Tissue-Engineered Lungs for in Vivo Implantation

By T. Petersen, Elizabeth A. Calle, Liping Zhao, E. Lee, Liqiong Gui, MichaSam B. Raredon, Kseniya Gavrilov, T. Yi, Zhuang W. Zhen, C. Breuer and 2 more. Science, 2010

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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. Decellularized rat lungs rebuilt with new cells in vitro can function at a rudimentary level when implanted back into a rat. Because adult lung tissue has limited regeneration capacity, lung transplantation is the primary therapy for severely damaged lungs. To explore whether lung tissue can be regenerated in vitro, we treated lungs from adult rats using a procedure that removes cellular components but leaves behind a scaffold of extracellular matrix that retains the hierarchical branching structures of airways and vasculature. We then used a bioreactor to culture pulmonary epithelium and vascular endothelium on the acellular lung matrix. The seeded epithelium displayed remarkable hierarchical organization within the matrix, and the seeded endothelial cells efficiently repopulated the vascular compartment. In vitro, the mechanical characteristics of the engineered lungs were similar to those of native lung tissue, and when implanted into rats in vivo for short time intervals (45 to 120 minutes) the engineered lungs participated in gas exchange. Although representing only an initial step toward the ultimate goal of generating fully functional lungs in vitro, these results suggest that repopulation of lung matrix is a viable strategy for lung regeneration.

Subfields: Biomaterials, Genetics, Surgery

View Paper: https://www.semanticscholar.org/paper/d5011b815910af4c9321f722d4d4d86810df9e17

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In Biomaterials

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Citations in the corpus

• Acellular normal and fibrotic human lung matrices as a culture system for in vitro investigation. (2012, background): “Grossly, acellular lung maintains a 3Dmorphology similar in appearance to normal lungs (Figure 4), comparable to results achieved in the rodent (13).”
• An overview of tissue and whole organ decellularization processes (2011, background): “The potential advantage of tissue specificity formaintaining selectedcell functionsandphenotypehasbeensuggestedbystudiesof cells and ECM isolated from tissues and organs such as the liver [9,48], respiratory tract [10,30], nerve [49], adipose [50], andmammarygland [51].”