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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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Chromatin Modification in iPS Cells01:32

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
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Forced Transdifferentiation01:28

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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: May 27, 2025

Reprograming Model of Human Monocyte-derived Macrophages for In-vitro Assays
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Reprograming Model of Human Monocyte-derived Macrophages for In-vitro Assays

Published on: April 18, 2025

153

代谢重编程塑造了巨细胞的翻译后修饰.

Ziyi Han1, Yinhao Shen1, Yuqi Yan2

  • 1State Key Laboratory of Swine and Poultry Breeding Industry, College of Animal Science, South China Agricultural University, Guangzhou, 510642, China.

Molecular aspects of medicine
|February 20, 2025
PubMed
概括

巨细胞重编程新陈代谢和翻译后修饰 (PTMs),以响应刺激并改变功能. 改变的代谢物,包括葡萄糖,脂质和氨基酸,通过PTMs对巨细胞两极分化产生关键影响.

关键词:
这是天生的免疫力.巨细胞是一个巨细胞.代谢重编程是一种代谢重编程.后翻译修改后的修改.

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Metabolic Characterization of Polarized M1 and M2 Bone Marrow-derived Macrophages Using Real-time Extracellular Flux Analysis
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Analyzing Ex Vivo Metabolic Flux in Splenic and Cardiac Macrophages and Bone Marrow Monocytes
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相关实验视频

Last Updated: May 27, 2025

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Reprograming Model of Human Monocyte-derived Macrophages for In-vitro Assays

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Metabolic Characterization of Polarized M1 and M2 Bone Marrow-derived Macrophages Using Real-time Extracellular Flux Analysis
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Metabolic Characterization of Polarized M1 and M2 Bone Marrow-derived Macrophages Using Real-time Extracellular Flux Analysis

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Analyzing Ex Vivo Metabolic Flux in Splenic and Cardiac Macrophages and Bone Marrow Monocytes
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175

科学领域:

  • 免疫学 免疫学 免疫学
  • 代谢途径 代谢途径
  • 细胞生物学 细胞生物学

背景情况:

  • 巨细胞是关键的免疫细胞,分化成不同的表型.
  • 这种两极分化涉及显著的代谢和表观遗传变化.
  • 翻译后修饰 (PTMs) 对于调节巨细胞功能至关重要.

研究的目的:

  • 审查改变的代谢物如何影响巨细胞两极分化.
  • 检查PTMs在巨细胞代谢重编程中的作用.
  • 了解代谢物驱动的PTMs对巨相关疾病的影响.

主要方法:

  • 关于巨细胞两极分化研究的文献综述.
  • 分析巨细胞中的代谢途径 (葡萄糖,脂质,氨基酸).
  • 在巨细胞极化中的表观遗传和PTM的检查.

主要成果:

  • 代谢重编程,包括葡萄糖,脂质和氨基酸代谢的变化,是巨细胞两极分化的核心.
  • 动态PTMs是由微环境代谢物调节的,决定了巨细胞的反应.
  • 异常代谢物及其PTM作用有助于巨相关疾病的疾病进展.

结论:

  • 代谢物在极化过程中通过PTMs显著塑造巨细胞信号和代谢.
  • 了解这些代谢物-PTM相互作用对于向疾病中的巨细胞功能至关重要.