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梓醇联合脂多糖通过 STAT3 信号通路诱导产生白细胞介素-10 的调节性 B 细胞。

Astilbin combined with lipopolysaccharide induces IL-10-producing regulatory B cells via the STAT3 signalling pathway.

机构信息

Department of Gastroenterology, Affiliated Hospital, Yangzhou University, Yangzhou 225001, PR China.

Jiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, Yangzhou, 225001, PR China.

出版信息

Biomed Pharmacother. 2020 Sep;129:110450. doi: 10.1016/j.biopha.2020.110450. Epub 2020 Jul 7.

Abstract

OBJECTIVES

Astilbin exerts immunoregulatory activities and plays anti-inflammatory effects in inflammation-associated diseases. IL-10-producing B cells are the major subset of regulatory B cells (Bregs) and inhibit inflammation and autoimmune diseases. This study aimed to analyse the inducing effect of astilbin on Bregs and investigate the involved molecular mechanisms.

METHODS

The frequencies and activities of IL-10-producing Bregs were observed using the co-treatment of astilbin and lipopolysaccharide (LPS) ex vivo. The protective effect of astilbin/LPS-induced Bregs on dextran sulphate sodium (DSS)-induced colitis was confirmed in vivo. The molecular signalling events of Breg induction were checked via Western blot. CD40 and toll-like receptor (TLR) 4 B cells were treated with astilbin/LPS to determine the modulatory role of CD40 or TLR4 on astilbin/LPS-induced Bregs.

RESULTS

Although astilbin alone could not affect Bregs, the co-treatment of astilbin and LPS remarkably induced CD19 CD1d and CD19 TIM-1 cells which produced IL-10 ex vivo. Colonic CD19 CD1d and CD19 TIM-1 cells were also increased in astilbin-treated mice with DSS-induced colitis. The adoptive transfer of CD19 TIM-1 cells pre-induced by astilbin/LPS directly suppressed the progression of DSS-induced colitis. Combined astilbin and LPS stimulated the STAT3 activation of CD19 TIM-1 cells but had no effects on SOCS3, AKT, NF-κB, Erk, JNK nor P38. Inhibiting the STAT3 phosphorylation of CD19 TIM-1 cells abolished Breg induction by astilbin/LPS. Furthermore, Breg induction was weakened in CD40 B cells with the decrease in STAT3 activation, but had disappeared in TLR4 B cells with no STAT3 activation, thereby confirming the indispensable role of TLR4 signalling in the induction of IL-10-producing Bregs.

CONCLUSIONS

This study reports the new immunoregulatory role of astilbin for promoting IL-10-producing B cells and suggests the possible use of astilbin in the therapy of inflammatory diseases.

摘要

目的

紫云英苷具有免疫调节活性,并在炎症相关疾病中发挥抗炎作用。产生白细胞介素 10 的 B 细胞是调节性 B 细胞(Bregs)的主要亚群,可抑制炎症和自身免疫性疾病。本研究旨在分析紫云英苷对 Bregs 的诱导作用,并探讨其相关的分子机制。

方法

采用紫云英苷与脂多糖(LPS)体外共处理的方法,观察 IL-10 产生的 Bregs 的频率和活性。体内实验证实了紫云英苷/LPS 诱导的 Bregs 对葡聚糖硫酸钠(DSS)诱导的结肠炎的保护作用。通过 Western blot 检查 Breg 诱导的分子信号事件。用紫云英苷/LPS 处理 CD40 和 Toll 样受体(TLR)4 B 细胞,以确定 CD40 或 TLR4 对紫云英苷/LPS 诱导的 Bregs 的调节作用。

结果

虽然紫云英苷单独作用不能影响 Bregs,但与 LPS 共同处理可显著诱导 CD19 CD1d 和 CD19 TIM-1 细胞体外产生白细胞介素 10。在 DSS 诱导的结肠炎的紫云英苷处理小鼠中,结肠 CD19 CD1d 和 CD19 TIM-1 细胞也增加。预先用紫云英苷/LPS 诱导的 CD19 TIM-1 细胞的过继转移直接抑制了 DSS 诱导的结肠炎的进展。联合紫云英苷和 LPS 刺激 CD19 TIM-1 细胞的 STAT3 激活,但对 SOCS3、AKT、NF-κB、Erk、JNK 和 P38 没有影响。抑制 CD19 TIM-1 细胞的 STAT3 磷酸化可消除紫云英苷/LPS 诱导的 Breg。此外,在 STAT3 激活减少的 CD40 B 细胞中,Breg 诱导作用减弱,但在没有 STAT3 激活的 TLR4 B 细胞中消失,从而证实了 TLR4 信号在诱导产生白细胞介素 10 的 Bregs 中的不可或缺作用。

结论

本研究报告了紫云英苷促进白细胞介素 10 产生的 B 细胞的新免疫调节作用,并提示紫云英苷在炎症性疾病治疗中的可能应用。

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