Tissue-Engineered Lungs for in Vivo Implantation

Author:

Petersen Thomas H.12,Calle Elizabeth A.1,Zhao Liping3,Lee Eun Jung3,Gui Liqiong3,Raredon MichaSam B.1,Gavrilov Kseniya4,Yi Tai5,Zhuang Zhen W.6,Breuer Christopher5,Herzog Erica6,Niklason Laura E.13

Affiliation:

1. Department of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.

2. Department of Biomedical Engineering, Duke University, Durham, NC 27708, USA.

3. Department of Anesthesia, Yale University, New Haven, CT 06520, USA.

4. Department of Cellular and Molecular Physiology, Yale University, New Haven, CT 06520, USA.

5. Department of Surgery, Yale University, New Haven, CT 06520, USA.

6. Department of Internal Medicine, Yale University, New Haven, CT 06520, USA.

Abstract

Waiting to Exhale Lung tissue does not regenerate, so, when it is damaged by disease and/or surgically removed, lung transplantation is often the only treatment option. Because donor tissue is in short supply, there has been a long-standing interest in engineering functional and transplantable lung tissue in the laboratory. Petersen et al. (p. 538 , published online 24 June; see the Perspective by Wagner and Griffith ) now report an important step in this direction. After gently removing the cellular constituents of rat lungs with detergent, the residual scaffold of extracellular matrix—which retained the compliance and mechanical properties of the original lung—was re-seeded with a mixture of lung epithelial and endothelial cells and cultured in a bioreactor. Within a few days, the engineered lung tissue contained alveoli, microvessels, and small airways that were repopulated with the appropriate cell types. When transplanted into a rat for short time periods, the engineered lung showed evidence of gas exchange.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference23 articles.

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5. Whole organ decellularization - a tool for bioscaffold fabrication and organ bioengineering

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