Lineage contribution of the mesendoderm progenitors in the gastrulating mouse embryo

IF 8.7 1区 生物学 Q1 CELL BIOLOGY Developmental cell Pub Date : 2025-03-24 DOI:10.1016/j.devcel.2025.02.015
V. Pragathi Masamsetti, Nazmus Salehin, Hani Jieun Kim, Nicole Santucci, Megan Weatherstone, Riley McMahon, Lee L. Marshall, Hilary Knowles, Jane Sun, Josh B. Studdert, Nader Aryamanesh, Ran Wang, Naihe Jing, Pengyi Yang, Pierre Osteil, Patrick P.L. Tam
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Abstract

A population of putative mesendoderm progenitors that can contribute cellular descendants to both mesoderm and endoderm lineages is identified in the gastrulating mouse embryo. These progenitor cells are localized to the posterior epiblast, primitive streak, and nascent mesoderm of mid-streak- (E7.0) to late-streak-stage (E7.5) embryos. Lineage tracing in vivo identified that putative mesendoderm progenitors contribute descendants to the definitive endoderm and the axial mesendoderm of E7.75 embryos and to the endoderm of the foregut and hindgut of the E8.5–8.75 embryos. Differentiation of mouse epiblast stem cells identified that the choice between endoderm and mesoderm cell fates depends on the timing of Mixl1 activation upon exit from pluripotency. The knowledge gained on the spatiotemporal distribution of mesendoderm progenitors and the molecular drivers underpinning the divergence of cell lineages in these progenitors enriches our mechanistic understanding of the allocation of the tissue progenitors to germ layer derivatives in early development.

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小鼠原肠泌胚中中胚层祖细胞的谱系贡献
在原肠泌乳小鼠胚胎中发现了一个假定的中胚层祖细胞群体,它可以为中胚层和内胚层谱系贡献细胞后代。这些祖细胞定位于中纹期(E7.0)到晚纹期(E7.5)胚胎的后外胚层、原始条纹和新生中胚层。体内谱系追踪发现,假定的中胚层祖细胞为E7.75胚胎的终胚层和轴胚层以及E8.5-8.75胚胎的前肠和后肠胚层提供后代。小鼠外胚层干细胞的分化表明,内胚层和中胚层细胞命运的选择取决于多能性退出时Mixl1激活的时机。关于中胚层祖细胞的时空分布和支持这些祖细胞谱系分化的分子驱动因素的知识丰富了我们对早期发育中组织祖细胞向胚层衍生物分配的机制理解。
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来源期刊
Developmental cell
Developmental cell 生物-发育生物学
CiteScore
18.90
自引率
1.70%
发文量
203
审稿时长
3-6 weeks
期刊介绍: Developmental Cell, established in 2001, is a comprehensive journal that explores a wide range of topics in cell and developmental biology. Our publication encompasses work across various disciplines within biology, with a particular emphasis on investigating the intersections between cell biology, developmental biology, and other related fields. Our primary objective is to present research conducted through a cell biological perspective, addressing the essential mechanisms governing cell function, cellular interactions, and responses to the environment. Moreover, we focus on understanding the collective behavior of cells, culminating in the formation of tissues, organs, and whole organisms, while also investigating the consequences of any malfunctions in these intricate processes.
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