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用于研究人肺细胞外基质和成纤维细胞功能的 3D 体外水凝胶模型。

3D in vitro hydrogel models to study the human lung extracellular matrix and fibroblast function.

机构信息

Department of Biology, Okanagan Campus, University of British Columbia, 3187 University Way, ASC366, Kelowna, BC, V1V1V7, Canada.

Centre for Heart Lung Innovation, St. Paul's Hospital, Vancouver, BC, V6Z 1Y6, Canada.

出版信息

Respir Res. 2023 Oct 5;24(1):242. doi: 10.1186/s12931-023-02548-6.

Abstract

The pulmonary extracellular matrix (ECM) is a macromolecular structure that provides mechanical support, stability and elastic recoil for different pulmonary cells including the lung fibroblasts. The ECM plays an important role in lung development, remodeling, repair, and the maintenance of tissue homeostasis. Biomechanical and biochemical signals produced by the ECM regulate the phenotype and function of various cells including fibroblasts in the lungs. Fibroblasts are important lung structural cells responsible for the production and repair of different ECM proteins (e.g., collagen and fibronectin). During lung injury and in chronic lung diseases such as asthma, idiopathic pulmonary fibrosis (IPF) and chronic obstructive pulmonary disease (COPD), an abnormal feedback between fibroblasts and the altered ECM disrupts tissue homeostasis and leads to a vicious cycle of fibrotic changes resulting in tissue remodeling. In line with this, using 3D hydrogel culture models with embedded lung fibroblasts have enabled the assessment of the various mechanisms involved in driving defective (fibrotic) fibroblast function in the lung's 3D ECM environment. In this review, we provide a summary of various studies that used these 3D hydrogel models to assess the regulation of the ECM on lung fibroblast phenotype and function in altered lung ECM homeostasis in health and in chronic respiratory disease.

摘要

肺细胞外基质(ECM)是一种提供机械支撑、稳定性和弹性回复的高分子结构,为包括肺成纤维细胞在内的不同肺细胞提供支持。ECM 在肺发育、重塑、修复和组织内稳态维持中发挥着重要作用。ECM 产生的生物力学和生化信号调节着各种细胞的表型和功能,包括肺中的成纤维细胞。成纤维细胞是重要的肺结构细胞,负责产生和修复不同的 ECM 蛋白(如胶原蛋白和纤维连接蛋白)。在肺损伤和哮喘、特发性肺纤维化(IPF)和慢性阻塞性肺疾病(COPD)等慢性肺部疾病中,成纤维细胞和改变的 ECM 之间的异常反馈破坏了组织内稳态,并导致纤维化变化的恶性循环,导致组织重塑。基于此,使用嵌入肺成纤维细胞的 3D 水凝胶培养模型,使人们能够评估在 3D ECM 环境中驱动肺成纤维细胞功能缺陷(纤维化)的各种机制。在这篇综述中,我们总结了使用这些 3D 水凝胶模型评估 ECM 对肺成纤维细胞表型和功能的调节,以及在健康和慢性呼吸道疾病中改变的肺 ECM 内稳态下的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a632/10552248/8030e9b69fbb/12931_2023_2548_Fig1_HTML.jpg

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