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在缺乏Pdzk1的情况下捕获小鼠胚胎干细胞的全能性

Capture of Totipotency in Mouse Embryonic Stem Cells in the Absence of Pdzk1.

作者信息

Zhang Wenhao, Zhao Yiding, Yang Zhe, Yan Jing, Wang Haisong, Nie Shaochen, Jia Qingshen, Ding Dan, Tong Chao, Zhang Xiao-Ou, Gao Qian, Shuai Ling

机构信息

State Key Laboratory of Medicinal Chemical Biology and College of Pharmacy, Nankai Animal Resources Center and Reproductive Regulation, Institute of Transplantation Medicine, Nankai University, Tianjin, 300350, China.

Shanghai Key Laboratory of Maternal and Fetal Medicine, Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Frontier Science Center for Stem Cell Research, School of Life and Science and Technology, Tongji University, Shanghai, 200092, China.

出版信息

Adv Sci (Weinh). 2025 Feb;12(6):e2408852. doi: 10.1002/advs.202408852. Epub 2024 Dec 4.

Abstract

Totipotent cells can differentiate into three lineages: the epiblast, primitive endoderm, and trophectoderm. Naturally, only early fertilized embryos possess totipotency, and they lose this ability as they develop. The expansion of stem cell differentiation potential has been a hot topic in developmental biology for years, particularly with respect to the generation totipotent-like stem cells. Here, the study describes the establishment of totipotency in embryonic stem cells (ESCs) via the deletion of a single gene, Pdzk1. Pdzk1-knockout (KO) ESCs substantially contribute to the fetus, placenta, and yolk sac in chimera assays but can also self-organize to form standard blastocyst-like structures containing the three lineages efficiently; thus, they exhibit full developmental potential as early blastomeres. Single-cell transcriptome and bulk RNA-seq comprehensive analyses revealed that Pdzk1-KO activates several lineage inducers (C1qa, C1qb, Fgf5, and Cdx2) to break down barriers between embryonic and extraembryonic tissues, making these lineages switch smoothly and resulting in a totipotent-like state. This versatile and scalable system provides a robust experimental model for differentiation potency and cell fate studies.

摘要

全能细胞可分化为三个谱系

上胚层、原始内胚层和滋养外胚层。自然情况下,只有早期受精胚胎具有全能性,并且它们在发育过程中会失去这种能力。多年来,干细胞分化潜能的扩展一直是发育生物学中的热门话题,尤其是在生成类全能干细胞方面。在此,该研究描述了通过删除单个基因Pdzk1在胚胎干细胞(ESC)中建立全能性。在嵌合体实验中,Pdzk1基因敲除(KO)的ESC对胎儿、胎盘和卵黄囊有显著贡献,但也能自我组织形成高效包含这三个谱系的标准囊胚样结构;因此,它们表现出与早期卵裂球一样的完全发育潜能。单细胞转录组和大量RNA测序综合分析表明,Pdzk1基因敲除激活了几种谱系诱导因子(C1qa、C1qb、Fgf5和Cdx2),以打破胚胎组织和胚外组织之间的屏障,使这些谱系顺利转换并导致类全能状态。这个通用且可扩展的系统为分化潜能和细胞命运研究提供了一个强大的实验模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db2e/11809344/17252547b0fe/ADVS-12-2408852-g008.jpg

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