Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Lineage Commitment01:21

Lineage Commitment

3.0K
Commitment is the  process whereby stem cells:
3.0K
Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

2.2K
Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
2.2K
Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

1.8K
Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for...
1.8K
iPS Cell Differentiation01:22

iPS Cell Differentiation

2.7K
The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
2.7K
Forced Transdifferentiation01:28

Forced Transdifferentiation

1.9K
Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
Artificial...
1.9K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Programming human cell fate: overcoming challenges and unlocking potential through technological breakthroughs.

Development (Cambridge, England)·2023
Same author

GATA2 mitotic bookmarking is required for definitive haematopoiesis.

Nature communications·2023
Same author

The 2022 International Society for Stem Cell Research (ISSCR) Annual Meeting: Celebrating 20 Years of Achievements.

Cellular reprogramming·2022
Same author

Novel Interplay between p53 and HO-1 in Embryonic Stem Cells.

Cells·2021

相关实验视频

Updated: Jul 19, 2025

De Novo Generation of Somatic Stem Cells by YAP/TAZ
13:05

De Novo Generation of Somatic Stem Cells by YAP/TAZ

Published on: May 7, 2018

9.1K

释放Ascl1:探索在重编程和再生边界中的跨血统潜力

Camila Vazquez Echegaray1

  • 1Department of Laboratory Medicine, Division of Molecular Medicine and Gene Therapy, Lund Stem Cell Centre, Wallenberg Centre for Molecular Medicine, Lund University, Lund, Sweden.

Cellular reprogramming
|August 17, 2023
PubMed
概括

转录因子Ascl1显示出令人惊的多功能性,将非神经细胞重新编程成其已知的神经功能之外的多种血统. 这一发现推动了干细胞研究和再生医学的潜力.

科学领域:

  • 干细胞生物学 干细胞生物学
  • 再生医学是一种再生医学.
  • 分子生物学分子生物学

背景情况:

  • 了解细胞重编程是再生医学的关键.
  • Ascl1 (Achaete-scute家族基本螺旋-循环-螺旋转录因子1) 主要以其在神经发生中的作用而闻名.
  • 控制细胞命运决定的调节网络是复杂的.

研究的目的:

  • 调查Ascl1.1的跨血统潜力.
  • 为了在不同细胞系中比较regularomes (转录因子的DNA结合位点的完整集合).
  • 探索Ascl1在细胞重编程中超越神经发生的作用.

主要方法:

  • 来自不同细胞类型的调节体的比较分析.
  • 对Ascl1表达的实验操纵.
  • 对细胞系转换效率的评估.

主要成果:

  • Ascl1证明了将非神经细胞重新编程成各种血统的能力,而不仅仅是神经命运.
  • 该研究确定了由Ascl1.1.针对的保存和血统特定的监管元素.
  • Ascl1的调节组在不同细胞类型之间有显著的变化,这解释了其多样化的潜力.
关键词:
亚斯克尔1 亚斯克尔1 亚斯克尔1这就是Mef2cc.直接重新编程是直接的重编程.表观遗传学是指表观遗传学.监管机构 监管机构 监管机构

更多相关视频

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts
09:29

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts

Published on: March 22, 2017

7.5K
Live Imaging Followed by Single Cell Tracking to Monitor Cell Biology and the Lineage Progression of Multiple Neural Populations
10:55

Live Imaging Followed by Single Cell Tracking to Monitor Cell Biology and the Lineage Progression of Multiple Neural Populations

Published on: December 16, 2017

8.7K

相关实验视频

Last Updated: Jul 19, 2025

De Novo Generation of Somatic Stem Cells by YAP/TAZ
13:05

De Novo Generation of Somatic Stem Cells by YAP/TAZ

Published on: May 7, 2018

9.1K
Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts
09:29

Assessing Cardiomyocyte Subtypes Following Transcription Factor-mediated Reprogramming of Mouse Embryonic Fibroblasts

Published on: March 22, 2017

7.5K
Live Imaging Followed by Single Cell Tracking to Monitor Cell Biology and the Lineage Progression of Multiple Neural Populations
10:55

Live Imaging Followed by Single Cell Tracking to Monitor Cell Biology and the Lineage Progression of Multiple Neural Populations

Published on: December 16, 2017

8.7K

结论:

  • Ascl1具有比以前理解的更广泛的谱系重编程潜力.
  • Ascl1可以作为多个细胞命运转换的主调节器.
  • 这些发现为再生医学中治疗性细胞生成开辟了新的可能性.