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诱导多能干细胞分化为肺泡Ⅱ型上皮细胞系。

Generation of an alveolar epithelial type II cell line from induced pluripotent stem cells.

机构信息

Department of Pulmonary Medicine, University Hospital Bern, University of Bern , Bern, Switzerland.

Graduate School for Cellular and Biomedical Sciences, University of Bern , Bern, Switzerland.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2018 Dec 1;315(6):L921-L932. doi: 10.1152/ajplung.00357.2017. Epub 2018 Sep 13.

Abstract

Differentiation of primary alveolar type II epithelial cells (AEC II) to AEC type I in culture is a major barrier in the study of the alveolar epithelium in vitro. The establishment of an AEC II cell line derived from induced pluripotent stem cells (iPSC) represents a novel opportunity to study alveolar epithelial cell biology, for instance, in the context of lung injury, fibrosis, and repair. In the present study, we generated long-lasting AEC II from iPSC (LL-iPSC-AEC II). LL-iPSC-AEC II displayed morphological characteristics of AEC II, including growth in a cobblestone monolayer, the presence of lamellar bodies, and microvilli, as shown by electron microscopy. Also, LL-iPSC-AEC II expressed AEC type II proteins, such as cytokeratin, surfactant protein C, and LysoTracker DND 26 (a marker for lamellar bodies). Furthermore, the LL-iPSC-AEC II exhibited functional properties of AEC II by an increase of transepithelial electrical resistance over time, secretion of inflammatory mediators in biologically relevant quantities (IL-6 and IL-8), and efficient in vitro alveolar epithelial wound repair. Consistent with the AEC II phenotype, the cell line showed the ability to uptake and release surfactant protein B, to secrete phospholipids, and to differentiate into AEC type I. In summary, we established a long-lasting, but finite AEC type II cell line derived from iPSC as a novel cellular model to study alveolar epithelial cell biology in lung health and disease.

摘要

在体外研究肺泡上皮细胞时,将初级肺泡 II 型上皮细胞(AEC II)分化为 AEC I 是一个主要障碍。从诱导多能干细胞(iPSC)中建立 AEC II 细胞系为研究肺泡上皮细胞生物学提供了一个新的机会,例如在肺损伤、纤维化和修复的背景下。在本研究中,我们从 iPSC 中生成了持久的 AEC II(LL-iPSC-AEC II)。LL-iPSC-AEC II 表现出 AEC II 的形态特征,包括在鹅卵石单层中生长、存在板层小体和微绒毛,如电子显微镜所示。此外,LL-iPSC-AEC II 表达 AEC II 型蛋白,如细胞角蛋白、表面活性蛋白 C 和 LysoTracker DND 26(板层小体的标志物)。此外,LL-iPSC-AEC II 通过随时间增加的跨上皮电阻来表现出 AEC II 的功能特性,以生物相关量分泌炎症介质(IL-6 和 IL-8),并有效地进行体外肺泡上皮细胞伤口修复。与 AEC II 表型一致,该细胞系显示出摄取和释放表面活性蛋白 B、分泌磷脂以及分化为 AEC I 的能力。总之,我们建立了一种源自 iPSC 的持久但有限的 AEC II 细胞系,作为研究肺健康和疾病中肺泡上皮细胞生物学的新型细胞模型。

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