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

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

Abstract

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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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。
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。
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