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Dive into the research topics where Kenji Fukutsuji is active.

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Featured researches published by Kenji Fukutsuji.


Acta Oto-laryngologica | 2008

Superselective angiographic embolization for intractable epistaxis

Kenji Fukutsuji; Suetaka Nishiike; Teruhito Aihara; Masako Uno; Tamotsu Harada; Masayuki Gyoten; Shigeki Imai

Conclusions. Routine embolization of the ipsilateral facial artery (FA) is effective because of the high success rate. The use of different embolic materials for the internal maxillary artery (IMA) and the FA was considered safe because of the absence of major complications. Objective. To evaluate outcomes of routine embolization of the FA as well as the IMA ipsilateral to the bleeding site for intractable epistaxis, and outcomes using different embolic materials for the FA and the IMA. Patients and methods. Twenty-two patients with intractable epistaxis who underwent superselective embolization were retrospectively analyzed with a mean follow-up of 7 months. The FA and the IMA ipsilateral to the bleeding site were embolized. Two embolic materials, gelatin sponge and microcoils, were used for the IMA and the FA, respectively. Results. The short-term success rate within the first 7 days was 77.3% (17/22). The long-term success rate was 95.5% (21/22). There were no major complications in 22 cases. Minor complications occurred in 13 cases (59%). These minor complications usually did not last more than a week and most resolved within a day.


Journal of Immunology | 2014

Does β-Hexosaminidase Function Only as a Degranulation Indicator in Mast Cells? The Primary Role of β-Hexosaminidase in Mast Cell Granules

Nobuyuki Fukuishi; Shinya Murakami; Akane Ohno; Naoya Yamanaka; Nobuaki Matsui; Kenji Fukutsuji; Sakuo Yamada; Kouji Itoh; Masaaki Akagi

β-Hexosaminidase, which is generally present in the lysosome, is essential for glycoprotein metabolism in the maintenance of cell homeostasis. In mast cells (MCs), large amounts of β-hexosaminidase are present in the granules as opposed to the lysosome, and the biological role of MC β-hexosaminidase has yet to be fully elucidated. Therefore, we investigated the biological role of β-hexosaminidase in MC granules. Bone marrow-derived MCs from C57BL/6 (BL/6-BMMC) or β-hexosaminidase gene–deficient (hexb−/−-BMMC) mice were transplanted into MC-deficient (WBB6F1/J-KitW/KitW-v [W/Wv]) mice to generate MC-reconstituted models. In asthma model experiments, no differences were observed in the symptoms of BL/6, W/Wv, BL/6-BMMC–reconstituted W/Wv, or hexb−/−-BMMC–reconstituted W/Wv mice. In Staphylococcus epidermidis experimental infection model experiments, the severity of symptoms and frequency of death were markedly higher in W/Wv and hexb−/−-BMMC–reconstituted W/Wv mice than in BL/6 and BL/6-BMMC–reconstituted W/Wv mice. The growth of S. epidermidis in an in vitro study was clearly inhibited by addition of BL/6-BMMC lysate, but not by addition of hexb−/−-BMMC lysate. Moreover, suppression of bacterial proliferation was completely recovered when bacteria were incubated with hexb−/−-BMMC lysate plus β-hexosaminidase. Transmission electron microscopy indicated that the cell wall of S. epidermidis was heavily degraded following coincubation of bacteria with BL/6-BMMC lysate, but not following coincubation with hexb−/−-BMMC lysate. These findings strongly suggest that MC granule β-hexosaminidase is crucial for defense against bacterial invasion, but is not involved in the allergic response. Our results also suggest that the bactericidal mechanism of β-hexosaminidase involves degradation of bacterial cell wall peptidoglycan.


Infection and Immunity | 2013

The Surface Layer of Tannerella forsythia Contributes to Serum Resistance and Oral Bacterial Coaggregation

Yuichi Oogai; Miki Kawada-Matsuo; Sakuo Yamada; Kenji Fukutsuji; Keiji Nagano; Fuminobu Yoshimura; Kazuyuki Noguchi; Hitoshi Komatsuzawa

ABSTRACT Tannerella forsythia is an anaerobic, Gram-negative bacterium involved in the so-called “red complex,” which is associated with severe and chronic periodontitis. The surface layer (S-layer) of T. forsythia is composed of cell surface glycoproteins, such as TfsA and TfsB, and is known to play a role in adhesion/invasion and suppression of proinflammatory cytokine expression. Here we investigated the association of this S-layer with serum resistance and coaggregation with other oral bacteria. The growth of the S-layer-deficient mutant in a bacterial medium containing more than 20% non-heat-inactivated calf serum (CS) or more than 40% non-heat-inactivated human serum was significantly suppressed relative to that of the wild type (WT). Next, we used confocal microscopy to perform quantitative analysis on the effect of serum. The survival ratio of the mutant exposed to 100% non-heat-inactivated CS (76% survival) was significantly lower than that of the WT (97% survival). Furthermore, significant C3b deposition was observed in the mutant but not in the WT. In a coaggregation assay, the mutant showed reduced coaggregation with Streptococcus sanguinis, Streptococcus salivarius, and Porphyromonas gingivalis but strong coaggregation with Fusobacterium nucleatum. These results indicated that the S-layer of T. forsythia plays multiple roles in virulence and may be associated with periodontitis.


Medical Molecular Morphology | 2013

Thickening of the cell wall in macrolide-resistant Staphylococcus aureus

Yukiyoshi Hyo; Sakuo Yamada; Kenji Fukutsuji; Tamotsu Harada

Macrolides are widely used at low dosage for long-term therapy of chronic sinusitis. Twenty clinical macrolide-resistant Staphylococcus aureus strains were morphologically compared with 10 clinical macrolide-sensitive strains. PCR amplification was performed to determine the presence of four known macrolide resistance genes. Transmission electron microscopy revealed significantly thicker cell walls in clinical macrolide-resistant strains. Even though the ultrastructural characteristics were shared by all macrolide-resistant strains, they were not associated with the presence or absence of the known macrolide-resistance genes. We also demonstrated that macrolide-resistant mutant strains derived in vitro from a macrolide-sensitive parent strain had thickened cell walls and did not harbor the known macrolide-resistance genes. These results, therefore, revealed that macrolide-resistant S. aureus strains have thickened cell walls as a common ultrastructural characteristic and that cell wall thickening is likely mediated by an unknown gene which is unrelated to any known macrolide resistance gene.


Medical Molecular Morphology | 2012

Antimicrobial effects of Burow's solution on Staphylococcus aureus and Pseudomonas aeruginosa

Yukiyoshi Hyo; Sakuo Yamada; Masaki Ishimatsu; Kenji Fukutsuji; Tamotsu Harada

Burow’s solution has been shown to be effective against chronic suppurative otitis media and otitis externa. We demonstrated that Burow’s solution had antibacterial effects against Staphylococcus aureus and Pseudomonas aeruginosa, inducing ultrastructural changes in these bacteria in vitro. S. aureus strain 209P and P. aeruginosa strain IID1130 were treated with 13% Burow’s solution. Viable cell counts were determined to measure bactericidal effects. Ultrastructural changes in cells of both strains were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Viable cell counting revealed that S. aureus cells treated with Burow’s solution were killed within 30 min. The viable cell count of P. aeruginosa was reduced by 1 × 107 colony-forming units/ml (CFU/ml) after a 60-min treatment. SEM examination of S. aureus revealed blebbing on the surface of bacterial cells, whereas TEM revealed undulating deformation of the bacterial cell wall, diluted cytoplasm, and cell membrane detachment. SEM observations of P. aeruginosa revealed a more apparent undulating deformation of the bacterial cell surface. TEM observations also revealed deformations in the bacterial cell wall and diluted cytoplasm in both bacteria. These findings show that Burow’s solution is active against S. aureus and P. aeruginosa, resulting in damage to the cell wall.


Auris Nasus Larynx | 2017

Two cases of thermal burns of the larynx in older men

Yukiyoshi Hyo; Kenji Fukutsuji; Hisaki Fukushima; Tamotsu Harada

Cases of thermal burns of the larynx in infants and in patients with mental illness have been reported, but those in older people are rare. We report two cases of thermal burns of the larynx in older people caused by ingestion of microwave-heated food (meat and potato stew or a bean-jam filled bun). Both patients were users of full dentures. Conservative therapy was effective in one patient, while tracheotomy was performed in the other patient at the time of the initial examination. Hot food is expelled from the mouth as a reflective response, preventing thermal burns of the larynx. However, in older individuals, sense perception is impaired and reflexes are slowed. Further, the oral mucosa is protected if full dentures are placed. Therefore, heat is likely to not be perceived and reflexes occur only after the food has reached the larynx, thereby causing thermal burns of the larynx. The number of such cases may increase as the number of older patients rises in the current aging society. Therefore, raising awareness of such cases is important.


Medical Molecular Morphology | 2013

Ultrastructural cell wall characteristics of clinical gentamycin-resistant Staphylococcus aureus isolates

Kenji Fukutsuji; Sakuo Yamada; Tamotsu Harada


Practica oto-rhino-laryngologica | 2010

The Positive Rate of Animal Allergen-specific IgE Antibodies Assessed in Nasal Allergy Patients Using the CAP-RAST System

Yukiyoshi Hyo; Tamotsu Harada; Shoudai Monjyu; Katsumi Masuda; Kenji Fukutsuji; Takeshi Akisada


Practica oto-rhino-laryngologica | 2017

Six Cases of Forestier’s Disease

Dai Shibata; Kenji Fukutsuji; Mariko Tanaka; Takeshi Akisada; Tamotsu Harada


Practica oto-rhino-laryngologica | 2017

A Case of Schwannoma of the Hard Palate

Kenji Fukutsuji; Norimasa Morita; Hiroaki Tadokoro; Masakazu Hamamoto; Tamotsu Harada

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Dai Shibata

Kawasaki Medical School

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Masako Uno

Kawasaki Medical School

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Sakuo Yamada

Kawasaki Medical School

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