通过破坏表观遗传障碍,将嗅觉源细胞转化为具有干细胞特征的细胞
bioRxiv : the preprint server for biology
|May 15, 2024
概括
在嗅觉神经元细胞中扰乱Ehmt2染色质修饰剂诱导干细胞特征. 这表明嗅觉谱系内固有的可塑性,为再生和重编程提供了洞察力.
科学领域:
- 神经科学是一个神经科学.
- 细胞生物学 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.
背景情况:
- 哺乳动物的嗅觉神经元系是再生的.
- 多能细胞补充嗅觉感官神经元和其他细胞类型.
- 早期的细胞可以去分化,以帮助组织在受伤后修复.
研究的目的:
- 探索嗅觉感官神经系细胞的可塑性.
- 研究表观遗传修饰对嗅觉细胞可塑性的影响.
主要方法:
- 使用两种来自嗅觉斑点的细胞系,模拟不成熟的嗅觉感官神经元阶段.
- 扰乱了Ehmt2的染色体修饰器.
- 评估了生长特性,形态和基因表达的变化.
主要成果:
- 埃姆特2扰动改变了细胞,使其具有干细胞特征.
- 这种转变取决于大T抗原表达.
- 过度表达Sox2增强了类似干细胞的转化.
结论:
- 表观遗传修饰影响嗅觉神经元谱系的可塑性.
- 这些发现提供了关于嗅觉细胞的再生潜力和细胞重编程的见解.
相关概念视频
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 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
Induced Pluripotent Stem Cells
4.0K
Stem cells are undifferentiated cells that divide and produce different cell types. Ordinarily, cells that have differentiated into a specific cell type are terminally differentiated; however, scientists have found a way to reprogram these mature cells so that they dedifferentiate and return to an unspecialized, proliferative state. These cells are pluripotent like embryonic stem cells—able to produce all cell types—and are called induced pluripotent stem cells (iPSCs).
Somatic...
Somatic...
4.0K
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
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


