Structure of Silicene Grown on Ag(111) Single Crystal

学位の種別: 課程博士審査委員会委員 : （主査）東京大学特任教授 川合 眞紀, 東京大学准教授 高木 紀明, 東京大学教授 吉信 淳, 東京大学教授 斉木 幸一郎, 東京大学客員教授 前田 瑞夫University of Tokyo(東京大学

Data supporting the role of Fyn in initiating myelination in the peripheral nervous system

Transgenic mice, which express active Fyn tyrosine kinase under the control of a glial fibrillary acidic protein promoter, have been produced. This promoter induces protein expression in the initiation stage of myelination in the peripheral nervous system (PNS) “Phosphorylation of cytohesin-1 by Fyn is required for initiation of myelination and the extent of myelination during development (Yamauchi et al., 2015 [1])”. Herein we provide the data regarding myelination-related protein markers and myelin ultrastructure in transgenic mice. Keywords: Fyn, Myelination, Peripheral nervous system, Myelin marker protein, Signalin

Lidocaine as a potential therapeutic option for super-refractory status epilepticus: A case report

New-onset refractory status epilepticus (NORSE) is a rare and devastating condition and the prognosis is often poor, with half to two-thirds of survivors experiencing drug-resistant epilepsy, residual cognitive impairment, or functional disability, and the mortality rate is 16% to 27% for adults. We describe a patient with cryptogenic NORSE and favorable recovery from drug-resistant super-refractory SE after the use of intravenous lidocaine. The patient experienced fever and presented with refractory generalized tonic-clonic seizures. The cause was not found by performing extensive examinations, including cell surface autoantibodies and rat brain immunohistochemistry evaluations. The refractory SE with unresponsiveness to multiple anti-epileptic and prolonged sedative medications, which are necessary for prolonged mechanical ventilation, were ameliorated by additive treatment with intravenous lidocaine initiating at 1 mg/kg/h and maintaining at 2 mg/kg/h for 40 days, which led to freedom from intravenous sedative medication and mechanical ventilation. The patient was able to return to school. Lidocaine may be an optional treatment for cryptogenic NORSE

Electrical biosensing system utilizing ion-producing enzymes conjugated with aptamers for the sensing of severe acute respiratory syndrome coronavirus 2

Viral outbreaks, which include the ongoing coronavirus disease 2019 (COVID-19) pandemic provoked by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), are a major global crisis that enormously threaten human health and social activities worldwide. Consequently, the rapid and repeated treatment and isolation of these viruses to control their spread are crucial to address the COVID-19 pandemic and future epidemics of novel emerging viruses. The application of cost-efficient, rapid, and easy-to-operate detection devices with miniaturized footprints as a substitute for the conventional optic-based polymerase chain reaction (PCR) and immunoassay tests is critical. In this context, semiconductor-based electrical biosensors are attractive sensing platforms for signal readout. Therefore, this study aimed to examine the electrical sensing of patient-derived SARS-CoV-2 samples by harnessing the activity of DNA aptamers directed against spike proteins on viral surfaces. We obtained rapid and sensitive virus detection beyond the Debye length limitation by exploiting aptamers coupled with alkaline phosphatases, which catalytically generate free hydrogen ions which can readily be measured on pH meters or ion-sensitive field-effect transistors. Furthermore, we demonstrated the detection of the viruses of approximately 100 copies/μL in 10 min, surpassing the capability of typical immunochromatographic assays. Therefore, our newly developed technology has great potential for point-of-care testing not only for SARS-CoV-2, but also for other types of pathogens and biomolecules

Spectroscopic Identification of Ag-Terminated “Multilayer Silicene” Grown on Ag(111)

The electronic structure of the outermost layer of “multilayer silicene” was investigated by metastable atom electron spectroscopy (MAES). It is usually difficult to elucidate the electronic structure of an ultrathin film grown on a solid substrate excluding the contribution from the substrate, especially such as “multilayer silicene” grown on a Ag(111) substrate. MAES used in this study thus provides a proper solution because the excitation source, He*­(2³S) atom, cannot penetrate through the first layer. Comparing the MAES spectra of “multilayer silicene” and of the Si(111)√3 × √3-Ag surface where the Ag atoms are arranged to form a superlattice on the (111) surface of the Si diamond crystal, we find that these spectra are essentially identical to each other. This result indicates that the so-called “multilayer silicene” is actually not multilayered, i.e., a stack of honeycomb lattice layers