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囊性纤维化细胞模型的比较荟萃分析提示存在部分内皮-间充质转化。

Comparative meta-analysis of cystic fibrosis cell models suggests partial endothelial-to-mesenchymal transition.

作者信息

Treps Lucas, Declercq Mathias, Bousfia Siham, Carmeliet Peter, Witters Peter

机构信息

Laboratory of Angiogenesis and Vascular Metabolism, Centre for Cancer Biology, VIB, Leuven, Belgium; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium; Université de Nantes, CNRS, INSERM, CRCINA, F-44000 Nantes, France.

Laboratory of Angiogenesis and Vascular Metabolism, Centre for Cancer Biology, VIB, Leuven, Belgium; Laboratory of Angiogenesis and Vascular Metabolism, Department of Oncology and Leuven Cancer Institute (LKI), KU Leuven, Leuven, Belgium; Department of Development and Regeneration, CF Centre, Woman and Child, KU Leuven, Leuven, Belgium.

出版信息

J Cyst Fibros. 2021 Sep;20(5):876-880. doi: 10.1016/j.jcf.2021.03.019. Epub 2021 Apr 13.

Abstract

The mesenchymal conversion of epithelial cells (EMT) has been suggested as a potential contributor in cystic fibrosis (CF) disease progression. Endothelial cells (EndCs), the cells lining blood vessels, express functional CFTR and CFTR impairment promotes endothelial activation and dysfunction. However, if the mesenchymal switch also exists in CF EndCs remains uncharacterized. To understand whether the endothelial-to-mesenchymal transition (EndMT) could occur in CF, we have conducted a transcriptomic meta-analysis of primary CFTR-impaired and patient-derived EndCs, and further compared our results to data from CF epithelial cells (EpCs) where EMT has been demonstrated. As compared to EpCs, we show that CFTR-impaired EndCs display a limited signature of EndMT, and that expression of the mesenchymal inducer Twist1 remained unchanged. Nonetheless, the use of CFTR modulators reduced the expression of mesenchymal markers from CF patient-derived EndCs, suggesting an additional therapeutic added-value next to the known effect on CFTR ion transport.

摘要

上皮细胞间充质转化(EMT)被认为是囊性纤维化(CF)疾病进展的一个潜在因素。内皮细胞(EndCs),即血管内壁的细胞,表达功能性囊性纤维化跨膜传导调节因子(CFTR),CFTR功能受损会促进内皮细胞激活和功能障碍。然而,CF内皮细胞中是否也存在间充质转变仍不清楚。为了了解CF中是否会发生内皮-间充质转化(EndMT),我们对原发性CFTR功能受损和患者来源的内皮细胞进行了转录组元分析,并将我们的结果与已证实发生EMT的CF上皮细胞(EpCs)的数据进行了进一步比较。与EpCs相比,我们发现CFTR功能受损的EndCs显示出有限的EndMT特征,间充质诱导因子Twist1的表达保持不变。尽管如此,使用CFTR调节剂可降低CF患者来源的EndCs中间充质标志物的表达,这表明除了对CFTR离子转运的已知作用外,还有额外的治疗附加值。

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