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相关概念视频

Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

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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...
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Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

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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...
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Introduction to Nuclear Reprogramming01:14

Introduction to Nuclear Reprogramming

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Nuclear reprogramming is the process of switching gene expression of one cell type to that of another cell type, usually from a differentiated cell state to an undifferentiated cell state. Differentiation occurs during processes such as development and morphogenesis, tissue regeneration, and malignancy. Cells can also be artificially induced to reprogram their gene expression by techniques such as nuclear transfer, induced pluripotency, and cell fusion. Such techniques have many applications in...
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Forced Transdifferentiation01:28

Forced Transdifferentiation

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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...
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相关实验视频

Updated: Mar 30, 2026

Induced Pluripotent Stem Cell Generation from Blood Cells Using Sendai Virus and Centrifugation
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Induced Pluripotent Stem Cell Generation from Blood Cells Using Sendai Virus and Centrifugation

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直接细胞重编程是一种随机过程,易于加速加速.

Jacob Hanna1, Krishanu Saha, Bernardo Pando

  • 1The Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA. Hanna@wi.mit.edu

Nature
|November 10, 2009
PubMed
概括
此摘要是机器生成的。

将体细胞重新编程为诱导多能干细胞 (iPS) 是一个持续的过程. 细胞分裂率和纳米人影响重编程速度,突出显示细胞分裂是表观遗传变化的关键.

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Kinetic Measurement and Real Time Visualization of Somatic Reprogramming
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Induced Pluripotent Stem Cell Generation from Blood Cells Using Sendai Virus and Centrifugation
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Induced Pluripotent Stem Cell Generation from Blood Cells Using Sendai Virus and Centrifugation

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Kinetic Measurement and Real Time Visualization of Somatic Reprogramming
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科学领域:

  • 干细胞生物学 干细胞生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
  • 分子生物学分子生物学

背景情况:

  • 将体细胞直接重新编程成诱导多能干细胞 (iPS) 通常通过过度表达Oct4,Sox2,Klf4和c-Myc来实现.
  • 然而,只有一小部分体细胞成功地经历了重编程.

研究的目的:

  • 研究重编程过程背后的动力学和机制.
  • 确定影响诱导多能诱导效率和速度的因素.

主要方法:

  • 在小鼠体细胞中,重编程因子 (Oct4,Sox2,Klf4,c-Myc) 的过度表达.
  • 抑制了p53/p21通路的发生.
  • 过度表达的Lin28和纳米.
  • 重编程动力学和细胞增殖率的定量分析.

主要成果:

  • 重编程是一种持续的随机过程,大多数细胞在持续表达和生长后最终成为iPS细胞.
  • 抑制p53/p21或Lin28过度表达加速了iPS细胞的形成,与细胞分裂率的增加成比例.
  • 纳米细胞过度表达加速了细胞分裂速度独立的重编程.
  • 确定了不同的细胞分裂速度依赖和独立的重编程加速模式.

结论:

  • 细胞分裂的数量是推动表观遗传重编程到多能性的关键参数.
  • 细胞增殖率和像纳诺基这样的特定因素都在调节重编程动力学方面发挥着重要作用.