机械生物学
纤维化
细胞外基质
医学
肺病
肺
吡非尼酮
特发性肺纤维化
疾病
肺纤维化
弹性蛋白
机械转化
神经科学
病理
肌成纤维细胞
肺纤维化
纤维细胞
生物信息学
计算生物学
调节器
中断
计算机科学
作者
Patrick A Link,Daniel J. Tschumperlin
标识
DOI:10.1146/annurev-physiol-031725-021041
摘要
Pulmonary fibrosis is a devastating and progressive disease marked by replacement of gas-exchanging tissue with collagen-rich scar. The mechanical environment is profoundly altered in pulmonary fibrosis and contributes to disease progression via feedback relationships between cells, the extracellular matrix, and the evolving mechanical environment. Targeting these mechanobiological feedback loops has emerged as a promising approach to interrupt disease progression, though with challenges in how to intervene selectively, safely, and effectively. We posit that further delineation of cell–matrix mechanobiological interactions will be pivotal to promoting fibrosis resolution and should guide efforts to discover and implement new approaches that can preserve or even restore lung function. To set the stage for these advances, we first review the mechanobiology of the healthy lung and the feedback loops that promote fibrosis progression. We then lay out the challenges and opportunities for targeting the fibrotic matrix as an essential element for protecting or restoring lung function.
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