嗅觉外充质干细胞衍生的外泌体通过抑制Tfh细胞反应改善小鼠Sjögren综合征。

Ke Rui, Ziwei Shen, Na Peng, Futao Zhao, Yuan Tang, Shiyi Liu, Xinyi Xu, Chang Liu, Ling Wu, Jie Tian, Liwei Lu
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引用次数: 2

摘要

目的:探讨嗅觉外充质干细胞衍生外泌体(OE-MSC-Exos)对T滤泡辅助细胞(Tfh)应答的影响及其在实验性Sjögrens综合征(ESS)治疗中的意义。方法:用唾液腺(SG)蛋白免疫C57BL/6小鼠,建立小鼠ESS模型。在Tfh细胞极化条件下加入OE-MSC-Exos, FCM检测Tfh细胞比例。用小干扰RNA沉默OE-MSCs的PD-L1,提取siPD-L1-OE-MSC-Exos。结果:我们发现OE-MSC-Exos的转移显著减缓了ESS小鼠的疾病进展并降低了Tfh细胞的反应。在培养中,OE-MSC-Exos能有效抑制Tfh细胞向naïve T细胞的分化。此外,OE-MSC-Exos高水平表达程序性细胞死亡蛋白1 (PD-L1)配体,降低OE-MSC-Exos中PD-L1的表达,显著降低其体外抑制Tfh细胞分化的能力。一致地,PD-L1敲低的OE-MSC-Exos的转移在ESS小鼠中表现出显著降低的治疗效果,伴随着持续的Tfh细胞反应和高水平的自身抗体产生。结论:我们的研究结果表明OE-MSC-Exos可能通过pd - l1依赖的方式抑制Tfh细胞反应来发挥其改善ESS进展的治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Olfactory Ecto-mesenchymal Stem Cell-derived Exosomes Ameliorate Murine Sjögren's Syndrome via Suppressing Tfh Cell Response.

Olfactory Ecto-mesenchymal Stem Cell-derived Exosomes Ameliorate Murine Sjögren's Syndrome via Suppressing Tfh Cell Response.

Olfactory Ecto-mesenchymal Stem Cell-derived Exosomes Ameliorate Murine Sjögren's Syndrome via Suppressing Tfh Cell Response.

Olfactory Ecto-mesenchymal Stem Cell-derived Exosomes Ameliorate Murine Sjögren's Syndrome via Suppressing Tfh Cell Response.

Objectives: To investigate the effect of olfactory ecto-mesenchymal stem cell-derived exosomes (OE-MSC-Exos) on T follicular helper (Tfh) cell response and their implication in treating experimental Sjögrens syndrome (ESS).

Methods: C57BL/6 mice were immunized with salivary glands (SG) proteins to induce ESS mouse model. OE-MSC-Exos were added to the Tfh cell polarization condition, and the proportion of Tfh cells was detected by FCM. The PD-L1 of OE-MSCs was silenced with small interfering RNA to extract siPD-L1-OE-MSC-Exos.

Results: We found that transfer of OE-MSC-Exos markedly attenuated disease progression and reduced Tfh cell response in mice with ESS. In culture, OE-MSC-Exos potently inhibited the differentiation of Tfh cells from naïve T cells. Moreover, OE-MSC-Exos expressed high level of the ligand for the programmed cell death protein 1 (PD-L1), knocking down PD-L1 expression in OE-MSC-Exos significantly decreased their capacity to suppress Tfh cell differentiation in vitro. Consistently, transfer of OE-MSC-Exos with PD-L1 knockdown exhibited profoundly diminished therapeutic effect in ESS mice, accompanied with sustained Tfh cell response and high levels of autoantibody production.

Conclusion: Our results suggest that OE-MSC-Exos may exert their therapeutic effect in ameliorating ESS progression via suppressing Tfh cell response in a PD-L1-dependent manner.

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