Publications by authors named "Hisato Hayashi"

Objectives: Gene therapy using viral vectors and antibody-based therapies continue to expand within the pharmaceutical market. We evaluated whether Cellhesion VP, a chitin-based material, can be used as 3D culture platform for cell lines used for the production of antibodies and viral vectors.

Results: The results of Cell Counting Kit-8 assay and LDH assay revealed that Cellhesion VP had no adverse effect to Human Embryonic Kidney (HEK) 293, A549 and Chinese hamster ovary (CHO) DG44-Interferon-β (IFN) cells.

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Human vascular smooth muscle cells (SMCs) are adherent cells, and they cannot survive without scaffolds in suspension culture. Here, we aimed to establish a suspension culture of SMCs using the functional biopolymer FP003 and to investigate the proliferation status of the cells. When SMCs were suspension cultured with FP003, their proliferation was inhibited with a viability of 75% until day 15.

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Currently, there are many challenges in the culture of human induced pluripotent stem (iPS) cell-derived intestinal organoids (HIOs) for use in drug discovery, disease research, and regenerative medicine. For example, the main culture method, embedding culture, makes industrial large-scale culture difficult, and Matrigel, which is used for almost all HIO cultures, is not respected for its application in regenerative medicine. To overcome these challenges, we herein propose a new culture method using low concentrations of natural polysaccharides in a suspension culture.

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Spindle assembly is spatially regulated by a chromosome-derived Ran- GTP gradient. Previous work proposed that Ran-GTP activates spindle assembly factors (SAFs) around chromosomes by dissociating inhibitory importins from SAFs. However, it is unclear whether the Ran-GTP gradient equivalently activates SAFs that localize at distinct spindle regions.

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Suspension culture is an important method used in the industrial preparation of pluripotent stem cells (PSCs), for regenerative therapy and drug screening. Generally, a suspension culture requires agitation to keep PSC aggregates suspended and to promote mass transfer, but agitation also causes cell damage. In this study, we investigated the use of a Bingham plastic fluid, supplemented with a polysaccharide-based polymer, to preserve PSCs from cell damage in suspension culture.

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Article Synopsis
  • Evaluating drug pharmacokinetics in the small intestine is essential for developing effective oral medications, and Caco-2 cells are commonly used for preclinical drug absorption tests.
  • However, these cells do not fully mimic the characteristics of normal human intestinal cells, prompting researchers to explore human iPS cell-derived enterocytes (hiPSEs) as a more accurate alternative.
  • The study found that using gellan gum, a soluble dietary fiber, significantly enhanced the differentiation of hiPSEs and improved the expression of genes and enzymes related to drug metabolism, indicating a better model for drug absorption studies.
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A nanocellulose (NC)-containing medium is a promising candidate for cell storage that allows cell floating without any stirring. We here found that the NC medium was spatially heterogeneous in terms of its rheological properties. The characteristic length of the heterogeneity was a few tens of micrometers and it decreased upon sonication treatment.

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Scalable production of avian cell lines exhibits a valuable potential on therapeutic application by producing recombinant proteins and as the substrate for virus growth due to the special glycosylation occurs in avian species. Chicken primordial germ cells (cPGCs), a germinal pluripotent avian cell type, present the ability of self-renewal, an anchorage-independent cell growth and the ability to be genetically modified. This cell type could be an interesting bioreactor system for industrial purposes.

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