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  1. 原著論文

Rapid isolation of murine primary hepatocytes for chromosomal analysis

https://repo.qst.go.jp/records/48339
https://repo.qst.go.jp/records/48339
8439ef31-684e-4811-afe2-492cdc2ee9fc
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-09-25
タイトル
タイトル Rapid isolation of murine primary hepatocytes for chromosomal analysis
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Ariyoshi, Kentaro

× Ariyoshi, Kentaro

WEKO 485834

Ariyoshi, Kentaro

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Fujishima, Youhei

× Fujishima, Youhei

WEKO 485835

Fujishima, Youhei

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Miura, Tomisato

× Miura, Tomisato

WEKO 485836

Miura, Tomisato

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Shang, Yi

× Shang, Yi

WEKO 485837

Shang, Yi

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Kakinuma, Shizuko

× Kakinuma, Shizuko

WEKO 485838

Kakinuma, Shizuko

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Shimada, Yoshiya

× Shimada, Yoshiya

WEKO 485839

Shimada, Yoshiya

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Kasai, Kosuke

× Kasai, Kosuke

WEKO 485840

Kasai, Kosuke

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Nakata, Akifumi

× Nakata, Akifumi

WEKO 485841

Nakata, Akifumi

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Tachibana, Akira

× Tachibana, Akira

WEKO 485842

Tachibana, Akira

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A., Yoshida Mitsuaki

× A., Yoshida Mitsuaki

WEKO 485843

A., Yoshida Mitsuaki

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尚 奕

× 尚 奕

WEKO 485844

en 尚 奕

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柿沼 志津子

× 柿沼 志津子

WEKO 485845

en 柿沼 志津子

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島田 義也

× 島田 義也

WEKO 485846

en 島田 義也

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抄録
内容記述タイプ Abstract
内容記述 Primary hepatocyte culture is a crucial tool for investigations of liver function and for evaluating the toxic effects of drugs. In addition, chromosomal analysis of hepatocytes could also prove useful for understanding the mechanisms of hepatocarcinogenesis. However, cultivation of primary hepatocytes for chromosome analysis has been hampered by the specific equipment and skill required to perform the in situ perfusion step necessary for isolation of primary hepatocytes. In the present study, we aimed to establish a simple and efficient method of isolating hepatocytes suitable for chromosome analysis. We performed hepatocyte isolation without using collagenase perfusion, instead digesting liver tissues using collagenase in tubes. In addition, we examined hepatocyte and bone marrow cell (BMC) co-culture and cultivation of hepatocytes with medium containing BMC culture media supernatants. We found that hepatocyte viability and attachment rate were significantly improved, both by co-culture with BMCs and medium containing BMC culture media supernatants, with the later also significantly increasing the mitotic index. Using this simple method of isolation and cultivation we could successfully perform chromosomal analysis of mouse primary hepatocytes. This method has the potential to help understand the mechanisms underlying chromosomal instability mediated hepatocarcinogenesis.
書誌情報 In vitro cellular & Developmental Biology- Animal

巻 53, 号 5, p. 474-478, 発行日 2017-02
出版者
出版者 Springer
ISSN
収録物識別子タイプ ISSN
収録物識別子 1543-706X
DOI
識別子タイプ DOI
関連識別子 10.1007/s11626-017-0132-7
関連サイト
識別子タイプ URI
関連識別子 http://link.springer.com/article/10.1007%2Fs11626-017-0132-7
関連名称 http://link.springer.com/article/10.1007%2Fs11626-017-0132-7
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