Inhalation of lung spheroid cell secretome and exosomes promotes lung repair in pulmonary fibrosis

Phuong‐Uyen Dinh(North Carolina State University), Dipti Paudel(North Carolina State University), Hayden Brochu(North Carolina State University), Kristen D. Popowski(North Carolina State University), M. Cyndell Gracieux(North Carolina State University), Jhon Cores(University of North Carolina at Chapel Hill), Ke Huang(North Carolina State University), Michael Taylor Hensley(North Carolina State University), Erin Harrell(North Carolina State University), Adam C. Vandergriff(University of North Carolina at Chapel Hill), Arianna George(North Carolina State University), Raina T. Barrio(North Carolina State University), Shiqi Hu(University of North Carolina at Chapel Hill), Tyler A. Allen(North Carolina State University), Kevin Blackburn(North Carolina State University), Thomas G. Caranasos(University of North Carolina at Chapel Hill), Xinxia Peng(North Carolina State University), Lauren V. Schnabel(North Carolina State University), Kenneth B. Adler(North Carolina State University), Leonard J. Lobo(University of North Carolina at Chapel Hill), Michael B. Goshe(North Carolina State University), Ke Cheng(University of North Carolina at Chapel Hill)
Nature Communications
February 28, 2020
Cited by 433Open Access
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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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