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- Function and control of fine particles in a living body/
- [Fine Particles] Year Started : 2019
Group Leader
International Center for Materials Nanoarchitectonics(WPI-MANA)
National Institute for Materials Science(NIMS)
Anaerobic microbial activity inside certain biofilms is maintained by the movement of electrons between bacterial cells, referred as “electrical symbiosis”. In this project, I will study the physiological role of redox-active membrane vesicles in oral biofilm causing periodontal disease from the perspective of electrosymbiosis. The electrochemical interaction between membrane vesicles and pathogenic bacteria in the biofilms will be studied by whole-cell electrochemical and mass spectrometry techniques that we have develped. The elucidation of the physiological importace of redox-active membrane vescles would enable us to develop technologies to monitor and control the activity of pathogenic bacteria.
Researcher
Engineering of Tissue Grafts for Hair Regenerative Medicine Project
Kanagawa Institute of Industrial Science and Technology
In this project, I aim to elucidate melanosome transfer in hair follicles by using time-lapse imaging and to identify genes involved in melanosome transfer by microarray analysis.
Associate Professor
Faculty of Pharmacy
Keio University
Microparticles in the air are inhaled into the respiratory tracts and induce immune responses, sometimes cause respiratory diseases. The way of microparticle into the body across the epithelium is largely unknown. We found that M cells are in the airway and have a high uptake capacity of microparticles. In this research project, I will investigate the molecular mechanisms underlying the transcytosis of microparticles by M cells. I will clarify the physical properties of microparticles that are easily incorporated into cells by using in vitro culture model. I will further investigate the differentiation mechanisms of airway M cells. I will generate airway-specific M-cell-null mice to investigate the biological significance of airway M cells in respiratory diseases and allergy.
Associate Professor
Graduate School of Science
Tohoku University
Exosome surfaces vary depending on the cellular origins and the physiological conditions of the cells. This research aims to design new class of exosome-binding fluorescent probes whose signals significantly response to the exosome surfaces with a view toward the development of novel exosome-based diagnostics.
Associate Professor
Graduate School of Medicine
Nagoya University
Viral infection elicits a variety of host cell responses, causing symptoms and diseases. Epstein-Barr virus (EBV), a ubiquitous gamma-herpesvirus, causes various diseases in human, including benign infectious mononucleosis and some malignancies. In this study, I will investigate how exosomes released from EBV-infected cells contribute to disease formation in benign and malignant virus-associated diseases. Therefore, I would like to demonstrate the importance of exosomes in virus-associated diseases.
Assistant professor
Life Science Center for Survival Dynamics
University of Tsukuba
Parasitoid wasps produce a variety of bioactive substances to avoid their host immune system and take nutrition without disturbing their hosts’ development. This project aims to identify the venom components of particles which are produced by parasitoid wasps and examine the functional roles and dynamics of particles as a novel hijack strategy of parasitism. This study provides significant insight into developing environmental-friendly insecticides or antibiotics against pathogenic fungi.
Associate Professor
Graduate School of Engineering
Osaka Prefecture University
A novel micro and nanofluidic device for size classification of exosomes will be developed. After the size classification of exosomes obtained from cultured cells, aptamers specifically binding with exosomes will be selected by a newly developed microdevice based on electrophoretic filtration. Aptamer tags which are degitalized sequences of exosome aptamers, will be analyzed by deep learning for orign descrimination and body kinetics analysis of exosomes.
Lecturer
College of Engineering
Shizuoka University
Bacteria secrete extracellular vesicles called as “membrane vesicles (MVs)”. MVs have roles of transfering virulence factors and signals to other cells. Vesicle formation is enhanced in biofilms, which are bacterial aggregated state, but the mechanism remains unknown. The aim of this study is to understand the molecular mechanism on vesicles secretion of pathogenic bacterium Pseudomonas aeruginosa at the biofilm state. It might provide new insight into vesicle-mediated infection and contribute to the regulation of pathogenesis.
Associate professor
Graduate School of Engineering
Nagoya University
I conduct a nanowire-based comprehensive capture method for extracellular vesicles (EVs) and a machine learning-based miRNA profiling for analysis of “tumor miRNA/tumor secreting EV-miRNA”, “EV-miRNA in blood”, and “EV-miRNA in urine.” And then, I unveil miRNA secretion pathway throuhg categolizing EV-miRNA into four types: cancer-related miRNA, cancer-reacted miRNA, noise miRNA, and unknown miRNA.
Associate Professor
Institute of Medical, Pharmaceutical and Health Sciences
Kanazawa University
The capacity to distinguish self from non-self is a key feature of the immune system. Intrathymic selection events that shape the developing T cell repertoire are a critical component of quality control in the immune system. A failure of self-tolerance results in autoimmune tissue-destruction. Antigen-presenting cells (APCs) in the thymus contribute to the selection of developing T cells. However, it remains unknown how the tiny population of thymic APCs could educate a vast repertoire of T cells. I will clarify the contribution of extracellular vesicles (EV) in T cells development. In particular, I will analyze whether thymic EVs could delete autoreactive T cells. As an application, I will develop engineered exosomes, which can regulate immune response against self and non-self.