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控制肺肺泡出现的基因组学、表观基因组学和生物物理线索。

Genomic, epigenomic, and biophysical cues controlling the emergence of the lung alveolus.

机构信息

Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Penn-CHOP Lung Biology Institute, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Science. 2021 Mar 12;371(6534). doi: 10.1126/science.abc3172.

Abstract

The lung alveolus is the functional unit of the respiratory system required for gas exchange. During the transition to air breathing at birth, biophysical forces are thought to shape the emerging tissue niche. However, the intercellular signaling that drives these processes remains poorly understood. Applying a multimodal approach, we identified alveolar type 1 (AT1) epithelial cells as a distinct signaling hub. Lineage tracing demonstrates that AT1 progenitors align with receptive, force-exerting myofibroblasts in a spatial and temporal manner. Through single-cell chromatin accessibility and pathway expression (SCAPE) analysis, we demonstrate that AT1-restricted ligands are required for myofibroblasts and alveolar formation. These studies show that the alignment of cell fates, mediated by biophysical and AT1-derived paracrine signals, drives the extensive tissue remodeling required for postnatal respiration.

摘要

肺气泡是呼吸系统进行气体交换的功能单位。在出生时向空气呼吸的转变过程中,生物物理力被认为可以塑造新兴的组织生态位。然而,驱动这些过程的细胞间信号仍然知之甚少。通过应用多模态方法,我们确定了肺泡 I 型(AT1)上皮细胞作为一个独特的信号枢纽。谱系追踪表明,AT1 祖细胞以时空方式与接受、施加力的肌成纤维细胞对齐。通过单细胞染色质可及性和通路表达(SCAPE)分析,我们证明了肌成纤维细胞和肺泡形成所需的 AT1 限制配体。这些研究表明,由生物物理和 AT1 衍生的旁分泌信号介导的细胞命运对齐,驱动了出生后呼吸所需的广泛组织重塑。

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