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缺氧在提高间充质基质细胞治疗潜力中的作用。一项针对婴儿健康肺组织和先天性肺气道畸形的比较研究。

The Role of Hypoxia in Improving the Therapeutic Potential of Mesenchymal Stromal Cells. A Comparative Study From Healthy Lung and Congenital Pulmonary Airway Malformations in Infants.

作者信息

Silvestro Serena, Diomede Francesca, Chiricosta Luigi, Zingale Valeria Domenica, Marconi Guya Diletta, Pizzicannella Jacopo, Valeri Andrea, Avanzini Maria Antonietta, Calcaterra Valeria, Pelizzo Gloria, Mazzon Emanuela

机构信息

IRCCS Centro Neurolesi "Bonino-Pulejo", Messina, Italy.

Department of Innovative Technologies in Medicine and Dentistry, University "G. D'Annunzio" Chieti-Pescara, Chieti, Italy.

出版信息

Front Bioeng Biotechnol. 2022 Jun 14;10:868486. doi: 10.3389/fbioe.2022.868486. eCollection 2022.

Abstract

Mesenchymal stromal cells (MSCs) play an important role in the field of regenerative medicine thanks to their immunomodulatory properties and their ability to secrete paracrine factors. The use of MSCs has also been tested in children with congenital lung diseases inducing fibrosis and a decrease in lung function. Congenital malformations of the pulmonary airways (CPAM) are the most frequently encountered lung lesion that results from defects in early development of airways. Despite the beneficial properties of MSCs, interventions aimed at improving the outcome of cell therapy are needed. Hypoxia may be an approach aimed to ameliorate the therapeutic potential of MSCs. In this regard, we evaluated the transcriptomic profile of MSCs collected from pediatric patients with CPAM, analyzing similarities and differences between healthy tissue (MSCs-lung) and cystic tissue (MSCs-CPAM) both in normoxia and in cells preconditioned with hypoxia (0.2%) for 24 h. Study results showed that hypoxia induces cell cycle activation, increasing in such a way the cell proliferation ability, and enhancing cell anaerobic metabolism in both MSCs-lung and MSCs-CPAM-lung. Additionally, hypoxia downregulated several pro-apoptotic genes preserving MSCs from apoptosis and, at the same time, improving their viability in both comparisons. Finally, data obtained indicates that hypoxia leads to a greater expression of genes involved in the regulation of the cytoskeleton in MSCs-lung than MSCs-CPAM.

摘要

间充质基质细胞(MSCs)因其免疫调节特性和分泌旁分泌因子的能力,在再生医学领域发挥着重要作用。MSCs的应用也已在患有导致肺纤维化和肺功能下降的先天性肺部疾病的儿童中进行了测试。先天性肺气道畸形(CPAM)是最常见的肺部病变,由气道早期发育缺陷引起。尽管MSCs具有有益特性,但仍需要旨在改善细胞治疗效果的干预措施。缺氧可能是一种旨在改善MSCs治疗潜力的方法。在这方面,我们评估了从患有CPAM的儿科患者收集的MSCs的转录组概况,分析了常氧和经缺氧(0.2%)预处理24小时的细胞中健康组织(MSCs-肺)和囊性组织(MSCs-CPAM)之间的异同。研究结果表明,缺氧诱导细胞周期激活,从而提高细胞增殖能力,并增强MSCs-肺和MSCs-CPAM-肺中的细胞无氧代谢。此外,缺氧下调了几个促凋亡基因,使MSCs免于凋亡,同时在两种比较中提高了它们的活力。最后,获得的数据表明,与MSCs-CPAM相比,缺氧导致MSCs-肺中参与细胞骨架调节的基因表达更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f51/9237219/6fa31564358e/fbioe-10-868486-g001.jpg

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