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Three-Dimensionally Engineered Normal Human Lung Tissue-Like Assemblies: Target Tissues for Human Respiratory Viral InfectionsIn vitro three-dimensional (3D) human lung epithelio-mesenchymal tissue-like assemblies (3D hLEM TLAs) from this point forward referred to as TLAs were engineered in Rotating Wall Vessel (RWV) technology to mimic the characteristics of in vivo tissues thus providing a tool to study human respiratory viruses and host cell interactions. The TLAs were bioengineered onto collagen-coated cyclodextran microcarriers using primary human mesenchymal bronchial-tracheal cells (HBTC) as the foundation matrix and an adult human bronchial epithelial immortalized cell line (BEAS-2B) as the overlying component. The resulting TLAs share significant characteristics with in vivo human respiratory epithelium including polarization, tight junctions, desmosomes, and microvilli. The presence of tissue-like differentiation markers including villin, keratins, and specific lung epithelium markers, as well as the production of tissue mucin, further confirm these TLAs differentiated into tissues functionally similar to in vivo tissues. Increasing virus titers for human respiratory syncytial virus (wtRSVA2) and the detection of membrane bound glycoproteins over time confirm productive infection with the virus. Therefore, we assert TLAs mimic aspects of the human respiratory epithelium and provide a unique capability to study the interactions of respiratory viruses and their primary target tissue independent of the host s immune system.
Document ID
20080012580
Acquisition Source
Johnson Space Center
Document Type
Other
Authors
Goodwin, Thomas J.
(NASA Johnson Space Center Houston, TX, United States)
McCarthy, M.
(NASA Johnson Space Center Houston, TX, United States)
Lin, Y-H.
(Wyeth Research New York, United States)
Deatly, A. M.
(Wyeth Research New York, United States)
Date Acquired
August 24, 2013
Publication Date
February 11, 2008
Subject Category
Life Sciences (General)
Funding Number(s)
CONTRACT_GRANT: NAS9-17720
Distribution Limits
Public
Copyright
Public Use Permitted.
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