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Epigenetic Signatures and Plasticity of Intestinal and Other Stem Cells
Annual Review of Physiology ( IF 18.2 ) Pub Date : 2021-02-10 , DOI: 10.1146/annurev-physiol-021119-034520
Madhurima Saxena 1, 2, 3 , Ramesh A Shivdasani 1, 2, 4
Affiliation  

The cardinal properties of adult tissue stem cells are self-renewal and the ability to generate diverse resident cell types. The daily losses of terminally differentiated intestinal, skin, and blood cells require “professional” stem cells to produce replacements. This occurs by continuous expansion of stem cells and their immediate progeny, followed by coordinated activation of divergent transcriptional programs to generate stable cells with diverse functions. Other tissues turn over slowly, if at all, and vary widely in strategies for facultative stem cell activity or interconversion among mature resident cell types (transdifferentiation). Cell fate potential is programmed in tissue-specific configurations of chromatin, which restrict the complement of available genes and cis-regulatory elements, hence allowing specific cell types to arise. Using as a model the transcriptional and chromatin basis of cell differentiation and dedifferentiation in intestinal crypts, we discuss here how self-renewing and other tissues execute homeostatic and injury-responsive stem cell activity.

中文翻译:


肠道和其他干细胞的表观遗传特征和可塑性

成体组织干细胞的主要特性是自我更新和产生不同常驻细胞类型的能力。终末分化的肠道、皮肤和血细胞每天都在流失,需要“专业”干细胞来产生替代品。这是通过干细胞及其直接后代的持续扩增,然后协同激活不同的转录程序来产生具有不同功能的稳定细胞而发生的。其他组织的转换速度很慢,如果有的话,并且在兼性干细胞活性或成熟常驻细胞类型之间的相互转化(转分化)策略方面差异很大。细胞命运潜能在染色质的组织特异性结构中被编程,这限制了可用基因和顺式的补充调节元件,从而允许出现特定的细胞类型。我们以肠隐窝中细胞分化和去分化的转录和染色质基础为模型,在此讨论自我更新和其他组织如何执行稳态和损伤反应性干细胞活动。

更新日期:2021-02-11
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