JP2009100702A5 - - Google Patents

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Publication number
JP2009100702A5
JP2009100702A5 JP2007277285A JP2007277285A JP2009100702A5 JP 2009100702 A5 JP2009100702 A5 JP 2009100702A5 JP 2007277285 A JP2007277285 A JP 2007277285A JP 2007277285 A JP2007277285 A JP 2007277285A JP 2009100702 A5 JP2009100702 A5 JP 2009100702A5
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Japan
Prior art keywords
cells
hepatoblasts
medium
embryonic stem
stem cells
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JP2007277285A
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Japanese (ja)
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JP5257971B2 (en
JP2009100702A (en
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Priority to JP2007277285A priority Critical patent/JP5257971B2/en
Priority claimed from JP2007277285A external-priority patent/JP5257971B2/en
Publication of JP2009100702A publication Critical patent/JP2009100702A/en
Publication of JP2009100702A5 publication Critical patent/JP2009100702A5/ja
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Claims (4)

胚性幹細胞から肝芽細胞を分化誘導し、かつ胚性幹細胞から分化した肝芽細胞を含む細胞群から実質的に肝芽細胞群を得る方法であって、
(a)胚性幹細胞から胚様体を形成する工程、及び
(b)該胚様体を下記の培地:
・該培地は、肝細胞の成育に必須である1以上の物質を実質的に含まない
・該物質は、肝細胞の細胞に存在しかつ該細胞群に含まれる肝細胞の細胞以外の細胞には存在しない代謝酵素の産物である
・該培地は、該代謝酵素が該産物を生成するための基質を含む
で胚様体形成開始4日以後に培養する工程を含む方法。
A method of inducing differentiation of hepatoblasts from embryonic stem cells and obtaining a group of hepatoblasts substantially from a group of cells comprising hepatoblasts differentiated from embryonic stem cells,
(A) a step of forming an embryoid body from embryonic stem cells, and (b) the embryoid body in the following medium:
The medium is substantially free of one or more substances essential for hepatocyte growth. The substance is present in hepatocyte cells and is present in cells other than hepatocyte cells contained in the cell group. Is a product of a non-existing metabolic enzyme. The method wherein the medium comprises a step of culturing 4 days after the start of embryoid body formation, wherein the metabolic enzyme contains a substrate for producing the product.
胚性幹細胞から肝芽細胞を分化誘導し、かつ胚性幹細胞から分化した肝芽細胞を含む細胞群から実質的に肝芽細胞群を得る方法であって、
(a)胚性幹細胞から胚様体を形成する工程、及び
(b)該胚様体を下記の培地:
・該培地は、肝細胞の成育に必須であるL−アルギニン、L−チロシン、及びピルビン酸からなる群から選ばれる1以上の物質を実質的に含まない
・該培地は、さらにD−グルコースを実質的に含まず、L−プロリンを含む
・該培地は、肝細胞の細胞に存在する代謝酵素が代謝産物を生成するための、上記以外の基質を含む
で胚様体形成開始4日以後に培養する工程を含む方法。
A method of inducing differentiation of hepatoblasts from embryonic stem cells and obtaining a group of hepatoblasts substantially from a group of cells comprising hepatoblasts differentiated from embryonic stem cells,
(A) a step of forming an embryoid body from embryonic stem cells, and (b) the embryoid body in the following medium:
The medium is substantially free of one or more substances selected from the group consisting of L-arginine, L-tyrosine, and pyruvate that are essential for hepatocyte growth. The medium further contains D-glucose. Substantially free, including L-proline
-The medium comprises a step of culturing at least 4 days after the start of embryoid body formation , containing a substrate other than the above, so that a metabolic enzyme present in hepatocyte cells produces a metabolite .
胚性幹細胞から肝芽細胞を分化誘導し、かつ胚性幹細胞から分化した肝芽細胞を含む細胞群から実質的に肝芽細胞群を得る方法であって、
(a)胚性幹細胞から胚様体を形成する工程、及び
(b)該胚様体を下記の培地:
・該培地は、肝細胞の成育に必須であるL−アルギニン、L−チロシン、及びピルビン酸を実質的に含まない
・該培地は、さらにD−グルコースおよびL−シスチンを実質的に含まず、L−プロリンを含む
・該培地は、肝細胞の細胞に存在する代謝酵素が代謝産物を生成するための、上記以外の基質を含む
で胚様体形成開始4日以後に培養する工程を含む方法。
A method of inducing differentiation of hepatoblasts from embryonic stem cells and obtaining a group of hepatoblasts substantially from a group of cells comprising hepatoblasts differentiated from embryonic stem cells,
(A) a step of forming an embryoid body from embryonic stem cells, and (b) the embryoid body in the following medium:
The medium is substantially free of L-arginine, L-tyrosine, and pyruvate essential for hepatocyte growth. The medium is further free of D-glucose and L-cystine. Contains L-proline
· The medium, the method comprising for metabolic enzymes present in cells of the liver cells to produce a metabolite, a step of culturing the embryoid bodies formed after 4 days after in <br/> comprising a substrate other than the above.
請求項1〜3のいずれか1項に記載の方法により得られた実質的に肝芽細胞からなる細胞培養物。
A cell culture substantially consisting of hepatoblasts obtained by the method according to any one of claims 1 to 3.
JP2007277285A 2007-10-25 2007-10-25 Method for obtaining hepatoblasts from embryonic stem cells Expired - Fee Related JP5257971B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007277285A JP5257971B2 (en) 2007-10-25 2007-10-25 Method for obtaining hepatoblasts from embryonic stem cells

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007277285A JP5257971B2 (en) 2007-10-25 2007-10-25 Method for obtaining hepatoblasts from embryonic stem cells

Publications (3)

Publication Number Publication Date
JP2009100702A JP2009100702A (en) 2009-05-14
JP2009100702A5 true JP2009100702A5 (en) 2010-12-16
JP5257971B2 JP5257971B2 (en) 2013-08-07

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007277285A Expired - Fee Related JP5257971B2 (en) 2007-10-25 2007-10-25 Method for obtaining hepatoblasts from embryonic stem cells

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JP (1) JP5257971B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012056997A1 (en) * 2010-10-28 2012-05-03 国立大学法人熊本大学 Method and culture medium for improving pluripotent stem cell differentiation inducing efficiency
WO2013183571A1 (en) * 2012-06-08 2013-12-12 公立大学法人名古屋市立大学 Method for inducing differentiation of artificial pluripotent stem cell into hepatocyte
JP6351018B2 (en) * 2014-02-21 2018-07-04 国立大学法人 熊本大学 Stem cell differentiation induction method using amino acid composition modified medium, and medium kit containing the medium
US10006005B2 (en) * 2014-06-27 2018-06-26 National University Corporation Chiba University Culture medium and method for inducing differentiation of pluripotent stem cells to hepatoblasts
WO2016027850A1 (en) 2014-08-21 2016-02-25 味の素株式会社 Culture medium for mesenchymal stem cells

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4759723B2 (en) * 2004-03-12 2011-08-31 国立大学法人 千葉大学 Method for obtaining target cells from embryonic stem cells

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