适应性金属离子运输和金属调节驱动的分化在多能合成细胞中的多能合成细胞
Sayuri L Higashi1,2,3,4, Yanjun Zheng1, Taniya Chakraborty1
1Institute of Physiological Chemistry and Pathobiochemistry, University of Münster, Münster, Germany.
Nature chemistry
|December 23, 2024
概括
合成细胞通过休眠酶和连续的金属离子输送来实现多能性. 这种受控的分化过程允许合成细胞根据离子体添加的顺序发展成不同的细胞命运.
科学领域:
- 合成生物学 合成生物学
- 生物化学 生化学
- 细胞分化 细胞分化
背景情况:
- 多能细胞根据顺序信号分化成各种细胞类型.
- 在合成系统中理解和复制细胞分化是一个关键的挑战.
研究的目的:
- 在合成细胞中实现多能性.
- 为了控制合成细胞的分化,使用连续的金属离子运输.
- 探索合成细胞对有序刺激的记忆和反应.
主要方法:
- 将三个休眠的阿波金属酶纳入巨型单状囊泡 (GUVs).
- 选择性运输金属离子辅助因子进入GUV使用离子体.
- 原子模拟用于研究GUV膜内的离子体相互作用.
- 连续添加离子体以观察差异化路径.
主要成果:
- 多能GUVs根据离子体添加的序列分化为不同的命运.
- 第一次离子体添加引发了特定的反应:pH值升高,过氧化的产生,或GUV溶解.
- 随后的离子体添加引起了减弱的反应,表明一种细胞记忆形式.
- 根据加法序列,GUVs可以分为五种不同的最终命运.
结论:
- 连续的金属离子运输可以在合成细胞中编程分化途径.
- 合成细胞系统表现出以前离子体相互作用的记忆.
- 这项工作为创造复杂的合成细胞行为和分化提供了一个新的平台.
更多相关视频
11:38Author Spotlight: Enhancing PSC-to-Functional Cell Differentiation Using ML Models Based on Live-Cell Bright-Field Imaging
Published on: October 4, 2024
485
14:37Directed Differentiation of Primitive and Definitive Hematopoietic Progenitors from Human Pluripotent Stem Cells
Published on: November 1, 2017
10.9K
相关概念视频
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...
Artificial...
1.9K
iPS Cell Differentiation
2.6K
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.
2.6K
Chromatin Modification in iPS Cells
1.6K
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...
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...
1.6K
