RAR相关孤儿受体γ
哮喘
车站3
炎症
气道
免疫学
细胞
医学
化学
细胞生物学
生物
信号转导
免疫系统
生物化学
麻醉
FOXP3型
作者
Lijie Wang,Jiabo Yuan,Ruiqi Zhao,Congyao Wang,Zhuying Li
标识
DOI:10.1080/08820139.2025.2450239
摘要
INTRODUCTION: T helper 17 (Th17) cells have a significant effect in the pathogenesis of asthma, and signal transducer and activator of transcription 3 (STAT3) pathway activation is critical for Th17 cell differentiation. Timosaponin A-III (TA3) was reported to inhibit the STAT3 pathway. Here, we investigated whether TA3 improved asthma by inhibiting the STAT3 pathway. METHODS: T cells were triggered for Th17 differentiation, and TA3 (5 or 10 μM) was used to treat cells during induction of Th17 differentiation. RESULTS: experiments. Compared to positive control static (a specific inhibitor of STAT3), TA3 had a similar effect on Th17 differentiation. DISCUSSION: These findings indicate that TA3 may ameliorate Th17 cell differentiation by suppressing STAT3/RORγt signaling. Our data provide evidence of the potential benefits of TA3 for the treatment of asthma.
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