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胸腺基质淋巴细胞生成素处理的树突状细胞来源的外泌体通过 miR-21/Smad7 轴调节辅助性 T 细胞 17/调节性 T 细胞分化。

Exosomes derived from thymic stromal lymphopoietin-treated dendritic cells regulate T helper 17/regulatory T cell differentiation via miR-21/Smad7 axis.

机构信息

Department of ophthalmology, The First Affiliated Hospital of USTC, Division of life sciences and medicine, University of Science and Technology of China, No. 17, Lujiang Road, Hefei, 230001, Anhui, China.

Department of ophthalmology, Saarland University Medical Center, Kirrberger Strasse 100 Geb. 22, 66421, Homburg, Saarland, Germany.

出版信息

Exp Cell Res. 2021 Jan 1;398(1):112393. doi: 10.1016/j.yexcr.2020.112393. Epub 2020 Nov 28.

Abstract

Thymic stromal lymphopoietin (TSLP) is associated with fungal keratitis. This work aims to investigate whether TSLP can regulate T helper (Th) 17 and regulatory T cell (Treg) differentiation. We separated dendritic cells (DCs) from peripheral blood of healthy volunteers. DCs were treated with TSLP to activate DCs, and exosomes were obtained. CD T cells were incubated with exosomes from TSLP-treated DCs. We found that exosomes from TSLP-treated DCs notably promoted the proportions of Th17 cells and inhibited the proportions of Tregs in the CD4 T cells. Moreover, exosomes from TSLP-treated DCs enhanced the expression of retinoid-related orphan receptor γt (RORγt) and interleukin 17 (IL-17), and repressed the expression of forkhead box protein P3 (Foxp3) and interleukin 10 (IL-10) in the CD4 T cells. Furthermore, miR-21 was highly expressed in exosomes from TSLP-treated DCs. Exosomes from TSLP-treated miR-21-silenced DCs promoted Treg differentiation and suppressed Th17 differentiation. Smad7 up-regulation repressed Th17 differentiation and enhanced Treg differentiation, which was abolished by miR-21 overexpression. Smad7 overexpression rescued the effect of exosomes from TSLP-treated DCs on Th17/Treg differentiation. In conclusion, our article confirms that TSLP induces DCs to deliver miR-21 by secreting exosomes, and thus miR-21 regulates Th17/Treg differentiation by inhibiting Smad7. Thus, this work further reveals the biological role of miR-21 in fungal keratitis.

摘要

胸腺基质淋巴细胞生成素(TSLP)与真菌性角膜炎有关。本研究旨在探讨 TSLP 是否能调节辅助性 T 细胞(Th)17 和调节性 T 细胞(Treg)分化。我们从健康志愿者外周血中分离树突状细胞(DC)。用 TSLP 处理 DC 以激活 DC,并获得外泌体。将 CD T 细胞与 TSLP 处理的 DC 来源的外泌体共孵育。结果发现,TSLP 处理的 DC 来源的外泌体显著促进了 CD4 T 细胞中 Th17 细胞的比例,并抑制了 Treg 的比例。此外,TSLP 处理的 DC 来源的外泌体增强了 CD4 T 细胞中视黄酸相关孤儿受体 γt(RORγt)和白细胞介素 17(IL-17)的表达,抑制了叉头框蛋白 P3(Foxp3)和白细胞介素 10(IL-10)的表达。此外,miR-21 在 TSLP 处理的 DC 来源的外泌体中高度表达。来自 TSLP 处理的 miR-21 沉默的 DC 的外泌体促进 Treg 分化并抑制 Th17 分化。Smad7 的上调抑制了 Th17 分化并增强了 Treg 分化,而 miR-21 的过表达则消除了这种作用。Smad7 的过表达挽救了 TSLP 处理的 DC 来源的外泌体对 Th17/Treg 分化的影响。综上所述,本研究证实 TSLP 通过分泌外泌体诱导 DC 释放 miR-21,从而通过抑制 Smad7 调节 Th17/Treg 分化。因此,本研究进一步揭示了 miR-21 在真菌性角膜炎中的生物学作用。

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