• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

诱导多能干细胞与重编程:透过炒作审视科学

Induced pluripotent stem cells and reprogramming: seeing the science through the hype.

作者信息

Izpisúa Belmonte Juan Carlos, Ellis James, Hochedlinger Konrad, Yamanaka Shinya

机构信息

Center of Regenerative Medicine in Barcelona, Dr Aiguader 88, 08003 Barcelona, Spain.

出版信息

Nat Rev Genet. 2009 Dec;10(12):878-83. doi: 10.1038/nrg2700. Epub 2009 Oct 27.

DOI:10.1038/nrg2700
PMID:19859062
Abstract

No-one can have failed to notice the splash that induced pluripotent stem (iPS) cells have made in the few years since somatic cells were first reprogrammed to pluripotency. But what is their real promise, where should research efforts be focused, and are we at a stage where we can replace embryonic stem cells? Four pioneering iPS cell researchers offer their personal insights into these and other questions of current debate. As well expressing hope for the improved understanding and treatment of human disease, they urge caution over safety and propose the establishment of iPS cell banks.

摘要

自体细胞首次被重编程为多能性细胞以来的短短几年间,诱导多能干细胞(iPS细胞)所引起的轰动效应,想必无人能够忽视。但它们真正的前景如何?研究工作应聚焦于何处?我们是否已达到可以替代胚胎干细胞的阶段?四位iPS细胞研究领域的先驱者就这些以及当前辩论中的其他问题分享了他们的个人见解。他们在表达对增进人类疾病理解和治疗的希望的同时,也敦促人们对安全性保持谨慎,并提议建立iPS细胞库。

相似文献

1
Induced pluripotent stem cells and reprogramming: seeing the science through the hype.诱导多能干细胞与重编程:透过炒作审视科学
Nat Rev Genet. 2009 Dec;10(12):878-83. doi: 10.1038/nrg2700. Epub 2009 Oct 27.
2
High throughput sequencing identifies an imprinted gene, Grb10, associated with the pluripotency state in nuclear transfer embryonic stem cells.高通量测序鉴定出一个与核移植胚胎干细胞多能性状态相关的印记基因Grb10。
Oncotarget. 2017 Jul 18;8(29):47344-47355. doi: 10.18632/oncotarget.17185.
3
Trib2 regulates the pluripotency of embryonic stem cells and enhances reprogramming efficiency.Trib2 调节胚胎干细胞的多能性并提高重编程效率。
Exp Mol Med. 2017 Nov 24;49(11):e401. doi: 10.1038/emm.2017.191.
4
Linking incomplete reprogramming to the improved pluripotency of murine embryonal carcinoma cell-derived pluripotent stem cells.将不完全重编程与小鼠胚胎癌细胞来源的多能干细胞的增强多能性联系起来。
PLoS One. 2010 Apr 26;5(4):e10320. doi: 10.1371/journal.pone.0010320.
5
Live fluorescent RNA-based detection of pluripotency gene expression in embryonic and induced pluripotent stem cells of different species.基于活荧光RNA的不同物种胚胎干细胞和诱导多能干细胞中多能性基因表达的检测
Stem Cells. 2015 Feb;33(2):392-402. doi: 10.1002/stem.1872.
6
Primer: induced pluripotency.引物:诱导多能性。
Nat Methods. 2010 Jan;7(1):20-1. doi: 10.1038/nmeth.f.293.
7
iPS cells: potent stuff.诱导多能干细胞:强大的物质。
Nat Methods. 2010 Jan;7(1):17-9. doi: 10.1038/nmeth.f.281.
8
Induced pluripotency: history, mechanisms, and applications.诱导多能性:历史、机制与应用。
Genes Dev. 2010 Oct 15;24(20):2239-63. doi: 10.1101/gad.1963910.
9
Reprogramming of somatic cells after fusion with induced pluripotent stem cells and nuclear transfer embryonic stem cells.体细胞经诱导多能干细胞融合和核移植胚胎干细胞重编程。
Stem Cells Dev. 2010 Feb;19(2):239-46. doi: 10.1089/scd.2009.0142.
10
Identification of spectral modifications occurring during reprogramming of somatic cells.鉴定体细胞重编程过程中发生的光谱变化。
PLoS One. 2012;7(4):e30743. doi: 10.1371/journal.pone.0030743. Epub 2012 Apr 13.

引用本文的文献

1
The function of a heterozygous p53 mutation in a Li-Fraumeni syndrome patient.杂合性 p53 突变在 Li-Fraumeni 综合征患者中的作用。
PLoS One. 2020 Jun 9;15(6):e0234262. doi: 10.1371/journal.pone.0234262. eCollection 2020.
2
Human papillomavirus E7 binds Oct4 and regulates its activity in HPV-associated cervical cancers.人乳头瘤病毒 E7 结合 Oct4 并调节其在 HPV 相关宫颈癌中的活性。
PLoS Pathog. 2020 Apr 16;16(4):e1008468. doi: 10.1371/journal.ppat.1008468. eCollection 2020 Apr.
3
Using induced pluripotent stem cell neuronal models to study neurodegenerative diseases.

本文引用的文献

1
Brains, genes, and primates.大脑、基因与灵长类动物。
Neuron. 2015 May 6;86(3):617-31. doi: 10.1016/j.neuron.2015.03.021.
2
Senescence impairs successful reprogramming to pluripotent stem cells.细胞衰老会损害向多能干细胞的成功重编程。
Genes Dev. 2009 Sep 15;23(18):2134-9. doi: 10.1101/gad.1811609. Epub 2009 Aug 20.
3
Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs.利用患者特异性诱导多能干细胞对家族性自主神经功能异常的发病机制及治疗进行建模。
使用诱导多能干细胞神经元模型来研究神经退行性疾病。
Biochim Biophys Acta Mol Basis Dis. 2020 Apr 1;1866(4):165431. doi: 10.1016/j.bbadis.2019.03.004. Epub 2019 Mar 18.
4
Applications of stem cells and bioprinting for potential treatment of diabetes.干细胞与生物打印在糖尿病潜在治疗中的应用。
World J Stem Cells. 2019 Jan 26;11(1):13-32. doi: 10.4252/wjsc.v11.i1.13.
5
Progenitor cell-based treatment of glial disease.基于祖细胞的胶质疾病治疗。
Prog Brain Res. 2017;231:165-189. doi: 10.1016/bs.pbr.2017.02.010. Epub 2017 Apr 13.
6
A chemical approach to myocardial protection and regeneration.一种心肌保护与再生的化学方法。
Eur Heart J Suppl. 2016 Apr 28;18(Suppl E):E1-E7. doi: 10.1093/eurheartj/suw018. Epub 2016 Apr 29.
7
Untangling the Biology of Genetic Cardiomyopathies with Pluripotent Stem Cell Disease Models.利用多能干细胞疾病模型解析遗传性心肌病的生物学机制
Curr Cardiol Rep. 2017 Apr;19(4):30. doi: 10.1007/s11886-017-0842-1.
8
Rational Development of A Polycistronic Plasmid with A CpG-Free Bacterial Backbone as A Potential Tool for Direct Reprogramming.具有无CpG细菌骨架的多顺反子质粒的合理开发作为直接重编程的潜在工具
Cell J. 2017 Winter;18(4):565-581. doi: 10.22074/cellj.2016.4723. Epub 2016 Sep 26.
9
Cancer stem cells and chemoresistance: The smartest survives the raid.癌症干细胞与化疗耐药性:最聪明的细胞在侵袭中存活下来。
Pharmacol Ther. 2016 Apr;160:145-58. doi: 10.1016/j.pharmthera.2016.02.008. Epub 2016 Feb 17.
10
Application of biomaterials to advance induced pluripotent stem cell research and therapy.生物材料在推进诱导多能干细胞研究与治疗中的应用。
EMBO J. 2015 Apr 15;34(8):987-1008. doi: 10.15252/embj.201490756. Epub 2015 Mar 12.
Nature. 2009 Sep 17;461(7262):402-6. doi: 10.1038/nature08320. Epub 2009 Aug 19.
4
Suppression of induced pluripotent stem cell generation by the p53-p21 pathway.p53-p21 通路对诱导多能干细胞生成的抑制作用。
Nature. 2009 Aug 27;460(7259):1132-5. doi: 10.1038/nature08235. Epub 2009 Aug 9.
5
Immortalization eliminates a roadblock during cellular reprogramming into iPS cells.永生化消除了细胞重编程为诱导多能干细胞过程中的一个障碍。
Nature. 2009 Aug 27;460(7259):1145-8. doi: 10.1038/nature08285. Epub 2009 Aug 9.
6
A p53-mediated DNA damage response limits reprogramming to ensure iPS cell genomic integrity.p53介导的DNA损伤反应限制重编程以确保诱导多能干细胞基因组的完整性。
Nature. 2009 Aug 27;460(7259):1149-53. doi: 10.1038/nature08287. Epub 2009 Aug 9.
7
The Ink4/Arf locus is a barrier for iPS cell reprogramming.Ink4/Arf基因座是诱导多能干细胞重编程的一个障碍。
Nature. 2009 Aug 27;460(7259):1136-9. doi: 10.1038/nature08290. Epub 2009 Aug 9.
8
Linking the p53 tumour suppressor pathway to somatic cell reprogramming.将p53肿瘤抑制通路与体细胞重编程联系起来。
Nature. 2009 Aug 27;460(7259):1140-4. doi: 10.1038/nature08311. Epub 2009 Aug 9.
9
Variation in the safety of induced pluripotent stem cell lines.诱导多能干细胞系安全性的差异。
Nat Biotechnol. 2009 Aug;27(8):743-5. doi: 10.1038/nbt.1554. Epub 2009 Jul 9.
10
Disease-corrected haematopoietic progenitors from Fanconi anaemia induced pluripotent stem cells.来自范可尼贫血诱导多能干细胞的疾病校正造血祖细胞。
Nature. 2009 Jul 2;460(7251):53-9. doi: 10.1038/nature08129. Epub 2009 May 31.