JP2008501795A5 - - Google Patents

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Publication number
JP2008501795A5
JP2008501795A5 JP2007527196A JP2007527196A JP2008501795A5 JP 2008501795 A5 JP2008501795 A5 JP 2008501795A5 JP 2007527196 A JP2007527196 A JP 2007527196A JP 2007527196 A JP2007527196 A JP 2007527196A JP 2008501795 A5 JP2008501795 A5 JP 2008501795A5
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Prior art keywords
cells
stem cell
isolated
extract
culture
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JP2007527196A
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Japanese (ja)
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JP2008501795A (en
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Priority claimed from US10/864,788 external-priority patent/US20050090004A1/en
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Priority claimed from PCT/US2005/005052 external-priority patent/WO2005123123A2/en
Publication of JP2008501795A publication Critical patent/JP2008501795A/en
Publication of JP2008501795A5 publication Critical patent/JP2008501795A5/ja
Withdrawn legal-status Critical Current

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出生後ヒト被験者に由来する生殖細胞系幹細胞培養物を製造する方法であって、該方法は:A method of producing a germline stem cell culture derived from a post-natal human subject, the method comprising:
出生後被験者から生殖細胞サンプルを採取する工程、Collecting a germ cell sample from a postnatal subject,
前記生殖細胞サンプルからc−kitネガティブ且つαC-kit negative and α from the germ cell sample 6 インテグリンポジティブである細胞を単離する工程、Isolating cells that are integrin positive,
単離されたc−kitネガティブ且つαIsolated c-kit negative and α 6 インテグリンポジティブの細胞を、5−アザ−2’−デオキシシチジン、ヒストンデアセチラーゼインヒビター、n−酪酸、トリコスタチンA、細胞全体抽出物、細胞質体抽出物および核質抽出物からなる群から選択される刺激因子を含有する培地で、生育および増殖に有効な条件下で培養することにより、生殖細胞系幹細胞培養物を製造する工程Integrin positive cells are selected from the group consisting of 5-aza-2′-deoxycytidine, histone deacetylase inhibitor, n-butyric acid, trichostatin A, whole cell extract, cytoplast extract and nucleoplasm extract. Producing a germline stem cell culture by culturing in a medium containing a stimulating factor under conditions effective for growth and proliferation
を包含し、Including
該生殖細胞系幹細胞培養物は自己再生およびさらに分化決定された細胞系列へと分化する能力を有する、前記方法。Said method wherein said germline stem cell culture is capable of self-renewal and further differentiation into a determined cell lineage.
幹細胞培養物中の単離されたc−kitネガティブ且つαIsolated c-kit negative and α in stem cell culture 6 インテグリンポジティブの細胞が、Oct−4およびREX1からなる群から選択される少なくとも一つの多能性幹細胞マーカーをさらに発現する、請求項1に記載の方法。The method of claim 1, wherein the integrin positive cells further express at least one pluripotent stem cell marker selected from the group consisting of Oct-4 and REX1. 前記培養工程が、前記単離されたc−kitネガティブ且つαThe culturing step comprises the step of isolating the isolated c-kit negative and α 6 インテグリンポジティブの細胞を、該単離されたc−kitネガティブ且つαIntegrin-positive cells are isolated from the isolated c-kit negative and α 6 インテグリンポジティブの細胞の発達と前記多能性幹細胞マーカーの発現を誘導する刺激因子を含有する培地と接触させる工程を包含する、請求項2に記載の方法。The method according to claim 2, comprising the step of contacting with a medium containing a stimulating factor that induces the development of integrin positive cells and the expression of the pluripotent stem cell marker. 前記生殖細胞が精巣細胞または卵巣細胞である、請求項1に記載の方法。The method of claim 1, wherein the germ cells are testicular cells or ovarian cells. 前記細胞全体抽出物、細胞質体抽出物または核質抽出物が、胚性幹細胞、胎児性幹細胞、成体多能性前駆細胞および始原性細胞からなる群から選択される幹細胞から単離される、請求項1に記載の方法。The whole cell extract, cytoplast extract or nucleoplasm extract is isolated from a stem cell selected from the group consisting of embryonic stem cells, fetal stem cells, adult pluripotent progenitor cells and primordial sex cells. The method according to 1. 請求項1に記載の方法に従って作製された幹細胞培養物。A stem cell culture produced according to the method of claim 1. 単離された、実質的に純粋な、幹細胞の培養物であって、該培養物は:An isolated, substantially pure culture of stem cells, the culture comprising:
少なくとも一つの多能性幹細胞マーカーを発現するc−kitネガティブ且つαC-kit negative and α expressing at least one pluripotent stem cell marker 6 インテグリンポジティブの細胞を含み、該幹細胞培養物は自己再生およびさらに分化決定された細胞系列へ分化する能力を有する、前記培養物。Said culture comprising integrin positive cells, said stem cell culture having the ability to self-renew and further differentiate into a determined cell lineage.
JP2007527196A 2004-06-08 2005-02-16 Therapeutic reprogramming and maturation of hybrid stem cells Withdrawn JP2008501795A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US10/864,788 US20050090004A1 (en) 2003-01-16 2004-06-08 Stem cell maturation for all tissue lines
US58814604P 2004-07-15 2004-07-15
PCT/US2005/005052 WO2005123123A2 (en) 2004-06-08 2005-02-16 Therapeutic reprogramming, hybrid stem cells and maturation

Publications (2)

Publication Number Publication Date
JP2008501795A JP2008501795A (en) 2008-01-24
JP2008501795A5 true JP2008501795A5 (en) 2008-04-03

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JP2007527196A Withdrawn JP2008501795A (en) 2004-06-08 2005-02-16 Therapeutic reprogramming and maturation of hybrid stem cells

Country Status (7)

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EP (1) EP1758989A2 (en)
JP (1) JP2008501795A (en)
AU (1) AU2005253923A1 (en)
BR (1) BRPI0511889A (en)
CA (1) CA2567692A1 (en)
RU (1) RU2006147263A (en)
WO (1) WO2005123123A2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5491871B2 (en) 2007-02-28 2014-05-14 アドビナス セラピュティックス プライベート リミテッド 2,2,2-Trisubstituted acetamide derivatives as glucokinase activators, methods and pharmaceutical applications thereof
EP2155720B1 (en) 2007-06-08 2013-07-17 Advinus Therapeutics Private Limited Pyrrole-2-carboxamide derivatives as glucokinase activators, their process and pharmaceutical application
EP2090649A1 (en) 2008-02-13 2009-08-19 Fondazione Telethon Method for reprogramming differentiated cells
EP2402327B1 (en) 2010-06-29 2018-03-07 Impetis Biosciences Ltd. Acetamide compounds as glucokinase activators, their process and medicinal applications
EP2796873A1 (en) * 2013-04-25 2014-10-29 QGel SA Method for a cell-based drug screening assay and the use thereof

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1100870B1 (en) * 1998-07-31 2008-01-02 Genzyme Corporation Improvement of cardiac function by mesenchymal stem cell transplantation
US20020136709A1 (en) * 2000-12-12 2002-09-26 Nucleus Remodeling, Inc. In vitro-derived adult pluripotent stem cells and uses therefor
JP2004248505A (en) * 2001-09-21 2004-09-09 Norio Nakatsuji Undifferentiated fusion cell of somatic cell derived from es cell deficient in part or all of transplantation antigen and method for producing the same
CA2474766A1 (en) * 2002-01-16 2003-07-31 Chauncey Sayre Stem cell maturation for all tissue types
WO2003102126A1 (en) * 2002-05-31 2003-12-11 Apollo Life Sciences Pty Ltd A method of cell therapy using fused cell hybrids
WO2004046312A2 (en) * 2002-11-15 2004-06-03 The Board Of Trustees Of The University Of Illinois Methods for in vitro expansion of hematopoietic stem cells

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