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肺泡干细胞的多顶端极性及其在肺发育和再生过程中的动态变化。

Multi-apical polarity of alveolar stem cells and their dynamics during lung development and regeneration.

作者信息

Konkimalla Arvind, Konishi Satoshi, Kobayashi Yoshihiko, Kadur Lakshminarasimha Murthy Preetish, Macadlo Lauren, Mukherjee Ananya, Elmore Zachary, Kim So-Jin, Pendergast Ann Marie, Lee Patty J, Asokan Aravind, Knudsen Lars, Bravo-Cordero Jose Javier, Tata Aleksandra, Tata Purushothama Rao

机构信息

Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.

Medical Scientist Training Program, Duke University School of Medicine, Durham, NC 27710, USA.

出版信息

iScience. 2022 Sep 12;25(10):105114. doi: 10.1016/j.isci.2022.105114. eCollection 2022 Oct 21.

Abstract

Epithelial cells of diverse tissues are characterized by the presence of a single apical domain. In the lung, electron microscopy studies have suggested that alveolar type-2 epithelial cells (AT2s) en face multiple alveolar sacs. However, apical and basolateral organization of the AT2s and their establishment during development and remodeling after injury repair remain unknown. Thick tissue imaging and electron microscopy revealed that a single AT2 can have multiple apical domains that enface multiple alveoli. AT2s gradually establish multi-apical domains post-natally, and they are maintained throughout life. Lineage tracing, live imaging, and selective cell ablation revealed that AT2s dynamically reorganize multi-apical domains during injury repair. Single-cell transcriptome signatures of residual AT2s revealed changes in cytoskeleton and cell migration. Significantly, cigarette smoke and oncogene activation lead to dysregulation of multi-apical domains. We propose that the multi-apical domains of AT2s enable them to be poised to support the regeneration of a large array of alveolar sacs.

摘要

多种组织的上皮细胞的特征是存在单个顶端结构域。在肺部,电子显微镜研究表明,II型肺泡上皮细胞(AT2)面向多个肺泡囊。然而,AT2的顶端和基底外侧组织及其在发育过程中的建立以及损伤修复后的重塑情况仍不清楚。厚组织成像和电子显微镜显示,单个AT2可以有多个面向多个肺泡的顶端结构域。AT2在出生后逐渐建立多顶端结构域,并在整个生命过程中保持。谱系追踪、实时成像和选择性细胞消融显示,AT2在损伤修复过程中动态重组多顶端结构域。残留AT2的单细胞转录组特征揭示了细胞骨架和细胞迁移的变化。值得注意的是,香烟烟雾和癌基因激活会导致多顶端结构域的失调。我们提出,AT2的多顶端结构域使它们能够随时准备支持大量肺泡囊的再生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3ff/9519774/48fdadc79c5e/fx1.jpg

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