Spatial Transcriptomics Unveils the Blueprint of Mammalian Lung Development.

IF 7.9
Mingyue Chen 陈明月, Junjie Lv 吕俊杰, Qiao Zhang 张乔, Qian Gong 龚倩, Ting Zhao 赵婷, Zhenping Chen 陈振平, Haishen Xu 徐海深, Nan Zhou 周南, Shan Jiang 姜姗, Jian Du 都建, Xuepeng Chen 陈雪鹏, Yuwen Ke 柯玉文
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Abstract

Mammalian lung development is a complex, highly orchestrated process involving the precise coordination of diverse cell types. Despite significant advances, the spatial gene expression patterns and regulatory mechanisms within the developmental niches of different lung structures remain incompletely understood. In this study, we present a comprehensive spatial transcriptomic atlas of mouse lung development, spanning from the early pseudoglandular to the alveolar stage. We further uncover transcription factor (TF) regulation landscapes by integrating spatial epigenome, including novel TF-enhancer-driven regulons (eRegulons) critical for epithelial progenitors during early lung development. Our analysis also identifies hundreds of spatiotemporally dynamic cell-cell communications, such as BMP8B-mediated ligand-receptor signaling enriched in airway branching. Notably, we delineate the distinct developmental trajectories of alveolar AT1 and AT2 cells and reveal that collagen pathways facilitate their spatial convergence, forming primary alveoli during the canalicular-saccular transition. Together, this spatial transcriptomic atlas provides a foundational resource for understanding the complex cellular and molecular orchestration underlying mammalian lung development.

空间转录组学揭示了哺乳动物肺发育的蓝图。
哺乳动物肺的发育是一个复杂的、高度协调的过程,涉及多种细胞类型的精确协调。尽管取得了重大进展,但不同肺结构发育生态位内的空间基因表达模式和调控机制仍不完全清楚。在这项研究中,我们展示了从早期假腺到肺泡期小鼠肺发育的全面空间转录组图谱。我们通过整合空间表观基因组进一步揭示转录因子(TF)调控景观,包括在早期肺发育过程中对上皮祖细胞至关重要的新型TF增强子驱动调控(eregons)。我们的分析还确定了数百种时空动态的细胞-细胞通信,如bmp8b介导的配体受体信号在气道分支中富集。值得注意的是,我们描绘了肺泡AT1和AT2细胞的不同发育轨迹,并揭示了胶原通路促进它们的空间收敛,在小管-囊状过渡期间形成初级肺泡。总之,这个空间转录组图谱为理解哺乳动物肺发育背后复杂的细胞和分子协调提供了基础资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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