特发性肺纤维化
博莱霉素
肺
肺纤维化
纤维化
肌成纤维细胞
医学
病理
吸入
外体
微泡
间充质干细胞
癌症研究
化学
内科学
解剖
化疗
小RNA
基因
生物化学
作者
Phuong‐Uyen Dinh,Dipti Paudel,Hayden Brochu,Kristen D. Popowski,M. Cyndell Gracieux,Jhon Cores,Ke Huang,Michael Taylor Hensley,Erin Harrell,Adam C. Vandergriff,Arianna George,Raina T. Barrio,Shiqi Hu,Tyler A. Allen,Kevin Blackburn,Thomas G. Caranasos,Xinxia Peng,Lauren V. Schnabel,Kenneth B. Adler,Leonard J. Lobo,Michael B. Goshe,Ke Cheng
标识
DOI:10.1038/s41467-020-14344-7
摘要
Abstract Idiopathic pulmonary fibrosis (IPF) is a fatal and incurable form of interstitial lung disease in which persistent injury results in scar tissue formation. As fibrosis thickens, the lung tissue loses the ability to facilitate gas exchange and provide cells with needed oxygen. Currently, IPF has few treatment options and no effective therapies, aside from lung transplant. Here we present a series of studies utilizing lung spheroid cell-secretome (LSC-Sec) and exosomes (LSC-Exo) by inhalation to treat different models of lung injury and fibrosis. Analysis reveals that LSC-Sec and LSC-Exo treatments could attenuate and resolve bleomycin- and silica-induced fibrosis by reestablishing normal alveolar structure and decreasing both collagen accumulation and myofibroblast proliferation. Additionally, LSC-Sec and LSC-Exo exhibit superior therapeutic benefits than their counterparts derived from mesenchymal stem cells in some measures. We showed that an inhalation treatment of secretome and exosome exhibited therapeutic potential for lung regeneration in two experimental models of pulmonary fibrosis.
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