Mechanobiology of Lung Fibrosis

肺纤维化的力学生物学

基本信息

批准号：
7729005
负责人：
Daniel J. Tschumperlin
金额：
$ 42.89万
依托单位：
HARVARD SCHOOL OF PUBLIC HEALTH
依托单位国家：
美国
项目类别：
财政年份：
2009
资助国家：
美国
起止时间：
2009-08-06 至 2013-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7729005
关键词：
Actins Affect Apoptosis Atomic Force Microscopy Automobile Driving Behavior Bioinformatics Biological Biology Bleomycin Bronchoalveolar Lavage Fluid Cell Culture Techniques Cells Data Deposition Disease Employee Strikes Environment Exhibits F-Actin Feedback Fibroblasts Fibrosis Focal Adhesions G Actin Gases Gel Gene Expression Gene Proteins Growth Hamman-Rich syndrome Human Immunofluorescence Immunologic Interstitial Lung Diseases Knowledge Lead Lesion Link Lung Measurement Mechanics Modeling Molecular Mus Myofibroblast Outcome Phenotype Play Pulmonary Fibrosis RNA Interference Regulator Genes Research Role Saline Serum Serum Response Factor Signal Transduction Stress Fibers Structure of parenchyma of lung Testing Tissues base cytokine fibrogenesis insight lung injury novel polyacrylamide gels polymerization preconditioning programs protein expression public health relevance research study response therapeutic target three-dimensional modeling transcription factor

项目摘要

DESCRIPTION (provided by applicant): Progressive fibrosis is a hallmark of interstitial lung diseases such as idiopathic pulmonary fibrosis. Fibrosis stiffens the lung parenchyma. Preliminary data provided in this proposal demonstrate that normal lung parenchymal tissue is more compliant than previously predicted, and that highly localized increases in the stiffness of fibrotic lesions are much greater than previously recognized. Fibroblasts grown on substrates as stiff as fibrotic lesions engage in rapid proliferation and abundant matrix synthesis; in marked contrast these behaviors are largely suppressed on substrates as compliant as normal lung tissue. The central hypothesis that we pose based on these data is that the mechanical environment present in lung fibrosis triggers a "fibrogenesis program" in resident fibroblasts that promotes feedback amplification of the disease. We propose four specific aims: (1) quantify the stiffness of the parenchyma in normal lung tissue and developing and established fibrotic lesions; (2) test whether the transition in matrix stiffness from normal to fibrotic levels is a necessary precondition for lung fibroblast proliferation and fibrogenic activation; (3) test the role played by cytoskeletal dynamics and serum response factor activation in driving stiffness-dependent fibroblast biology; and (4) identify key transcription factors coordinating fibroblast transitions between quiescent and fibrogenic states when transferred between compliant and stiff matrices. These aims will be carried out in novel 2D and 3D models that allow clear delineation of the effects of lung matrix stiffness on key fibrogenic behaviors of lung fibroblasts. Throughout the experimental plan we will examine the interplay between matrix stiffness and the soluble environment present in fibrosis as it impacts on fibroblast biology. This research will generate novel insights into the molecular mechanisms of stiffness-dependent fibroblast activation in fibrotic lungs, and identify critical regulators of fibrogenesis suitable for therapeutic targeting. PUBLIC HEALTH RELEVANCE: Lung fibrosis stiffens affected tissue. The experiments proposed here will test whether pathophysiological changes in stiffness promote fibrosis by stimulating lung fibroblasts. Understanding the role mechanical factors play in fibroblast activation could lead to new strategies to treat fibrosis.

描述（由申请人提供）：进行性纤维化是间质性肺疾病（例如特发性肺纤维化）的标志。纤维化使肺实质变硬。该提案中提供的初步数据表明，正常肺实质组织比之前预测的更顺应，并且纤维化病变的硬度的高度局部增加比之前认识到的要大得多。在像纤维化病变一样坚硬的基质上生长的成纤维细胞参与快速增殖和丰富的基质合成；与此形成鲜明对比的是，这些行为在与正常肺组织一样顺应的基质上很大程度上受到抑制。我们基于这些数据提出的中心假设是，肺纤维化中存在的机械环境触发了常驻成纤维细胞中的“纤维发生程序”，从而促进了疾病的反馈放大。我们提出了四个具体目标：（1）量化正常肺组织以及正在形成和形成的纤维化病变中实质的硬度； (2)测试基质硬度从正常水平向纤维化水平的转变是否是肺成纤维细胞增殖和纤维化激活的必要前提； (3)测试细胞骨架动力学和血清反应因子激活在驱动刚度依赖性成纤维细胞生物学中所起的作用； (4)确定在顺应性基质和刚性基质之间转移时协调成纤维细胞在静止状态和成纤维状态之间转变的关键转录因子。这些目标将在新型 2D 和 3D 模型中实现，这些模型可以清楚地描绘肺基质硬度对肺成纤维细胞关键纤维形成行为的影响。在整个实验计划中，我们将检查基质硬度与纤维化中存在的可溶性环境之间的相互作用，因为它对成纤维细胞生物学产生影响。这项研究将对纤维化肺中硬度依赖性成纤维细胞激活的分子机制产生新的见解，并确定适合治疗靶向的纤维发生的关键调节因子。公共卫生相关性：肺纤维化使受影响的组织变硬。这里提出的实验将测试僵硬的病理生理变化是否通过刺激肺成纤维细胞促进纤维化。了解机械因素在成纤维细胞活化中的作用可能会导致治疗纤维化的新策略。