发明申请
US20110275157A1 COMPOSITION FOR REPROGRAMMING SOMATIC CELLS TO GENERATE INDUCED PLURIPOTENT STEM CELLS, COMPRISING Bmi1 AND LOW MOLECULAR WEIGHT SUBSTANCE, AND METHOD FOR GENERATING INDUCED PLURIPOTENT STEM CELLS USING THE SAME
有权
用于复制SOMATIC细胞以产生诱导的包含Bmi1和低分子重量物质的诱导型干细胞的组合物,以及用于产生使用其的诱导的细胞干细胞的方法
- 专利标题: COMPOSITION FOR REPROGRAMMING SOMATIC CELLS TO GENERATE INDUCED PLURIPOTENT STEM CELLS, COMPRISING Bmi1 AND LOW MOLECULAR WEIGHT SUBSTANCE, AND METHOD FOR GENERATING INDUCED PLURIPOTENT STEM CELLS USING THE SAME
- 专利标题(中): 用于复制SOMATIC细胞以产生诱导的包含Bmi1和低分子重量物质的诱导型干细胞的组合物,以及用于产生使用其的诱导的细胞干细胞的方法
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申请号: US13103611申请日: 2011-05-09
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公开(公告)号: US20110275157A1公开(公告)日: 2011-11-10
- 发明人: Seungkwon YOU , Jai-Hee MOON , Jun Sung KIM , Byung Sun YOON , Jung Han LEE , Eun Kyoung JUN , June Seok HEO , Ji Hyun KIM , Ji Hye HWANG , Su Hyun GWON
- 申请人: Seungkwon YOU , Jai-Hee MOON , Jun Sung KIM , Byung Sun YOON , Jung Han LEE , Eun Kyoung JUN , June Seok HEO , Ji Hyun KIM , Ji Hye HWANG , Su Hyun GWON
- 申请人地址: KR Seoul
- 专利权人: KOREA UNIVERSITY RESEARCH AND BUSINESS FOUNDATION
- 当前专利权人: KOREA UNIVERSITY RESEARCH AND BUSINESS FOUNDATION
- 当前专利权人地址: KR Seoul
- 优先权: KR10-2010-0043695 20100510; KR10-2010-0043697 20100510; KR10-2010-0043698 20100510
- 主分类号: C12N15/85
- IPC分类号: C12N15/85 ; C12N5/0735
摘要:
Provided is a composition for reprogramming somatic cells to generate embryonic stem cell-like cells, comprising: a) a Bmi1 (B cell-specific Moloney murine leukemia virus integration site 1) protein or a nucleic acid molecule encoding the Bmi1 protein; and b) at least one low molecular weight substance selected from the group consisting of a set of a MEK/ERK (mitogen-activated protein kinase/extracellular regulated kinase) inhibitor and a GSK (glycogen synthase kinase) inhibitor, a set of a G9a HMTase (G9a histone methyltransferase) inhibitor and a DMNT (DNA methyltransferase) inhibitor, and a histone deacetylase inhibitor. Also, a method is provided for reprogramming somatic cells to generate embryonic stem cell-like cells using the composition. In addition to reducing the number of the reprogramming factors conventionally needed, the composition and method allow the generation of pluripotent embryonic stem cell-like cells which have high potential in the cell therapy of various diseases.
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