Abstract

Acute exposure to high-dose gamma radiation due to radiological disasters or cancer radiotherapy can result in radiation-induced lung injury (RILI), characterized by acute pneumonitis and subsequent lung fibrosis. A microfluidic organ-on-a-chip lined by human lung alveolar epithelium interfaced with pulmonary endothelium (Lung Alveolus Chip) is used to model acute RILI in vitro. Both lung epithelium and endothelium exhibit DNA damage, cellular hypertrophy, upregulation of inflammatory cytokines, and loss of barrier function within 6 h of radiation exposure, although greater damage is observed in the endothelium. The radiation dose sensitivity observed on-chip is more like the human lung than animal preclinical models. The Alveolus Chip is also used to evaluate the potential ability of two drugs - lovastatin and prednisolone - to suppress the effects of acute RILI. These data demonstrate that the Lung Alveolus Chip provides a human relevant alternative for studying the molecular basis of acute RILI and may be useful for evaluation of new radiation countermeasure therapeutics.

Acute exposure to radiation can lead to acute pneumonitis, fibrosis or death. Here the authors develop an alveolus-on chip model to study the molecular characteristics of radiation induced lung injury, better understand radiation induced lung disease and facilitate drug screening.

Details

Title
A human lung alveolus-on-a-chip model of acute radiation-induced lung injury
Author
Dasgupta, Queeny 1 ; Jiang, Amanda 1 ; Wen, Amy M. 2 ; Mannix, Robert J. 3 ; Man, Yuncheng 1   VIAFID ORCID Logo  ; Hall, Sean 2 ; Javorsky, Emilia 2 ; Ingber, Donald E. 4   VIAFID ORCID Logo 

 Boston Children’s Hospital and Harvard Medical School, Vascular Biology Program and Department of Surgery, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, USA (GRID:grid.38142.3c) 
 Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, USA (GRID:grid.38142.3c) 
 Boston Children’s Hospital and Harvard Medical School, Vascular Biology Program and Department of Surgery, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X) 
 Boston Children’s Hospital and Harvard Medical School, Vascular Biology Program and Department of Surgery, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Wyss Institute for Biologically Inspired Engineering at Harvard University, Boston, USA (GRID:grid.38142.3c); Harvard University, Harvard John A. Paulson School of Engineering and Applied Sciences, Cambridge, USA (GRID:grid.38142.3c) (ISNI:0000 0004 1936 754X) 
Pages
6506
Publication year
2023
Publication date
2023
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2877591979
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.