• 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

谱系指定因子:多能性诱导中的新角色

Lineage specifiers: new players in the induction of pluripotency.

机构信息

The MOE Key Laboratory of Cell Proliferation and Differentiation, College of Life Sciences, Peking University, Beijing 100871, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China.

出版信息

Genomics Proteomics Bioinformatics. 2013 Oct;11(5):259-63. doi: 10.1016/j.gpb.2013.09.005. Epub 2013 Oct 4.

DOI:10.1016/j.gpb.2013.09.005
PMID:24095709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4357841/
Abstract

Pluripotency-associated factors and their rivals, lineage specifiers, have long been considered the determining factors for the identity of pluripotent and differentiated cells, respectively. Therefore, factors that are employed for cellular reprogramming in order to induce pluripotency have been identified mainly from embryonic stem cell (ESC)-enriched and pluripotency-associated factors. Recently, lineage specifiers have been identified to play important roles in orchestrating the process of restoring pluripotency. In this review, we summarize the latest discoveries regarding cell fate conversion using pluripotency-associated factors and lineage specifiers. We highlight the value of the "seesaw" model in defining cellular identity, opening up a novel scenario to consider pluripotency and lineage specification.

摘要

多能性相关因子及其对手,谱系指定因子,长期以来一直被认为分别是多能性和分化细胞身份的决定因素。因此,为了诱导多能性而用于细胞重编程的因子主要来自胚胎干细胞(ESC)富集和多能性相关因子。最近,谱系指定因子被确定在协调恢复多能性的过程中发挥重要作用。在这篇综述中,我们总结了使用多能性相关因子和谱系指定因子进行细胞命运转换的最新发现。我们强调了“跷跷板”模型在定义细胞身份方面的价值,为考虑多能性和谱系指定开辟了一个新的场景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9f/4357841/1285f76ff695/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9f/4357841/4e43a61935ef/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9f/4357841/1285f76ff695/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9f/4357841/4e43a61935ef/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb9f/4357841/1285f76ff695/gr1.jpg

相似文献

1
Lineage specifiers: new players in the induction of pluripotency.谱系指定因子:多能性诱导中的新角色
Genomics Proteomics Bioinformatics. 2013 Oct;11(5):259-63. doi: 10.1016/j.gpb.2013.09.005. Epub 2013 Oct 4.
2
Induction of pluripotency in mouse somatic cells with lineage specifiers.用谱系特异性蛋白诱导小鼠体细胞多能性。
Cell. 2013 May 23;153(5):963-75. doi: 10.1016/j.cell.2013.05.001.
3
Cell fate conversion-from the viewpoint of small molecules and lineage specifiers.细胞命运转变——从小分子和谱系决定因子的角度看。
Diabetes Obes Metab. 2016 Sep;18 Suppl 1:3-9. doi: 10.1111/dom.12717.
4
Induced pluripotency for translational research.诱导多能性用于转化研究。
Genomics Proteomics Bioinformatics. 2013 Oct;11(5):288-93. doi: 10.1016/j.gpb.2013.08.001. Epub 2013 Sep 19.
5
GATA family members as inducers for cellular reprogramming to pluripotency.GATA家族成员作为细胞重编程为多能性的诱导因子。
Cell Res. 2015 Feb;25(2):169-80. doi: 10.1038/cr.2015.6. Epub 2015 Jan 16.
6
New balance in pluripotency: reprogramming with lineage specifiers.多能性的新平衡:谱系特化因子重编程。
Cell. 2013 May 23;153(5):939-40. doi: 10.1016/j.cell.2013.04.051.
7
Insulin receptor-mediated signaling regulates pluripotency markers and lineage differentiation.胰岛素受体介导的信号转导调节多能性标志物和谱系分化。
Mol Metab. 2018 Dec;18:153-163. doi: 10.1016/j.molmet.2018.09.003. Epub 2018 Sep 19.
8
Fusion of Reprogramming Factors Alters the Trajectory of Somatic Lineage Conversion.重编程因子的融合改变了体细胞核移植的轨迹。
Cell Rep. 2019 Apr 2;27(1):30-39.e4. doi: 10.1016/j.celrep.2019.03.023.
9
microRNAs: important regulators of stem cells.微小RNA:干细胞的重要调节因子。
Stem Cell Res Ther. 2017 May 11;8(1):110. doi: 10.1186/s13287-017-0551-0.
10
Embryonic stem cell and induced pluripotent stem cell: an epigenetic perspective.胚胎干细胞和诱导多能干细胞:表观遗传学视角。
Cell Res. 2013 Jan;23(1):49-69. doi: 10.1038/cr.2012.175. Epub 2012 Dec 18.

引用本文的文献

1
Generation and clinical potential of functional T lymphocytes from gene-edited pluripotent stem cells.基因编辑多能干细胞来源的功能性T淋巴细胞的产生及其临床潜力
Exp Hematol Oncol. 2022 May 14;11(1):27. doi: 10.1186/s40164-022-00285-y.
2
Cell-by-cell dissection of phloem development links a maturation gradient to cell specialization.对韧皮部发育进行逐个细胞的剖析,将成熟梯度与细胞特化联系起来。
Science. 2021 Dec 24;374(6575):eaba5531. doi: 10.1126/science.aba5531.
3
Directed Evolution of an Enhanced POU Reprogramming Factor for Cell Fate Engineering.

本文引用的文献

1
Reprogramming of human fibroblasts to pluripotency with lineage specifiers.人成纤维细胞重编程为多能性细胞与谱系特异性蛋白。
Cell Stem Cell. 2013 Sep 5;13(3):341-50. doi: 10.1016/j.stem.2013.06.019. Epub 2013 Jul 18.
2
Induction of pluripotency in mouse somatic cells with lineage specifiers.用谱系特异性蛋白诱导小鼠体细胞多能性。
Cell. 2013 May 23;153(5):963-75. doi: 10.1016/j.cell.2013.05.001.
3
Single-cell expression analyses during cellular reprogramming reveal an early stochastic and a late hierarchic phase.单细胞表达分析在细胞重编程过程中揭示了早期的随机和晚期的层次阶段。
定向进化增强的 POU 重编程因子用于细胞命运工程。
Mol Biol Evol. 2021 Jun 25;38(7):2854-2868. doi: 10.1093/molbev/msab075.
4
Excluding Oct4 from Yamanaka Cocktail Unleashes the Developmental Potential of iPSCs.从山中因子组合中去除Oct4可释放诱导多能干细胞的发育潜能。
Cell Stem Cell. 2019 Dec 5;25(6):737-753.e4. doi: 10.1016/j.stem.2019.10.002. Epub 2019 Nov 7.
5
SeesawPred: A Web Application for Predicting Cell-fate Determinants in Cell Differentiation.SeesawPred:一个用于预测细胞分化中细胞命运决定因素的网络应用程序。
Sci Rep. 2018 Sep 6;8(1):13355. doi: 10.1038/s41598-018-31688-9.
6
p53 switches off pluripotency on differentiation.p53在细胞分化时关闭多能性。
Stem Cell Res Ther. 2017 Feb 28;8(1):44. doi: 10.1186/s13287-017-0498-1.
7
GATA family members as inducers for cellular reprogramming to pluripotency.GATA家族成员作为细胞重编程为多能性的诱导因子。
Cell Res. 2015 Feb;25(2):169-80. doi: 10.1038/cr.2015.6. Epub 2015 Jan 16.
8
Reprogramming by lineage specifiers: blurring the lines between pluripotency and differentiation.谱系决定因子介导的重编程:模糊多能性与分化之间的界限
Curr Opin Genet Dev. 2014 Oct;28:57-63. doi: 10.1016/j.gde.2014.09.009. Epub 2014 Oct 14.
9
Differential response of epiblast stem cells to Nodal and Activin signalling: a paradigm of early endoderm development in the embryo.上胚层干细胞对Nodal和激活素信号的差异反应:胚胎早期内胚层发育的范例
Philos Trans R Soc Lond B Biol Sci. 2014 Dec 5;369(1657). doi: 10.1098/rstb.2013.0550.
10
From blastocyst to gastrula: gene regulatory networks of embryonic stem cells and early mouse embryogenesis.从囊胚到原肠胚:胚胎干细胞的基因调控网络与小鼠早期胚胎发育
Philos Trans R Soc Lond B Biol Sci. 2014 Dec 5;369(1657). doi: 10.1098/rstb.2013.0542.
Cell. 2012 Sep 14;150(6):1209-22. doi: 10.1016/j.cell.2012.08.023.
4
Direct reprogramming of mouse and human fibroblasts into multipotent neural stem cells with a single factor.将小鼠和人成纤维细胞直接重编程为具有单一因子的多能神经干细胞。
Cell Stem Cell. 2012 Jul 6;11(1):100-9. doi: 10.1016/j.stem.2012.05.018. Epub 2012 Jun 7.
5
Distinct lineage specification roles for NANOG, OCT4, and SOX2 in human embryonic stem cells.在人类胚胎干细胞中,NANOG、OCT4 和 SOX2 具有不同的谱系特化作用。
Cell Stem Cell. 2012 Apr 6;10(4):440-54. doi: 10.1016/j.stem.2012.02.016.
6
Direct conversion of fibroblasts into stably expandable neural stem cells.成纤维细胞直接转化为稳定扩增的神经干细胞。
Cell Stem Cell. 2012 Apr 6;10(4):473-9. doi: 10.1016/j.stem.2012.03.003. Epub 2012 Mar 22.
7
Direct reprogramming of fibroblasts into neural stem cells by defined factors.通过定义因子将成纤维细胞直接重编程为神经干细胞。
Cell Stem Cell. 2012 Apr 6;10(4):465-72. doi: 10.1016/j.stem.2012.02.021. Epub 2012 Mar 22.
8
The promise of induced pluripotent stem cells in research and therapy.诱导多能干细胞在研究和治疗中的应用前景。
Nature. 2012 Jan 18;481(7381):295-305. doi: 10.1038/nature10761.
9
Direct lineage conversions: unnatural but useful?直接谱系转换:非自然但有用?
Nat Biotechnol. 2011 Oct;29(10):892-907. doi: 10.1038/nbt.1946.
10
Pluripotency factors in embryonic stem cells regulate differentiation into germ layers.胚胎干细胞中的多能性因子调节向胚层的分化。
Cell. 2011 Jun 10;145(6):875-89. doi: 10.1016/j.cell.2011.05.017.