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三维培养的人脐带间充质干细胞通过改善线粒体融合和裂变的平衡来减轻肺纤维化。

Three-dimensional cultured human umbilical cord mesenchymal stem cells attenuate pulmonary fibrosis by improving the balance of mitochondrial fusion and fission.

机构信息

Department of Clinical Nursing, Binzhou Medical University Hospital, Binzhou Medical University, Binzhou 256603, People's Republic of China.

Department of Cellular and Genetic Medicine, Binzhou Medical University, Yantai 264003, People's Republic of China.

出版信息

Stem Cells Transl Med. 2024 Sep 10;13(9):912-926. doi: 10.1093/stcltm/szae051.

DOI:10.1093/stcltm/szae051
PMID:39077914
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11386227/
Abstract

Pulmonary fibrosis is a kind of fibrotic interstitial pneumonia with poor prognosis. Aging, environmental pollution, and coronavirus disease 2019 are considered as independent risk factors for pulmonary fibrogenesis. Consequently, the morbidity and mortality striking continues to rise in recent years. However, the clinical therapeutic efficacy is very limited and unsatisfactory. So it is necessary to develop a new effective therapeutic approach for pulmonary fibrosis. Human umbilical cord mesenchymal stem cells (hucMSCs) are considered as a promising treatment for various diseases because of their multiple differentiation and immunomodulatory function. The key bottleneck in the clinical application of hucMSCs therapy is the high-quality and large-scale production. This study used FloTrix miniSpin bioreactor, a three-dimensional (3D) cell culture system, for large-scale expansion of hucMSCs in vitro, and proved 3D cultured hucMSCs inhibited the differentiation of fibroblasts into myofibroblasts and myofibroblasts proliferation and migration, leading to slow down the development of pulmonary fibrosis. Further mechanistic studies clarified that hucMSCs reduced the amount of binding between circELP2 and miR-630, resulting in blocking YAP/TAZ translocation from cytoplasm to nucleus. This condition inhibited mitochondrial fusion and promoted mitochondrial fission, and ultimately improved fusion/fission balance and cellular homeostasis. To sum up, this work clarified the anti-fibrosis and mechanism of hucMSCs cultured from the 3D FloTrix miniSpin bioreactor. We hope to provide new ideas and new methods for the clinical transformation and industrialization of hucMSCs therapy.

摘要

肺纤维化是一种预后不良的纤维性间质性肺炎。衰老、环境污染和 2019 年冠状病毒病被认为是肺纤维化发生的独立危险因素。因此,近年来发病率和死亡率持续上升。然而,临床治疗效果非常有限,不尽如人意。因此,有必要开发一种新的有效的肺纤维化治疗方法。人脐带间充质干细胞(hucMSCs)因其多向分化和免疫调节功能而被认为是治疗各种疾病的一种有前途的方法。hucMSCs 治疗的临床应用的关键瓶颈是高质量和大规模的生产。本研究使用 FloTrix miniSpin 生物反应器,一种三维(3D)细胞培养系统,体外大规模扩增 hucMSCs,并证明 3D 培养的 hucMSCs 抑制成纤维细胞向肌成纤维细胞分化以及肌成纤维细胞增殖和迁移,从而减缓肺纤维化的发展。进一步的机制研究表明,hucMSCs 减少了 circELP2 与 miR-630 之间的结合量,从而阻止了 YAP/TAZ 从细胞质向细胞核的易位。这种情况抑制了线粒体融合并促进了线粒体裂变,最终改善了融合/裂变平衡和细胞内稳态。总之,这项工作从 3D FloTrix miniSpin 生物反应器培养的 hucMSCs 阐明了抗纤维化和机制。我们希望为 hucMSCs 治疗的临床转化和产业化提供新的思路和新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/8e07c80167d6/szae051_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/933c05236293/szae051_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/7a74cd191770/szae051_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/4b7ac5649112/szae051_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/ad66677be1c8/szae051_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/c9d9f2f8972a/szae051_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/29ccb7d9ac69/szae051_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/8e07c80167d6/szae051_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/933c05236293/szae051_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/7a74cd191770/szae051_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/4b7ac5649112/szae051_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/ad66677be1c8/szae051_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/c9d9f2f8972a/szae051_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/29ccb7d9ac69/szae051_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d55/11386227/8e07c80167d6/szae051_fig6.jpg

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Cell Death Dis. 2023 Sep 2;14(9):585. doi: 10.1038/s41419-023-06112-4.
2
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Nat Rev Mol Cell Biol. 2023 Dec;24(12):895-911. doi: 10.1038/s41580-023-00644-5. Epub 2023 Aug 25.
3
OPA1, a molecular regulator of dilated cardiomyopathy.OPA1,扩张型心肌病的分子调节因子。
J Cell Mol Med. 2023 Oct;27(20):3017-3025. doi: 10.1111/jcmm.17918. Epub 2023 Aug 21.
4
Endoplasmic reticulum stress induced by turbulence of mitochondrial fusion and fission was involved in stressed cardiomyocyte injury.线粒体融合和裂变的湍流引起的内质网应激参与了应激性心肌细胞损伤。
J Cell Mol Med. 2023 Nov;27(21):3313-3325. doi: 10.1111/jcmm.17901. Epub 2023 Aug 18.
5
Molecular mechanisms and treatment responses of pulmonary fibrosis in severe COVID-19.严重 COVID-19 中肺纤维化的分子机制和治疗反应。
Respir Res. 2023 Aug 9;24(1):196. doi: 10.1186/s12931-023-02496-1.
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