Publications by authors named "Masashi Ikeuchi"

In this study, non-electrically controlled SalivaDirect loop-mediated isothermal amplification (NEC-SD-LAMP), which can detect infections by amplifying viral DNA expression in saliva without using electrical control systems, was developed. By this method, only by adding water to the device, viral DNA was extracted from saliva using SalivaDirect, the extracted DNA was amplified via loop-mediated isothermal amplification (LAMP), and the results were visually confirmed. Melting palmitic acid maintained the optimal temperature for the LAMP reaction, as the temperature of palmitic acid is maintained at 62.

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Article Synopsis
  • Mutations in Lamin A/C disrupt the structure of cardiomyocytes and contribute to dilated cardiomyopathy (DCM) by trapping the transcription factor TEAD1 at the nuclear membrane.
  • Advanced techniques like single-cell RNA sequencing and ATAC-seq were used to explore the molecular mechanisms behind these mutations, revealing an issue with gene expression regulation.
  • Targeting the Hippo pathway shows promise for correcting the gene dysregulation caused by these mutations, suggesting a potential treatment avenue for patients with DCM linked to this specific mutation.
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Tissue fibrosis and organ dysfunction are hallmarks of age-related diseases including heart failure, but it remains elusive whether there is a common pathway to induce both events. Through single-cell RNA-seq, spatial transcriptomics, and genetic perturbation, we elucidate that high-temperature requirement A serine peptidase 3 (Htra3) is a critical regulator of cardiac fibrosis and heart failure by maintaining the identity of quiescent cardiac fibroblasts through degrading transforming growth factor-β (TGF-β). Pressure overload downregulates expression of Htra3 in cardiac fibroblasts and activated TGF-β signaling, which induces not only cardiac fibrosis but also heart failure through DNA damage accumulation and secretory phenotype induction in failing cardiomyocytes.

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MicroRNA expression analysis is an important screening tool for the early detection of cancer. In this study, we developed two portable three-dimensional microdevices for multiple singleplex RNA expression analysis by microRNA purification and qRT-PCR as a prototype for point-of-care testing. These microdevices are composed of several types of modules termed 'chemical IC chips'.

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Freezing is recognized as the most effective method of maintaining a stable supply of various cell types for long-term storage. However, cells might be damaged by environmental changes during the freezing process. There are various factors that influence the function of cells cultured after cryopreservation and thawing.

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We can detect cancer in the early stages by validating the expression of cancer specific nucleic acids in the blood. In this report, we have developed the micro device for performing real-time polymerase chain reaction (real-time PCR), one of the methods used for determining the quantity of nucleic acids, using a small volume of reagent. This all-in-one device can perform real-time PCR with the inclusion of heating control and the analyzing system with optical sensor.

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Article Synopsis
  • The study explores the use of human adipose tissue-derived stem cells (ASCs) for cell therapy, highlighting their ability to differentiate into various cell types and their potential for large-scale production with reliable quality.
  • Researchers set up a 3D culture using a microelectromechanical system (TASCL device) to create a favorable environment for inducing adipogenic differentiation of ASC spheroids, achieving better results compared to traditional 2D cultures.
  • The findings indicate that the 3D culture generated "adipose-like microtissues" with enhanced triglyceride accumulation, suggesting valuable applications in regenerative medicine and cell transplantation.
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In drug discovery, it is very important to evaluate liver cells within an organism. Compared to 2D culture methods, the development of 3D culture techniques for liver cells has been successful in maintaining long-term liver functionality with the formation of a hepatic-specific structure. The key to performing drug testing is the establishment of a stable in vitro evaluation system.

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Attempts to create artificial liver tissue from various cells have been reported as an alternative method for liver transplantation and pharmaceutical testing. In the construction of artificial liver tissue, the selection of the cell source is the most important factor. However, if an appropriate environment (in vitro/in vivo) cannot be provided for various cells, it is not possible to obtain artificial liver tissue with the desired function.

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Electrospun nanofibers composed of biodegradable polymers are attractive candidates for cell culture scaffolds in tissue engineering. Their fine-meshed structures, resembling natural extracellular matrices, effectively interact with cell surfaces and promote cell proliferation. The application of electrospinning, however, is limited to two-dimensional (2D) or single tube-like scaffolds, and the fabrication of arbitrary three-dimensional (3D) scaffolds from electrospun nanofibers is still very difficult due to the fibers' continuous and entangled form.

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Induced pluripotent stem (iPS) cells are expected to provide a source of tissue, a renewable cell source for tissue engineering, and a method for in vitro drug screening for patient-specific or disease-specific treatment. A simple technology by which iPS cells can be differentiated effectively and in large quantities is strongly desired. In this paper, a new device (Tapered Soft Stencil for Cluster Culture: TASCL) is proposed for the easy and efficient formation of EBs which can be used in regenerative medicine.

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