间充质干细胞来源的外泌体抑制刺激1- orai1信号和钙超载诱导的狼疮滤泡辅助性T细胞线粒体损伤

IF 9.6 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2025-09-22 eCollection Date: 2025-01-01 DOI:10.34133/bmr.0255
Yingyu Wang, Qingyong Xiang, Yueren Wu, Xiaoyun Zhang, Zhongzhou Huang, Yunxia Hou, Yan Wang, Ji Yang, Weiguo Wan, Hejian Zou, Xue Yang
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种以异常T细胞活性和过量自身抗体产生为特征的自身免疫性疾病。滤泡辅助性T细胞(Tfh)在促进B细胞介导的自身抗体产生中起关键作用,促进SLE的进展。尽管间充质干细胞衍生外泌体(MSC-Exos)具有免疫调节特性,但其对SLE中Tfh的影响及其潜在机制尚不清楚。为了解决这个问题,我们首先分析了从吡喹莫德诱导的狼疮小鼠模型(IMQ-SLE)中分类的Tfh,发现MSC-Exos有效抑制Tfh功能。与此一致,Tfh极化实验表明MSC-Exos在体外调节Tfh分化。随后,我们评估了静脉注射MSC-Exos的治疗潜力,并证实MSC-Exos在体内显著抑制Tfh的扩增和功能。进一步的RNA测序和验证实验表明,MSC-Exos可以恢复Tfh中钙的稳态。机制上,MSC-Exos下调基质相互作用分子1 (Stim1)和Orai1的表达,抑制活化T细胞核因子(NFAT)和核因子κB (NF-κB)的活化。同时,MSC-Exos通过抑制线粒体钙单转运蛋白(MCU)的表达来减轻钙超载引起的线粒体损伤。最后,我们观察到MSC-Exos在体内和体外都能促进滤泡调节性T细胞(Tfr)的分化。这些发现表明,MSC-Exos通过纠正Tfh中的细胞钙失调和线粒体损伤来改善SLE,同时恢复Tfh/Tfr失衡,突出了它们作为SLE治疗策略的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesenchymal Stem Cell-Derived Exosomes Inhibit Stim1-Orai1 Signaling and Calcium Overload-Induced Mitochondrial Damage of Follicular Helper T Cells in Lupus.

Systemic lupus erythematosus (SLE) is an autoimmune disorder characterized by aberrant T cell activity and excessive autoantibody production. Follicular helper T cells (Tfh) play a pivotal role in promoting B cell-mediated autoantibody generation, contributing to SLE progression. Although mesenchymal stem cell-derived exosomes (MSC-Exos) exhibit immunomodulatory properties, their effects on Tfh in SLE and the underlying mechanisms remain unclear. To address this, we first analyzed sorted Tfh from an imiquimod-induced lupus murine model (IMQ-SLE) and found that MSC-Exos effectively suppressed Tfh function. Consistently, Tfh polarization assays demonstrated that MSC-Exos modulate Tfh differentiation in vitro. Subsequently, we evaluated the therapeutic potential of intravenous MSC-Exos administration and confirmed that MSC-Exos markedly inhibited Tfh expansion and function in vivo. Further RNA sequencing followed by validation experiments identified that MSC-Exos restore calcium homeostasis in Tfh. Mechanically, MSC-Exos down-regulate stromal interaction molecule 1 (Stim1) and Orai1 expression, inhibiting nuclear factor of activated T cells (NFAT) and nuclear factor κB (NF-κB) activation. In parallel, MSC-Exos mitigate calcium overload-induced mitochondrial damage by suppressing mitochondrial calcium uniporter (MCU) expression. Finally, we observed that MSC-Exos also promote the differentiation of follicular regulatory T cells (Tfr) both in vivo and in vitro. These findings suggest that MSC-Exos ameliorate SLE by correcting cellular calcium dysregulation and mitochondrial damage in Tfh while simultaneously restoring the Tfh/Tfr imbalance, highlighting their potential as a therapeutic strategy for SLE.

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