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肺上皮干细胞及微环境在肺泡再生与疾病中的作用

Epithelial stem cells and niches in lung alveolar regeneration and diseases.

作者信息

Zhang Jilei, Liu Yuru

机构信息

Department of Pharmacology and Regenerative Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.

University of Illinois Cancer Center, Chicago, IL 60612, USA.

出版信息

Chin Med J Pulm Crit Care Med. 2024 Mar;2(1):17-26. doi: 10.1016/j.pccm.2023.10.007. Epub 2024 Feb 8.

Abstract

Alveoli serve as the functional units of the lungs, responsible for the critical task of blood-gas exchange. Comprising type I (AT1) and type II (AT2) cells, the alveolar epithelium is continuously subject to external aggressors like pathogens and airborne particles. As such, preserving lung function requires both the homeostatic renewal and reparative regeneration of this epithelial layer. Dysfunctions in these processes contribute to various lung diseases. Recent research has pinpointed specific cell subgroups that act as potential stem or progenitor cells for the alveolar epithelium during both homeostasis and regeneration. Additionally, endothelial cells, fibroblasts, and immune cells synergistically establish a nurturing microenvironment-or "niche"-that modulates these epithelial stem cells. This review aims to consolidate the latest findings on the identities of these stem cells and the components of their niche, as well as the molecular mechanisms that govern them. Additionally, this article highlights diseases that arise due to perturbations in stem cell-niche interactions. We also discuss recent technical innovations that have catalyzed these discoveries. Specifically, this review underscores the heterogeneity, plasticity, and dynamic regulation of these stem cell-niche systems. It is our aspiration that a deeper understanding of the fundamental cellular and molecular mechanisms underlying alveolar homeostasis and regeneration will open avenues for identifying novel therapeutic targets for conditions such as chronic obstructive pulmonary disease (COPD), fibrosis, coronavirus disease 2019 (COVID-19), and lung cancer.

摘要

肺泡作为肺的功能单位,负责血液与气体交换这一关键任务。肺泡上皮由I型(AT1)和II型(AT2)细胞组成,不断受到病原体和空气传播颗粒等外部侵害。因此,维持肺功能需要该上皮层的稳态更新和修复性再生。这些过程中的功能障碍会导致各种肺部疾病。最近的研究已经确定了在稳态和再生过程中作为肺泡上皮潜在干细胞或祖细胞的特定细胞亚群。此外,内皮细胞、成纤维细胞和免疫细胞协同建立一个滋养性微环境——即“生态位”——来调节这些上皮干细胞。本综述旨在整合关于这些干细胞的身份、其生态位的组成成分以及调控它们的分子机制的最新研究结果。此外,本文还重点介绍了由于干细胞与生态位相互作用受到干扰而引发的疾病。我们还讨论了促成这些发现的近期技术创新。具体而言,本综述强调了这些干细胞 - 生态位系统的异质性、可塑性和动态调控。我们期望,对肺泡稳态和再生背后的基本细胞和分子机制有更深入的了解,将为识别慢性阻塞性肺疾病(COPD)、纤维化、2019冠状病毒病(COVID - 19)和肺癌等疾病的新型治疗靶点开辟道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b90d/11332828/8defc8774ddb/gr1.jpg

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