Department of Biomedical Engineering, Duke University, Durham, NC, USA.
Cell Transplant. 2011;20(7):1117-26. doi: 10.3727/096368910X544933. Epub 2010 Nov 19.
In this article we describe the design and validation of a bioreactor for the in vitro culture of whole rodent lung tissue. Many current systems only enable large segments of lung tissue to be studied ex vivo for up to a few hours in the laboratory. This limitation restricts the study of pulmonary biology in controlled laboratory settings, and also impacts the ability to reliably culture engineered lung tissues in the laboratory. Therefore, we designed, built, and validated a bioreactor intended to provide sufficient nutrient supply and mechanical stimulation to support cell survival and differentiation in cultured lung tissue. We also studied the effects of perfusion and ventilation on pulmonary cell survival and maintenance of cell differentiation state. The final bioreactor design described herein is capable of supporting the culture of whole native lung tissue for up to 1 week in the laboratory, and offers promise in the study of pulmonary biology and the development of engineered lung tissues in the laboratory.
在本文中,我们描述了一种用于体外培养完整啮齿动物肺组织的生物反应器的设计和验证。许多当前的系统仅允许对实验室中长达几个小时的大段肺组织进行离体研究。这种限制限制了在受控实验室环境中对肺生物学的研究,也影响了在实验室中可靠培养工程化肺组织的能力。因此,我们设计、构建和验证了一种生物反应器,旨在为培养的肺组织提供足够的营养供应和机械刺激,以支持细胞存活和分化。我们还研究了灌流和通气对肺细胞存活和维持细胞分化状态的影响。本文中描述的最终生物反应器设计能够在实验室中支持整个天然肺组织长达 1 周的培养,并有望在肺生物学研究和工程化肺组织的实验室开发中发挥作用。