MX337982B - Induccion de celulas pluripotentes. - Google Patents
Induccion de celulas pluripotentes.Info
- Publication number
- MX337982B MX337982B MX2012004283A MX2012004283A MX337982B MX 337982 B MX337982 B MX 337982B MX 2012004283 A MX2012004283 A MX 2012004283A MX 2012004283 A MX2012004283 A MX 2012004283A MX 337982 B MX337982 B MX 337982B
- Authority
- MX
- Mexico
- Prior art keywords
- reprogramming
- induction
- human
- pluripotent cells
- methods
- Prior art date
Links
- 230000006698 induction Effects 0.000 title 1
- 210000004263 induced pluripotent stem cell Anatomy 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 230000008672 reprogramming Effects 0.000 abstract 2
- 210000002950 fibroblast Anatomy 0.000 abstract 1
- 210000001082 somatic cell Anatomy 0.000 abstract 1
- 230000003612 virological effect Effects 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0696—Artificially induced pluripotent stem cells, e.g. iPS
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/065—Modulators of histone acetylation
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/60—Transcription factors
- C12N2501/602—Sox-2
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/60—Transcription factors
- C12N2501/603—Oct-3/4
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/60—Transcription factors
- C12N2501/604—Klf-4
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/60—Transcription factors
- C12N2501/606—Transcription factors c-Myc
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/70—Enzymes
- C12N2501/72—Transferases [EC 2.]
- C12N2501/727—Kinases (EC 2.7.)
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2501/00—Active agents used in cell culture processes, e.g. differentation
- C12N2501/999—Small molecules not provided for elsewhere
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2506/00—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells
- C12N2506/09—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from epidermal cells, from skin cells, from oral mucosa cells
- C12N2506/094—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from epidermal cells, from skin cells, from oral mucosa cells from keratinocytes
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- C12N2506/00—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells
- C12N2506/13—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from connective tissue cells, from mesenchymal cells
- C12N2506/1307—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from connective tissue cells, from mesenchymal cells from adult fibroblasts
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2506/00—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells
- C12N2506/28—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from vascular endothelial cells
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N2510/00—Genetically modified cells
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Developmental Biology & Embryology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Transplantation (AREA)
- General Health & Medical Sciences (AREA)
- Cell Biology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Materials For Medical Uses (AREA)
- Peptides Or Proteins (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente invención se refiere a la lenta cinética y baja eficiencia de métodos de reprogramación para generar células madre pluripotentes inducidas (iPSCs) humanas imponen mayores limitaciones en su utilidad en las aplicaciones biomédicas. En la presente describimos una aproximación química que mejora dramáticamente (>200 repliegues) la eficiencia de generación de iPSC a partir de fibroblastos humanos, dentro de siete días de tratamiento. Esto mejorará una base para el desarrollo de métodos no virales más eficientes y más seguros para reprogramar células somáticas humanas.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25254809P | 2009-10-16 | 2009-10-16 | |
PCT/US2010/052896 WO2011047300A1 (en) | 2009-10-16 | 2010-10-15 | Induction of pluripotent cells |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2012004283A MX2012004283A (es) | 2012-06-28 |
MX337982B true MX337982B (es) | 2016-03-30 |
Family
ID=43876590
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2012004283A MX337982B (es) | 2009-10-16 | 2010-10-15 | Induccion de celulas pluripotentes. |
MX2021014919A MX2021014919A (es) | 2009-10-16 | 2012-04-12 | Induccion de celulas pluripotentes. |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2021014919A MX2021014919A (es) | 2009-10-16 | 2012-04-12 | Induccion de celulas pluripotentes. |
Country Status (12)
Country | Link |
---|---|
US (4) | US9005968B2 (es) |
EP (3) | EP2488630B1 (es) |
JP (7) | JP5808331B2 (es) |
CN (3) | CN113621576A (es) |
AU (1) | AU2010306627B2 (es) |
BR (1) | BR112012008848A2 (es) |
CA (3) | CA3194845A1 (es) |
ES (2) | ES2638464T3 (es) |
HK (1) | HK1175811A1 (es) |
MX (2) | MX337982B (es) |
RU (1) | RU2012117719A (es) |
WO (1) | WO2011047300A1 (es) |
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KR101679082B1 (ko) | 2008-03-17 | 2016-11-23 | 더 스크립스 리서치 인스티튜트 | 유도 만능 줄기 세포 생성을 위한 화학적 및 유전적 조합 접근법 |
CN102317442B (zh) | 2008-12-17 | 2014-08-13 | 斯克里普斯研究所 | 干细胞的产生和保持 |
CN113621576A (zh) | 2009-10-16 | 2021-11-09 | 斯克里普斯研究所 | 多能细胞的诱导 |
JP5898086B2 (ja) * | 2009-11-04 | 2016-04-06 | セルラー ダイナミクス インターナショナル, インコーポレイテッド | 化学物質を用いるエピソームリプログラミング |
JP5909482B2 (ja) * | 2010-03-31 | 2016-04-26 | ザ スクリプス リサーチ インスティテュート | 細胞の再プログラム |
EP4438734A2 (en) | 2010-06-14 | 2024-10-02 | The Scripps Research Institute | Reprogramming of cells to a new fate |
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JP6182456B2 (ja) | 2010-12-22 | 2017-08-23 | フェイト セラピューティクス,インコーポレイテッド | 単細胞選別のための細胞培養プラットホームおよびiPSCの再プログラミングの増強 |
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CN102604894B (zh) * | 2012-02-29 | 2014-07-30 | 中国科学院广州生物医药与健康研究院 | 用于制备神经干细胞的培养基及其用途 |
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CN110139130B (zh) * | 2012-10-12 | 2022-09-20 | 佳能株式会社 | 流传输数据的方法、发送和接收视频数据的方法和设备 |
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