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人脐带华通氏胶间充质基质细胞逆转了实验性窒息新生模型中的细胞凋亡,预防了多器官损伤。

Human wharton-jelly mesenchymal stromal cells reversed apoptosis and prevented multi-organ damage in a newborn model of experimental asphyxia.

机构信息

Department of Molecular Biotechnology, Graduate School of Health Sciences, Aydin Adnan Menderes University, Aydin, Turkey.

Department of Histology and Embryology, School of Medicine, Aydin Adnan Menderes University, Aydin, Turkey.

出版信息

J Obstet Gynaecol. 2022 Nov;42(8):3568-3576. doi: 10.1080/01443615.2022.2158318. Epub 2023 Jan 13.

DOI:10.1080/01443615.2022.2158318
PMID:36638075
Abstract

In this study, the effect of applying wharton jelly mesenchymal stromal cells (WJ-MSC) isolated from the human umbilical cord tissue on the neonatal mouse model caused experimental asphyxia in mice was investigated. WJ-MSC surface markers (CD44, CD90, CD105) were characterised by immunofluorescence staining, and pluripotency genes (Nanog, Oct-4, Sox-2) were characterised by qPCR. Blood, prefrontal cortex, cerebellum, hippocampus, lung, heart, kidney, and liver tissues were analysed twenty days after subcutaneously administered WJ-MSC. WJ-MSC administration significantly decreased serum TNF-α, NSE, GFAP, and IL-6 levels in the asphyxia mice. It was determined that WJ-MSC application in tissues accelerated cell regeneration and decreased oxidative stress. In conclusion, this study showed that multiorgan damage in asphyxia could be prevented by applying WJ-MSC at an early stage. Therefore, WJ-MSC application in infants with neonatal asphyxia in the clinic may be an innovative method in the future.

摘要

本研究探讨了从人脐带组织中分离的牙髓间充质基质细胞(WJ-MSC)对实验性窒息新生小鼠模型的影响。通过免疫荧光染色对 WJ-MSC 表面标志物(CD44、CD90、CD105)进行了特征描述,并通过 qPCR 对多能基因(Nanog、Oct-4、Sox-2)进行了特征描述。在皮下给予 WJ-MSC 二十天后,分析了血液、前额叶皮层、小脑、海马、肺、心脏、肾脏和肝脏组织。WJ-MSC 给药可显著降低窒息小鼠血清 TNF-α、NSE、GFAP 和 IL-6 水平。结果表明,WJ-MSC 在组织中的应用加速了细胞再生,降低了氧化应激。总之,本研究表明,早期应用 WJ-MSC 可预防窒息引起的多器官损伤。因此,在临床上对新生儿窒息的婴儿应用 WJ-MSC 可能是未来的一种创新方法。

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