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哺乳动物原肠胚形成过程中细胞多能性和命运决定的表观遗传控制。

Epigenetic Control of Cell Potency and Fate Determination during Mammalian Gastrulation.

机构信息

Quantitative Stem Cell Biology Lab, Francis Crick Institute, London NW1 1AT, UK.

Adelaide Centre for Epigenetics, School of Biomedicine, Faculty of Health and Medical Sciences, University of Adelaide, Adelaide 5000, Australia.

出版信息

Genes (Basel). 2023 May 25;14(6):1143. doi: 10.3390/genes14061143.

Abstract

Pluripotent embryonic stem cells have a unique and characteristic epigenetic profile, which is critical for differentiation to all embryonic germ lineages. When stem cells exit the pluripotent state and commit to lineage-specific identities during the process of gastrulation in early embryogenesis, extensive epigenetic remodelling mediates both the switch in cellular programme and the loss of potential to adopt alternative lineage programmes. However, it remains to be understood how the stem cell epigenetic profile encodes pluripotency, or how dynamic epigenetic regulation helps to direct cell fate specification. Recent advances in stem cell culture techniques, cellular reprogramming, and single-cell technologies that can quantitatively profile epigenetic marks have led to significant insights into these questions, which are important for understanding both embryonic development and cell fate engineering. This review provides an overview of key concepts and highlights exciting new advances in the field.

摘要

多能胚胎干细胞具有独特而特征性的表观遗传特征,这对于分化为所有胚胎生殖系至关重要。当干细胞退出多能状态并在早期胚胎发生的原肠胚形成过程中特化到特定谱系身份时,广泛的表观遗传重塑介导细胞程序的转变和丧失采用替代谱系程序的潜力。然而,目前尚不清楚干细胞的表观遗传特征如何编码多能性,或者动态表观遗传调控如何有助于指导细胞命运特化。最近在干细胞培养技术、细胞重编程和能够定量分析表观遗传标记的单细胞技术方面的进展,为这些问题提供了重要的见解,这些问题对于理解胚胎发育和细胞命运工程都很重要。本文综述了该领域的关键概念,并重点介绍了令人兴奋的新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceb1/10298296/25562cead19c/genes-14-01143-g001.jpg

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