Procedure for Lung Engineering

被引:30
作者
Calle, Elizabeth A. [1 ]
Petersen, Thomas H. [2 ]
Niklason, Laura E. [1 ,3 ]
机构
[1] Yale Univ, Dept Biomed Engn, New Haven, CT 06520 USA
[2] Duke Univ, Dept Biomed Engn, Sch Med, Durham, NC 27706 USA
[3] Yale Univ, Dept Anesthesia, New Haven, CT 06520 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2011年 / 49期
关键词
Bioengineering; Issue; 49; Decellularization; tissue engineering; lung engineering; lung tissue; extracellular matrix; II EPITHELIAL-CELLS; IN-VIVO; MATRIX; DIFFERENTIATION;
D O I
10.3791/2651
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lung tissue, including lung cancer and chronic lung diseases such as chronic obstructive pulmonary disease, cumulatively account for some 280,000 deaths annually; chronic obstructive pulmonary disease is currently the fourth leading cause of death in the United States(1). Contributing to this mortality is the fact that lungs do not generally repair or regenerate beyond the microscopic, cellular level. Therefore, lung tissue that is damaged by degeneration or infection, or lung tissue that is surgically resected is not functionally replaced in vivo. To explore whether lung tissue can be generated in vitro, we treated lungs from adult rats using a procedure that removes cellular components to produce an acellular lung extracellular matrix scaffold. This scaffold retains the hierarchical branching structures of airways and vasculature, as well as a largely intact basement membrane, which comprises collagen IV, laminin, and fibronectin. The scaffold is mounted in a bioreactor designed to mimic critical aspects of lung physiology, such as negative pressure ventilation and pulsatile vascular perfusion. By culturing pulmonary epithelium and vascular endothelium within the bioreactor-mounted scaffold, we are able to generate lung tissue that is phenotypically comparable to native lung tissue and that is able to participate in gas exchange for short time intervals (45-120 minutes). These results are encouraging, and suggest that repopulation of lung matrix is a viable strategy for lung regeneration. This possibility presents an opportunity not only to work toward increasing the supply of lung tissue for transplantation, but also to study respiratory cell and molecular biology in vitro for longer time periods and in a more accurate microenvironment than has previously been possible.
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页数:7
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