptides for Endosomal Release of Biomacromolecules.

Endocytic pathways are practical routes for the intracellular delivery of biomacromolecules. Along with this, effective strategies for endosomal cargo release into the cytosol are desired to achieve successful delivery. Focusing on compositional differences between the cell and endosomal membranes and the pH decrease within endosomes, we designed the lipid-sensitive and pH-responsive endosome-lytic peptide HAad. This peptide contains aminoadipic acid (Aad) residues, which serve as a safety catch for preferential permeabilization of endosomal membranes over cell membranes, and His-to-Ala substitutions enhance the endosomolytic activity. The ability of HAad to destabilize endosomal membranes was supported by model studies using large unilamellar vesicles (LUVs) and by increased intracellular delivery of biomacromolecules (including antibodies) into live cells. Cerebral ventricle injection of Cre recombinase with HAad led to Cre/loxP recombination in a mouse model, thus demonstrating potential applicability of HAad in vivo

Severe Hypomyelination and Developmental Defects Are Caused in Mice Lacking Protein Arginine Methyltransferase 1 (PRMT1) in the Central Nervous System

Protein arginine methyltransferase 1 (PRMT1) is involved in cell proliferation, DNA damage response, and transcriptional regulation. While PRMT1 is extensively expressed in the central nervous system (CNS) at embryonic and perinatal stages, the physiological role of PRMT1 was poorly understood. Here, to investigate the primary function of PRMT1 in the CNS, we generated CNS-specific PRMT1 knockout mice by Cre-loxP system. These mice exhibited post-natal growth retardation with tremors and most of them died in two weeks after birth. Brain histological analyses revealed the prominent cell reduction in the white matter tracts of the mutant mice. Furthermore, ultrastructural analysis demonstrated that myelin sheath was almost completely ablated in the CNS of these animals. In agreement with hypomyelination, we also observed that most major myelin proteins including MBP, CNPase, and MAG were dramatically decreased, although neuronal and astrocytic markers were preserved in the brain of CNS-specific PRMT1 knockout mice. These animals had reduced number of OLIG2+ oligodendrocyte lineage cells in the white matter. We found that expressions of transcription factors essential for oligodendrocyte specification and further maturation were significantly suppressed in the brain of the mutant mice. Our findings provide evidence that PRMT1 is required for CNS development, especially for oligodendrocyte maturation processes

AQT-D: Demonstration of the Water Resistojet Propulsion System by the ISS-Deployed CubeSat

AQT-D (AQua Thruster-Demonstrator) is a 3U CubeSat for a demonstration of a water resistojet propulsion system developed by The University of Tokyo. AQT-D installed the 1U propulsion system using water as a propellant, named AQUARIUS-1U (AQUA ResIstojet propUlsion System 1U). We completed the design and assembly of the AQT-D flight model. AQUARIUS-1U was fired on a pendulum-type thrust balance, and its performance was directly characterized in both a stand-alone test and an integrated test using an entire spacecraft system. AQT-D is currently scheduled to be delivered to JAXA in July 2019 and launched to the International Space Station (ISS) in the middle of 2019 by the H-IIB rocket. AQT-D will be deployed from the Japanese Experiment Module (JEM), known as Kibo, and demonstrate water propulsion technology

A Clinico-pathological Study of Gastric Polyps Treated with Endoscopic Polypestomy

181 gastric polyps obtained by endoscopic polypectomy were studied clinico-pathologically. The polyps occurred most frequently in the lower portion, and the incidence of the polyps tended to increase with age. 91% (164/181) of the polyps were occupied by hyperplastic polyps, and 3 polyps and one polyp respectively with dysplastic and carcinomatous foci were detected in 164 hyperplastic polyps. Although hyperplastic polyps rarely transform into dysplasia or carcinoma, careful follow-up is recommended