IFN-γ和IL-1β诱导间充质干细胞通过增强归巢效应和免疫调节改善急性呼吸窘迫综合征

IF 3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Biomolecules & Therapeutics Pub Date : 2025-03-01 Epub Date: 2025-02-20 DOI:10.4062/biomolther.2025.004
Taeho Kong, Su Kyoung Seo, Yong-Seok Han, Woo Min Seo, Bokyong Kim, Jieun Kim, Young-Jae Cho, Seunghee Lee, Kyung-Sun Kang
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引用次数: 0

摘要

急性呼吸窘迫综合征(ARDS)是一种以广泛的肺部炎症和肺泡毛细血管通透性增加为特征的严重疾病,通常由感染或全身炎症反应引发。基于间充质干细胞(MSCs)的治疗有望治疗ARDS,因为MSCs具有免疫调节和再生特性,可以减轻炎症并增强组织修复。与初始MSCs相比,经过修饰以增强特定功能的引物MSCs在靶向治疗中表现出优越的治疗效果。本研究通过混合淋巴细胞反应(MLR)实验和与M1/M2巨噬细胞共培养实验探讨MSCs的免疫调节潜能。此外,RNA测序用于鉴定引物间充质干细胞中免疫和炎症相关因子的变化。在lps诱导的ARDS小鼠模型中评估了MSCs的治疗效果,并通过空间转录组学分析探讨了其潜在机制。研究发现,与未处理的MSCs相比,IFN-γ和IL-1β诱导的MSCs显著增强了对T细胞活性的抑制,同时抑制TNF-α,增加巨噬细胞中IL-10的产生。值得注意的是,这两种细胞因子的联合治疗导致免疫和炎症调节因子的显著上调。此外,我们的分析阐明了MSCs治疗作用的机制,包括抑制肺组织中炎症细胞的浸润,调节免疫和炎症反应,增强弹性蛋白纤维的形成。信号通路分析证实通过调节NFκB和TNF-α信号通路可增强疗效。总之,在早期ARDS中,引物MSCs表现出增强的归巢能力,改善肺功能,减少炎症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primed Mesenchymal Stem Cells by IFN-γ and IL-1β Ameliorate Acute Respiratory Distress Syndrome through Enhancing Homing Effect and Immunomodulation.

Acute Respiratory Distress Syndrome (ARDS) is a severe condition characterized by extensive lung inflammation and increased alveolar-capillary permeability, often triggered by infections or systemic inflammatory responses. Mesenchymal stem cells (MSCs)-based therapy holds promise for treating ARDS, as MSCs manifest immunomodulatory and regenerative properties that mitigate inflammation and enhance tissue repair. Primed MSCs, modified to augment specific functionalities, demonstrate superior therapeutic efficacy in targeted therapies compared to naive MSCs. This study explored the immunomodulatory potential of MSCs using mixed lymphocyte reaction (MLR) assays and co-culture experiments with M1/M2 macrophages. Additionally, RNA sequencing was employed to identify alterations in immune and inflammation-related factors in primed MSCs. The therapeutic effects of primed MSCs were assessed in an LPS-induced ARDS mouse model, and the underlying mechanisms were investigated through spatial transcriptomics analysis. The study revealed that MSCs primed with IFN-γ and IL-1β significantly enhanced the suppression of T cell activity compared to naive MSCs, concurrently inhibiting TNF-α while increasing IL-10 production in macrophages. Notably, combined treatment with these two cytokines resulted in a significant upregulation of immune and inflammation-regulating factors. Furthermore, our analyses elucidated the mechanisms behind the therapeutic effects of primed MSCs, including the inhibition of inflammatory cell infiltration in lung tissue, modulation of immune and inflammatory responses, and enhancement of elastin fiber formation. Signaling pathway analysis confirmed that efficacy could be enhanced by modulating NFκB and TNF-α signaling. In conclusion, in early-phase ARDS, primed MSCs displayed enhanced homing capabilities, improved lung function, and reduced inflammation.

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来源期刊
CiteScore
6.60
自引率
8.10%
发文量
72
审稿时长
6-12 weeks
期刊介绍: Biomolecules & Therapeutics (Biomolecules & Therapeutics) (Print ISSN 1976-9148, Online ISSN 2005-4483) is an international, peer-reviewed, open access journal that covers pharmacological and toxicological fields related to bioactive molecules and therapeutics. It was launched in 1993 as "The Journal of Applied Pharmacology (ISSN 1225-6110)", and renamed "Biomolecules & Therapeutics" (Biomol Ther: abbreviated form) in 2008 (Volume 16, No. 1). It is published bimonthly in January, March, May, July, September and November. All manuscripts should be creative, informative, and contribute to the development of new drugs. Articles in the following categories are published: review articles and research articles.
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