Zhang Xiaoyu, Li Zizhang, Chen Jingyu, Yang Wenjing, He Xingxing, Wu Peng, Chen Feng, Zhou Ziwei, Ren Chenze, Shan Yuyan, Wen Xiewen, Lyubetsky Vassily A, Rusin Leonid Yu, Chen Xiaoshu, Yang Jian-Rong
Advanced Medical Technology Center, The First Affiliated Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.
Department of Genetics and Biomedical Informatics, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China.
Adv Sci (Weinh). 2025 Aug;12(30):e2406208. doi: 10.1002/advs.202406208. Epub 2025 Apr 30.
Robust development is essential for multicellular organisms. While various mechanisms contributing to developmental robustness are identified at the subcellular level, those at the intercellular and tissue level remain underexplored. This question is approached using a well-established in vitro directed differentiation model recapitulating the in vivo development of lung progenitor cells from human embryonic stem cells. An integrated analysis of high-density cell lineage trees (CLTs) and single-cell transcriptomes of differentiating colonies enabled the resolution of known cell types and developmental hierarchies. This dataset showed little support for the contribution of transcriptional memory to developmental robustness. Nevertheless, stable terminal cell type compositions are observed among many subclones, which enhances developmental robustness because the colony can retain a relatively stable composition even if some subclones are abolished by cell death. Furthermore, it is found that many subclones are formed by sub-CLTs resembling each other in terms of both terminal cell type compositions and topological structures. The presence of stereotyped sub-CLTs constitutes a novel basis for developmental robustness. Moreover, these results suggest a unique perspective on individual cells' function in the context of stereotyped sub-CLTs, which can bridge the knowledge of the atlas of cell types and how they are organized into functional tissues.
稳健的发育对于多细胞生物至关重要。虽然在亚细胞水平上已经确定了多种有助于发育稳健性的机制,但细胞间和组织水平上的机制仍未得到充分探索。我们使用一个成熟的体外定向分化模型来解决这个问题,该模型概括了人胚胎干细胞在体内肺祖细胞的发育过程。对分化菌落的高密度细胞谱系树(CLTs)和单细胞转录组进行综合分析,能够解析已知的细胞类型和发育层次结构。该数据集几乎没有支持转录记忆对发育稳健性的贡献。然而,在许多亚克隆中观察到稳定的终末细胞类型组成,这增强了发育稳健性,因为即使一些亚克隆因细胞死亡而被消除,菌落仍能保持相对稳定的组成。此外,发现许多亚克隆是由在终末细胞类型组成和拓扑结构方面彼此相似的亚CLTs形成的。定型亚CLTs的存在构成了发育稳健性的一个新基础。此外,这些结果为定型亚CLTs背景下单个细胞的功能提供了独特的视角,这可以弥合细胞类型图谱及其如何组织成功能组织的知识。