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人脐带间充质干细胞来源的外泌体通过抑制铁死亡减轻烧伤诱导的急性肺损伤。

Human umbilical cord mesenchymal stem cells-derived exosomes attenuate burn-induced acute lung injury via inhibiting ferroptosis.

机构信息

Department of Burn and Plastic Surgery, The Third People's Hospital of Bengbu Affiliated to Bengbu Medical University, Bengbu 233000, China.

Department of Burn and Plastic Surgery, Affiliated Hospital of Jiangnan University, Wuxi 214028, China.

出版信息

Acta Histochem. 2024 Oct;126(5-7):152189. doi: 10.1016/j.acthis.2024.152189. Epub 2024 Aug 27.

Abstract

Our previous study has shown that exosomes derived from human umbilical cord mesenchymal stem cells (hUCMSCs-exo) alleviated burn-induced acute lung injury (ALI). In this study, we explored a novel mechanism by which hUCMSCs-exo contributed to the inhibition of burn-induced ALI. The ALI rat model with severe burn was established for the in vivo experiments, and rats PMVECs were stimulated with the serum from burn-induced ALI rats for the in vitro experiments. The pathological changes of lung tissues were evaluated by HE staining; the cell viability was measured using CCK-8; the iron level and Fe concentration were assessed using Iron Assay Kit and Fe fluorescence detection probe; the mRNA expression of SLC7A11 and GPX4 were measured by qRT-PCR; the protein levels of SLC7A11, GPX4, Nrf2 and HO-1 were detected by western blot. Both the in vivo and in vitro experiments revealed that ferroptosis was significantly induced in burn-induced ALI, which as verified by increased iron level and Fe concentration, and decreased SLC7A11 and GPX4 mRNA and protein levels. Furthermore, both hUCMSCs-exo and Fer-1 (the inhibitor of ferroptosis) alleviated lung inflammation and up-regulated protein levels of Nrf2 and HO-1 in the lung tissues of burn-induced ALI rats. These results suggested that hUCMSCs-exo exhibited a protective role against burn-induced ALI by inhibiting ferroptosis, partly owing to the activation of Nrf2/HO-1 pathway, thus providing a novel therapeutic strategy for burn-induced ALI.

摘要

我们之前的研究表明,人脐带间充质干细胞来源的外泌体(hUCMSCs-exo)缓解了烧伤诱导的急性肺损伤(ALI)。在本研究中,我们探索了 hUCMSCs-exo 抑制烧伤诱导的 ALI 的新机制。为了进行体内实验,我们建立了严重烧伤的 ALI 大鼠模型,为了进行体外实验,我们用烧伤诱导的 ALI 大鼠的血清刺激大鼠 PMVECs。通过 HE 染色评估肺组织的病理变化;使用 CCK-8 测量细胞活力;使用铁含量测定试剂盒和 Fe 荧光检测探针评估铁水平和 Fe 浓度;通过 qRT-PCR 测量 SLC7A11 和 GPX4 的 mRNA 表达;通过 Western blot 检测 SLC7A11、GPX4、Nrf2 和 HO-1 的蛋白水平。体内和体外实验均表明,烧伤诱导的 ALI 中明显诱导了铁死亡,这通过增加铁水平和 Fe 浓度以及降低 SLC7A11 和 GPX4 的 mRNA 和蛋白水平得到证实。此外,hUCMSCs-exo 和 Fer-1(铁死亡抑制剂)均缓解了烧伤诱导的 ALI 大鼠的肺部炎症,并上调了肺部 Nrf2 和 HO-1 的蛋白水平。这些结果表明,hUCMSCs-exo 通过抑制铁死亡对烧伤诱导的 ALI 发挥保护作用,部分原因是激活了 Nrf2/HO-1 通路,从而为烧伤诱导的 ALI 提供了一种新的治疗策略。

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