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Featured researches published by Hajime Sujino.


In Vitro Cellular & Developmental Biology – Animal | 1998

Massive culture of human liver cancer cells in a newly developed radial flow bioreactor system: Ultrafine structure of functionally enhanced hepatocarcinoma cell lines

Masaaki Kawada; I Seishi Nagamori; Hideki Aizaki; Kenichi Fukaya; Minoru Niiya; Tomokazu Matsuura; Hajime Sujino; Satoshi Hasumura; Hitoshi Yashida; Satoru Mizutani; Hiroshi Ikenaga

SummaryWith a view to initiating clinical trials, cell morphology and function for a newly developed artificial liver support system employing highly functional human liver cell line, FLC-7, cultured in a radial flow bioreactor were compared to cells grown in a conventional monolayer culture.The radial flow bioreactor consists of a vertically extended cylindrical matrix comprised of porous glass bead microcarriers through which liquid medium flows from the periphery in toward the central axis generating a beneficial concentration gradient of oxygen and nutrients, while preventing excessive shear stresses or buildup of waste products. The three-dimensional culture system supports high-density (1.1 × 108 cells/ml-matrix), large scale cultures (4.4 × 1010 cells/400 ml-bioreactor) with long-term viability. Scanning and transmission electron microscopy (SEM and TEM) revealed that cells cultured in a monolayer system were flattened and extended with numerous cytoplasmic projections. Cells in the three-dimensional culture were spherical and covered with microvillilike processes resembling liver cells in vivo. The cells were solidly attached on the surfaces and within the pores of the microcarriers in highly dense colonies. The spherical cells remained in close contact with adjacent cells, while circulation of liquid medium flowed freely through spaces between cells. FLC-7 cells produced albumin at a rate of 6.41 µg/24 h/106 cells. Alpha-fetoprotein (AFP) production dropped nearly threefold in comparison to monolayer cultures. Results demonstrated that the new artificial liver support systems (ALSS) provides a superior three-dimensional culture environment that allows cells to perform at naturally functioning levels.


Gastroenterologia Japonica | 1987

Human bile duct carcinoma cell line producing abundant mucinin vitro

Sadamu Homma; Scishi Nagamori; Kiyotaka Fujise; Kazunobu Yamazaki; Satoshi Hasumura; Hajime Sujino; Tomokazu Matsuura; Keiichiro Shimizu; Haruo Kameda; Keizo Takaki

SummaryA human bile duct carcinoma cell line, designated OZ, was established from ascitic effusion of a patient who suffered from obstructive jaundice due to the clogging of the common bile duct with mucinous substances secreted by the cancer cells. OZ was found to be capable of producing mucin in vitro and pools of mucin were macroscopically identified on the monolayer of the cells. On the electron micrographs, cell coat type mucin and abundant intracytoplasmic desmosomes were observed. The OZ cells secreted cardnoembryonic antigen in culture and had high enzymatic activity of γ-glutamyl transpeptidase. The tumor heterotransplanted into nude mice also showed mucin production.


Journal of Gastroenterology | 1995

Heterotopic gastric mucosa of the gallbladder

Shouichi Uchiyama; Shigeru Imai; Atsushi Arita; Kunihiko Takeda; Hajime Sujino; Haruo Kameda

A case of heterotopic gastric mucosa in the fundus of the gallbladder is reported. A 23-year-old man, who had been healthy and asymptomatic, visited our hospital because of abnormal findings in a liver enzyme test given during a routine health screening. Ultrasonography demonstrated a highly echogenic polypoid mass in the fundus of the gallbladder. The gallbladder mass was confirmed by both computed tomography and intravenous cholangiogram. After a 10-month follow up, laparoscopic cholecystectomy was performed. Intraoperative touch smear cytology of this lesion revealed class II cells. The surgical specimen revealed a 15×10×5 mm polypoid lesion in the fundus, with no gallstones in the gallbladder. Histologically, the polypoid lesion consisted of both fundic type and pyloric type gastric glands located in the mucosa of the gallbladder. In the literature, 42 cases of heterotopic gastric mucosa of the gallbladder have been reported, only 3 of which, including this present case, were found incidentally, with no apparent symptoms.


Medical Molecular Morphology | 1994

Morphological changes in human gall bladder carcinoma cell line-NOZ due to epirubicin and doxorubicin.

Masaaki Kawada; Hideki Aizaki; Kenichi Fukaya; Minoru Niiya; Tomokazu Matsuura; Hajime Sujino; Satoshi Hasumura; Seishi Nagamori; Gotaro Toda

Epirubicin is widely used in various cancer therapies because its side effects and less than those of doxorubicin. We compared the direct effects of doxorubicin and epirubicin to cellsin vitro. In this study, we used the human gall bladder carcinoma cell line-NOZ. We evaluated the cytocidal effects using a DNA fluorimetric assay with fluorochrome Hoechst 33342. The addition of epirubicin in a culture medium showed stronger cytocidal effects than the addition of doxorubicin. Morphologically, after treatments with the two drugs, cells were enlarged, large vacuoles appeared in the cytoplasm, and concentrated microvillus-like structures due to doxorubicin were observed by transmission electron microscopy.


Kanzo | 1987

Effects of the combination of hyperthermia and adriamycin on cultured human liver cancer cells.

Kiyotaka Fujise; Seishi Nagamori; Satoshi Hasumura; Sadamu Homma; Hajime Sujino; Tomokazu Matsuura; Keiichirou Shimizu; Minoru Niiya; Haruo Kameda

著者らは抗癌剤の併用による温熱の効果を,著者らの教室にて樹立しえたアルブミン高産生性のヒト肝細胞癌JHH-4株を用い,in vitroにおいて検討を行った.ペトリ皿に付着増殖した肝癌細胞を,抗癌剤として0~20μg/mlのAdriamycinを含む培養液にて,従来のコロニー形成法とは異なり,温度勾配培養装置を用い,37~43℃で2日間培養を行い,生細胞数の算定のみならず機能的,形態的にも判定を行った.温度の上昇に伴い生細胞数の減少,培養上清中のアルブミン濃度の低下,3Hラベルのサイミジン,ウリジン,ロイシンの取込みの低下,付着細胞の形態的変化がみられた.温熱単独でみられた肝癌細胞に対するin vitroにおけるこれらの効果は,Adriamycinを併用することにより増強が認められた.


In Vitro Cellular & Developmental Biology – Plant | 1982

Characterization of alpha-fetoprotein secreted from cultured reuber H-35 hepatoma cells

Seishi Nagamori; Kiyotaka Fujise; Satoshi Hasumura; Sadamu Homma; Hajime Sujino; Haruo Kameda; Hitoshi Endou

SummaryReuber H-35 hepatoma cells were examined for their ability to synthesize protein in vitro, especially to produce alpha-fetoprotein (AFP). The presence of AFP in the culture supernatant solution was determined immunologically by the micro-Ouchterlony method. Charge heterogeneity of AFP was examined electrophoretically in continuous gradient polyacrylamide microgels. With regard to the duration of culture, there was no remarkable change in the ratio of two peaks of AFP, and which came out as a major combined peak and a similar peak by PAS staining on the condition of added SDS. These findings indicated that Reuber H-35 hepatoma cells had potential to produce two charge variants of AFP in vitro.


Experimental Cell Research | 1993

Retinol Transport in Cultured Stellate Cells of Rat Liver: Studies by Light and Electron Microscope Autoradiography

Tomokazu Matsuura; Seishi Nagamori; Satoshi Hasumura; Hajime Sujino; Keiichiro Shimizu; Minoru Niiya; Kazushige Hirosawa


Experimental Cell Research | 1993

Regulation of vitamin A transport into cultured stellate cells of rat liver : studies by anchored cell analysis and sorting system

Tomokazu Matsuura; Seishi Nagamori; Satoshi Hasumura; Hajime Sujino; Minoru Niiya; Keiichiro Shimizu


The Japanese journal of gastro-enterology | 1990

[Analysis for the integrated hepatitis B virus genome in cells of established human hepatocellular carcinoma cell line JHH-7].

Kiyotaka Fujise; Seishi Nagamori; Satoshi Hasumura; Saburo Homma; Kentaro Fujita; Hajime Sujino; Tomokazu Matsuura; Keiji Shimizu; Masami Niiya; Tsuneya Ohno


Kanzo | 1988

The search for the hepatitis B virus genome in cells of human hepatocellular carcinoma cell lines.

Kiyotaka Fujise; Kazunobu Fujita; Seishi Nagamori; Satoshi Hasumura; Sadamu Homma; Hajime Sujino; Tomokazu Matsuura; Keiichirou Shimizu; Minoru Niiya; Tsuneya Ohno; Haruo Kameda

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Satoshi Hasumura

Jikei University School of Medicine

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Tomokazu Matsuura

Jikei University School of Medicine

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Seishi Nagamori

Jikei University School of Medicine

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Kiyotaka Fujise

Jikei University School of Medicine

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Haruo Kameda

Jikei University School of Medicine

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Minoru Niiya

Jikei University School of Medicine

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Sadamu Homma

Jikei University School of Medicine

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Keiichiro Shimizu

Jikei University School of Medicine

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Hideki Aizaki

Jikei University School of Medicine

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Kenichi Fukaya

Jikei University School of Medicine

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