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  1. MCM Regulatory Science

Human organ chips for radiation countermeasure development

Scientists are developing models of radiation damage in lung, gut, & bone marrow organs-on-chips and using these models to test MCMs to treat such damage

The Wyss Institute’s gut-on-a-chip constricts and relaxes, just as in the human body, producing finger-like projections called villi, shown at left. (Credit: Wyss Institute at Harvard University)
The Wyss Institute’s gut-on-a-chip constricts and relaxes, just as in the human body, producing finger-like projections called villi, shown at left. (Credit: Wyss Institute at Harvard University)

Leveraging human organ chips with a computational discovery pipeline to replicate clinical responses to radiation exposure and develop new medical countermeasures

Background | Project description | Project outcomes | Publications | Related links

Performer: Wyss Institute for Biologically Inspired Engineering at Harvard University
Principal investigator: Donald E. Ingber, MD, PhD
Contract value: $3,588,882
Project dates: September 2019 – September 2021


Acute radiation syndrome (ARS) is an illness affecting a combination of organs that occurs when the body receives a high dose of radiation over a short period of time, as could occur after a nuclear or radiological incident. The U.S. government has identified a need for safe and effective radiation medical countermeasures (MCMs) for military and civilian applications, as well as to mitigate toxicities associated with medical radiotherapies.

The development of MCMs to treat ARS presents complex scientific challenges. For example, ARS may involve many organ systems, which makes it difficult to study candidate MCMs that target the radiation effects on one specific organ system in animal models. Thus, there is a crucial need for more predictive in vitro models of the effects of ionizing radiation on human tissue and organ function. Closing such knowledge gaps to further MCM development and availability is a key goal of the MCMi Regulatory Science Program.  

Project description

The Ingber Laboratory at the Wyss Institute has developed human organs-on-chips—microfluidic culture devices that replicate human organ-level pathophysiology. This project builds on past FDA-funded work at the Wyss Institute that led to the development of human models of ARS in bone marrow, intestine, and lung organs-on-chips and the application of these tools to the evaluation of ARS MCMs. Under the current project, the Wyss team will advance the use of human organs-on-chips for MCM development by demonstrating biomimicry and defining critical qualification criteria, helping to reduce the reliance on testing in small animals and nonhuman primates (NHPs).  

Project outcomes

Deliverables from this project include:

  • Assessing the effects of MCMs (FDA-approved and in development) on reducing radiation damage in male versus female bone marrow chips to determine differences in radiation response by sex
  • Analyzing the interplay   between human bone marrow organs-on-chips and intestine organs-on-chips that include a complex human gut microbiome in response to radiation exposure
  • Recapitulating radiation-induced pneumonitis and response to existing ARS MCMs in the human lung alveolus chip
  • Using the Wyss computational discovery pipeline with transcriptomics data to support repurposing existing drugs as radiation MCMs

This project was funded through the MCMi Regulatory Science Extramural Research program


  • Human colon-on-a-chip enables continuous in vitro analysis of colon mucus layer accumulation and physiology. Sontheimer-Phelps A, Chou D, Tovaglieri A, Ferrante T, Duckworth T, Fade C, Frismantas V, Sutherland A, Jalili-Firoozinezhad S, Kasendra M, Stas E, Weaver, J, Richmond C, Levy O, Prantil-Baun R, Breault D, Ingber D. Cell Mol Gastroenterol Hepatol. 2019 Nov 25. pii: S2352-345X(19)30163-8. doi: https://doi.org/10.1016/j.jcmgh.2019.11.008
  • Human bone marrow disorders recapitulated in vitro using organ chip technology. Chou D, Frismantas, V, Other Wyss, Other Az, SDS authors, Ewart L, and Ingber DE. bioRxiv 458935;  doi: https://doi.org/10.1101/458935
  • A complex human gut microbiome cultured in an anaerobic intestine-on-a-chip. Jalili-Firoozinezhad S, Gazzaniga FS, Calamari EL, Camacho DM, Fadel CW, Nestor B, Cronce MJ, Tovaglieri A, Levy O, Gregory KE, Breault DT, Cabral JMS, Kasper DL, Novak R, and Ingber DE. Nature Biomed. Engin. 2019; 3:520-531. doi: https://doi.org/10.1038/s41551-019-0397-0
  • Development of primary human small intestine-on-a-chip using patient-derived organoids. Kasendra M, Tovaglieri A, Sontheimer-Phelps A, Jalili-Firoozinezhad S, Bein A, Chalkiadaki A, Scholl W, Zheng C, Rickner H, Dinis ALM, Richmond CA, Li H, Cartwright M, Super M, Breault DR and Ingber DE. Sci. Rep. 2018; 8:2871  doi: https://doi.org/10.1038/s41598-018-21201-7 
  • Primary human lung alveolus on a chip model of intravascular thrombosis for assessment of therapeutics.  Jain A, Barrile, R, van der Meer A, Mammoto A, Mammoto T, DeCeunyck K, Aisku O, Otieno MA, Louden CS, Hamilton G, Flaumenhaft R, Ingber DE. Clin. Pharmacol. Ther. 2018 Feb;103(2):332-340. doi: https://doi.org/10.1002/cpt.742
  • Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip. Jalili-Firoozinezhad S, Prantil-Baun R, Jiang A, Potla R, Mammoto T, Weaver JC, Ferrante TC, Kim HJ, Cabral JMS, Levy O, Ingber DE. Cell Death Dis. 2018;9(2):223. doi: https://doi.org/10.1038/s41419-018-0304-8
  • Modeling Hematopoiesis and Responses to Radiation Countermeasures in a Bone Marrow-on-a-Chip. Torisawa YS, Mammoto T, Jiang E, Jiang A, Mammoto A, Watters AL, Bahinski A, Ingber DE. Tissue Eng Part C Methods. 2016;22(5):509-15. doi: https://doi.org/10.1089/ten.TEC.2015.0507
  • Bone marrow-on-a-chip replicates hematopoietic niche physiology in vitro. Torisawa YS, Spina CS, Mammoto T, Mammoto A, Weaver JC, Tat T, Collins JJ, Ingber DE. Nat Methods. 2014;11(6):663-9. doi: https://doi.org/10.1038/nmeth.2938 
  • Quantitative prediction of human pharmacokinetic responses to drugs via fluidically coupled vascularized organ chips. Herland A, Maoz BM, Das D, Somayaji MR, Prantil-Baun R, Novak R, Cronce M, Huffstater T, Jeanty SSF, Ingram M, Chalkiadaki A, Benson Chou D, Marquez S, Delahanty A, Jalili-Firoozinezhad S, Milton Y, Sontheimer-Phelps A, Swenor B, Levy O, Parker KK, Przekwas A, Ingber DE. Nat Biomed Eng. 2020 Jan 27. doi: 10.1038/s41551-019-0498-9.

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