Guan Guoye, Li Zelin, Ma Yiming, Ye Pohao, Cao Jianfeng, Wong Ming-Kin, Ho Vincy Wing Sze, Chan Lu-Yan, Yan Hong, Tang Chao, Zhao Zhongying
Center for Quantitative Biology, Peking University, Beijing, China.
Department of Systems Biology, Harvard Medical School, Boston, MA, USA.
Nat Commun. 2025 Apr 18;16(1):3700. doi: 10.1038/s41467-025-58878-0.
How cells change shape is crucial for the development of tissues, organs and embryos. However, studying these shape changes in detail is challenging. Here we present a comprehensive real-time cellular map that covers over 95% of the cells formed during Caenorhabditis elegans embryogenesis, featuring nearly 400,000 3D cell regions. This map includes information on each cell's identity, lineage, fate, shape, volume, surface area, contact area, and gene expression profiles, all accessible through our user-friendly software and website. Our map allows for detailed analysis of key developmental processes, including dorsal intercalation, intestinal formation, and muscle assembly. We show how Notch and Wnt signaling pathways, along with mechanical forces from cell interactions, regulate cell fate decisions and size asymmetries. Our findings suggest that repeated Notch signaling drives size disparities in the large excretory cell, which functions like a kidney. This work sets the stage for in-depth studies of the mechanisms controlling cell fate differentiation and morphogenesis.
细胞如何改变形状对于组织、器官和胚胎的发育至关重要。然而,详细研究这些形状变化具有挑战性。在这里,我们展示了一个全面的实时细胞图谱,该图谱涵盖了秀丽隐杆线虫胚胎发育过程中形成的超过95%的细胞,具有近40万个三维细胞区域。该图谱包括每个细胞的身份、谱系、命运、形状、体积、表面积、接触面积和基因表达谱等信息,所有这些都可以通过我们用户友好的软件和网站获取。我们的图谱允许对关键发育过程进行详细分析,包括背侧插入、肠道形成和肌肉组装。我们展示了Notch和Wnt信号通路以及细胞相互作用产生的机械力如何调节细胞命运决定和大小不对称性。我们的研究结果表明,重复的Notch信号驱动大型排泄细胞(其功能类似于肾脏)的大小差异。这项工作为深入研究控制细胞命运分化和形态发生的机制奠定了基础。