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Uses of Remnant Human Lung Tissue for Mechanical Stretch Studies

机译:用于机械拉伸研究的残余人肺组织的用途

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摘要

Human lung tissue donated for research purposes is a precious resource which can enhance the exploration of mechanisms involved in ventilator-induced lung injury (VILI). The goal of this work was to establish methods and demonstrate the feasibility of obtaining viable primary human type I-like alveolar epithelial cells (AECs) from remnant tissue, even after a significant lapse in post-mortem time, as well as human precision-cut lung slices (PCLSs), and stretch them at magnitudes correlated with mechanical ventilation volumes. Although after 3 days in culture many of the isolated cells stained for the type II AEC marker pro-surfactant Protein C (pro-SPC), after 6 days in culture the monolayer stained only weakly and non-specifically for pro-SPC, and stained brightly for the type I AEC marker aquaporin-5. A strong zona-occludin 1 stain demonstrated the formation of tight junctions between the cells in the epithelial monolayer after only 3 days in culture. To demonstrate the utility of the preparations for the study of lung injury, we stretched the cells and the PCLSs cyclically, uniformly, and equibiaxially and quantified their viability. Our data show that the described methods allow the utilization of human tissue in in vitro stretch studies investigating VILI.
机译:为研究目的捐赠的人肺组织是一种宝贵的资源,可以增强对呼吸机诱发的肺损伤(VILI)涉及的机制的探索。这项工作的目的是建立方法,并证明从尸体残留组织中获得存活的人类I型样肺泡上皮细胞(AEC)的可行性,甚至在死后时间以及人类精确切割后也是如此肺片(PCLSs),并以与机械通气量相关的幅度拉伸它们。尽管培养3天后,许多分离的细胞对II型AEC标志物前表面活性剂蛋白C(pro-SPC)进行了染色,但是在培养6天后,单层细胞仅对pro-SPC进行了弱且非特异性的染色,并进行了染色对于I型AEC标记aquaporin-5而言,该方法非常有用。仅在培养3天后,强烈的透明带蛋白1染色证明上皮单层细胞之间紧密连接的形成。为了证明该制剂可用于研究肺损伤,我们周期性地,均匀地,等双轴地拉伸细胞和PCLS,并定量了它们的生存能力。我们的数据表明,所描述的方法允许在研究VILI的体外拉伸研究中利用人体组织。

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