Human Umbilical Cord Mesenchymal Stromal Cell-Derived Exosomes Alleviate Hypoxia-Induced Pulmonary Arterial Hypertension in Mice Via Macrophages.

IF 4 2区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
STEM CELLS Pub Date : 2024-04-15 DOI:10.1093/stmcls/sxad098
Hong Liu, Qingqing Zhang, Chuanchuan Liu, Yuwei Zhang, Yuxiang Wang, Pan Huang, Lan Ma, Rili Ge
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引用次数: 0

Abstract

Pulmonary hypertension (PH) is an intractable, severe, and progressive cardiopulmonary disease. Recent findings suggest that human umbilical cord mesenchymal stromal cells (HUCMSCs) and HUCMSC-derived exosomes (HUCMSC-Exos) possess potential therapeutic value for PH. However, whether they have beneficial effects on hypoxic pulmonary hypertension (HPH) is unclear. Exos are released into the extracellular environment by the fusion of intracellular multivesicular bodies with the cell membrane, and they play an important role in cellular communication. Exos ameliorate immune inflammation levels, alter macrophage phenotypes, regulate mitochondrial metabolic function, and inhibit pulmonary vascular remodeling, thereby improving PH. Macrophages are important sources of cytokines and other transmitters and can promote the release of cytokines, vasoactive molecules, and reactive oxygen species, all of which are associated with pulmonary vascular remodeling. Therefore, the aim of this study was to investigate whether HUCMSC-Exos could improve the lung inflammatory microenvironment and inhibit pulmonary vascular remodeling by targeting macrophages and identifying the underlying mechanisms. The results showed that HUCMSC-Exos promoted M2 macrophage polarization, decreased pro-inflammatory factors, increased IL-10 levels, and inhibited IL-33/ST2 axis expression, thereby inhibiting hypoxia-induced proliferation of pulmonary artery smooth muscle cells and ameliorating HPH.

人脐带间充质基质细胞衍生的外泌体可通过巨噬细胞缓解缺氧诱发的小鼠肺动脉高压。
肺动脉高压(PH)是一种顽固、严重和进行性的心肺疾病。最近的研究结果表明,人脐带间充质基质细胞(HUCMSCs)和HUCMSC衍生的外泌体(HUCMSC-Exos)对肺动脉高压具有潜在的治疗价值。然而,它们是否对缺氧性肺动脉高压(HPH)有益处尚不清楚。外泌体是细胞内多囊体与细胞膜融合后释放到细胞外环境中的,它们在细胞通讯中发挥着重要作用。Exos 可改善免疫炎症水平、改变巨噬细胞表型、调节线粒体代谢功能和抑制肺血管重塑,从而改善 PH。巨噬细胞是细胞因子和其他递质的重要来源,可促进细胞因子、血管活性分子和活性氧的释放,而所有这些都与肺血管重塑有关。因此,本研究旨在探讨 HUCMSC-Exos 是否能通过靶向巨噬细胞改善肺部炎症微环境并抑制肺血管重塑,同时找出其潜在机制。结果显示,HUCMSC-Exos能促进M2巨噬细胞极化,减少促炎因子,提高IL-10水平,抑制IL-33/ST2轴表达,从而抑制缺氧诱导的肺动脉平滑肌细胞增殖,改善HPH。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
STEM CELLS
STEM CELLS 医学-生物工程与应用微生物
CiteScore
10.30
自引率
1.90%
发文量
104
审稿时长
3 months
期刊介绍: STEM CELLS, a peer reviewed journal published monthly, provides a forum for prompt publication of original investigative papers and concise reviews. STEM CELLS is read and written by clinical and basic scientists whose expertise encompasses the rapidly expanding fields of stem and progenitor cell biology. STEM CELLS covers: Cancer Stem Cells, Embryonic Stem Cells/Induced Pluripotent Stem (iPS) Cells, Regenerative Medicine, Stem Cell Technology: Epigenetics, Genomics, Proteomics, and Metabonomics, Tissue-Specific Stem Cells, Translational and Clinical Research.
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