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肺工程程序。

Procedure for lung engineering.

作者信息

Calle Elizabeth A, Petersen Thomas H, Niklason Laura E

机构信息

Department of Biomedical Engineering, Yale University, USA.

出版信息

J Vis Exp. 2011 Mar 8(49):2651. doi: 10.3791/2651.

Abstract

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. 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.

摘要

肺组织,包括肺癌以及慢性阻塞性肺疾病等慢性肺部疾病,每年累计导致约28万人死亡;慢性阻塞性肺疾病目前是美国第四大死因。肺部通常无法在微观细胞水平以上进行修复或再生,这导致了这种高死亡率。因此,因退化或感染而受损的肺组织,或经手术切除的肺组织,在体内无法被功能性替代。为了探究是否能够在体外生成肺组织,我们采用一种去除细胞成分的方法处理成年大鼠的肺,以产生无细胞肺细胞外基质支架。该支架保留了气道和脉管系统的分级分支结构,以及基本完整的基底膜,基底膜由IV型胶原蛋白、层粘连蛋白和纤连蛋白组成。该支架安装在一个生物反应器中,该生物反应器旨在模拟肺生理学的关键方面,如负压通气和搏动性血管灌注。通过在安装于生物反应器的支架内培养肺上皮细胞和血管内皮细胞,我们能够生成在表型上与天然肺组织相当的肺组织,并且能够在短时间间隔(45 - 120分钟)内参与气体交换。这些结果令人鼓舞,并表明肺基质的再细胞化是肺再生的一种可行策略。这种可能性不仅为增加用于移植的肺组织供应提供了机会,还为在比以往更准确的微环境中、更长时间地体外研究呼吸细胞和分子生物学提供了机会。

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