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Publication
Featured researches published by Kensuke Yasui.
Journal of Cellular and Molecular Medicine | 2008
Norihisa Okada; Yoko Ishigami; Takuji Suzuki; Akihiro Kaneko; Kensuke Yasui; Ryuuta Fukutomi; Mamoru Isemura
• Introduction • Importins and exportins • NLS and NES • Cargo molecules • Importins and exportins In cellular differentiation ‐ HL‐60 cell differentiation ‐ Importin expression ‐ Exportèn expression ‐ Monocyte differentiation ‐ Terminal erythroìd differentiation ‐ Neural differentiation ‐ Cardiac differentiation ‐ Keratìnocyte differentiation ‐ Germ cell maturation ‐ Muscle cell differentiation • Concluding remarks
Scientific Reports | 2015
Keiko Tanaka; Yasushi Ohgo; Yuki Katayanagi; Kensuke Yasui; Shigeru Hiramoto; Hiroyuki Ikemoto; Yumi Nakata; Noriyuki Miyoshi; Mamoru Isemura; Norio Ohashi; Shinjiro Imai
We conducted a preliminary investigation of the effects of visible light irradiation on plant extracts, and we observed a strong suppressive effect on interleukin (IL) 2 expression with the inhibition of c-Jun amino-terminal kinase (JNK) phosphorylation in Jurkat cells by visible light irradiation to ethanol extract from green soybeans (LIEGS). This effect was produced only by extracts from green soybeans (Glycine max) and not other-color soybeans. LIEGS suppressed the lipopolysaccharide-induced IL-6, IL-12 and TNF-α expression levels in human monocyte THP-1 cells in a concentration-dependent manner. LIEGS was applied for 8 weeks to NC/Nga mice. LIEGS suppressed the development of atopic dermatitis (AD)-like skin lesions and reduced the dermatitis scores of the mice. The light irradiation changed the various types of small-molecule compounds in extracts. Visible light irradiation to daidzein with chlorophyll b induced a novel oxidative product of daidzein. This product suppressed IL-2 expression in Jurkat cells.
Food Chemistry | 2013
Yuki Katayanagi; Kensuke Yasui; Hiroyuki Ikemoto; Kyoko Taguchi; Ryuta Fukutomi; Mamoru Isemura; Tsutomu Nakayama; Shinjiro Imai
The present study was performed to investigate the immune-modulating activities of extracts from green soybean (Glycine max) in a 2,4-toluene diisocyanate (TDI)-inducing guinea pig rhinitis model and a human trial study for allergic rhinitis. Hot water extracts of green soybean were chosen for animal experimentation on the basis of their ability to regulate the production of B cell-activating factor of the TNF family and a proliferation-inducing ligand in mouse spleen cells. Green soybean extracts significantly decreased the levels of ovalubumin (OVA)-specific IgE in mice and significantly suppressed the TDI-induced nasal mucosa secretion. An open-label human pilot study was performed on 16 subjects, using Japanese cedar pollinosis. The symptom scores for Japanese cedar pollinosis were better in the long-term green soybean extracts intake group than in the withdrawal short-term intake group. Green soybean extracts had great potential as an orally active immune modulator for the treatment of various allergic diseases.
Journal of Medicinal Food | 2011
Kensuke Yasui; Noriyuki Miyoshi; Hiroki Tababe; Yoko Ishigami; Ryuuta Fukutomi; Shinjiro Imai; Mamoru Isemura
Tea has many beneficial effects. We have previously reported that green tea and a catechin-rich green tea beverage modulated the gene expression of the gluconeogenic enzymes glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (PEPCK) in the normal murine liver. In the present study, we examined the effects of oral administration of oolong tea on the hepatic expression of gluconeogenesis-related genes in the mouse. The intake of oolong tea for 4 weeks reduced the hepatic expression of G6Pase and PEPCK together with that of the transcription factor hepatocyte nuclear factor (HNF) 4α. When rat hepatoma H4IIE cells were incubated in the presence of oolong tea, the expression of these genes was repressed in accordance with the findings in vivo. The reduced protein expression of PEPCK and HNF4α was also demonstrated. We then fractionated oolong tea by sequential extraction with three organic solvents to give three fractions and the residual fraction (Fraction IV). In addition to organic fractions, Fraction IV, which was devoid of low-molecular-weight catechins such as (-)-epigallocatechin gallate (EGCG), had effects similar to those of oolong tea on H4IIE cells. Fraction IV repressed the gene expression of insulin-like growth factor binding protein 1, as insulin did. This activity was different from that of EGCG. The present findings suggest that drinking oolong tea may help to prevent diabetes and that oolong tea contains a component or components with insulin-like activity distinguishable from EGCG. Identification of such component(s) may open the way to developing a new drug for diabetes.
Journal of the Science of Food and Agriculture | 2012
Monira Pervin; Noriko Paeng; Kensuke Yasui; Shinjiro Imai; Mamoru Isemura; Hidehiko Yokogoshi; Tsutomu Nakayama
BACKGROUND Lectins are proteins that bind specifically to the carbohydrate moiety of glyco-conjugates. Japanese mistletoe lectin given intragastrically affected cytokine gene expression in the mouse intestine. This study examines the actions of Lens culinaris agglutinin (LCA) on the gene expression of gluconeogenic enzymes in the intestine. RESULTS The results of quantitative real-time reverse transcription-polymerase chain reaction indicated that LCA caused an up-regulation of the gene expression of glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (PEPCK). This change was correlated with an increase in the expression of two transcription factors, HNF1α and HNF4α. Experiments using human colonic cancer Caco-2 cells demonstrated that LCA up-regulated the gene expression of G6Pase and PEPCK whereas insulin had the opposite effect. In addition, the observed up-regulation of HNF4α gene expression in the duodenum raises the possibility that the lectin promotes the colorectal cancer. CONCLUSION Lentil beans should be cooked well to avoid unfavourable effects of LCA.
Biomedical Research-tokyo | 2009
Koichi Abe; Norihisa Okada; Hiroki Tanabe; Ryuuta Fukutomi; Kensuke Yasui; Mamoru Isemura; Naohide Kinae
Biomedical Research-tokyo | 2012
Kensuke Yasui; Noriko Paeng; Noriyuki Miyoshi; Takuji Suzuki; Kyoko Taguchi; Yoko Ishigami; Ryuuta Fukutomi; Shinjiro Imai; Mamoru Isemura; Tsutomu Nakayama
Biomedical Research-tokyo | 2010
Kensuke Yasui; Hiroki Tanabe; Norihisa Okada; Ryuuta Fukutomi; Yoko Ishigami; Mamoru Isemura
Biomedical Research-tokyo | 2009
Norihisa Okada; Hiroki Tanabe; Hideaki Tazoe; Yoko Ishigami; Ryuuta Fukutomi; Kensuke Yasui; Mamoru Isemura
Biomedical Research-tokyo | 2011
Kensuke Yasui; Hiroki Tanabe; Noriyuki Miyoshi; Takuji Suzuki; Shingo Goto; Kyoko Taguchi; Yoko Ishigami; Noriko Paeng; Ryuuta Fukutomi; Shinjiro Imai; Mamoru Isemura