Yudong Liu, Jingxian Li, Zhenyu Wu, Shiyu Wu, Xinwei Yang
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引用次数: 0
摘要
成纤维细胞生长因子21 (FGF21)在一系列病理条件下调节炎症反应。然而,FGF21是否调节哮喘仍未研究。本研究试图通过卵清蛋白(OVA)诱导的小鼠模型来研究其在哮喘中的作用。在出现哮喘症状的小鼠中观察到FGF21水平升高。与野生型(WT)小鼠相比,FGF21敲除(KO)小鼠表现出加重的哮喘病理,其特征是炎症细胞浸润增加,炎症细胞因子释放增加。腺相关病毒(AAV)介导的FGF21过表达显著逆转了WT和FGF21 KO小鼠的哮喘病理。在WT小鼠中观察到卵细胞攻击后激活的NLRP3炎性体,并且这种反应在FGF21 KO小鼠中增强,表现为NLRP3、ASC、裂解Caspase-1、裂解Gasdermin D (GSDMD)、IL-1β和IL-18的上调。药理学抑制NLRP3可改善FGF21 KO小鼠在卵细胞攻击后的加重哮喘病理。总的来说,目前的研究强调了FGF21在哮喘发病机制中的关键作用,并表明FGF21可以作为治疗干预的潜在靶点。
Fibroblast Growth Factor 21 Confers Protection Against Asthma Through Inhibition of NLRP3 Inflammasome Activation.
Fibroblast growth factor 21 (FGF21) modulates the inflammatory response in a range of pathological conditions. However, whether FGF21 modulates asthma remains unexplored. This study sought to investigate its function in asthma using an ovalbumin (OVA)-induced mouse model. Levels of FGF21 were observed to be elevated in mice exhibiting asthmatic symptoms. FGF21 knockout (KO) mice exhibited exacerbated asthmatic pathologies, marked by heightened infiltration of inflammatory cells and elevated release of inflammatory cytokine, compared to wild-type (WT) mice with OVA challenge. Adeno-associated virus (AAV)-mediated overexpression of FGF21 significantly reversed asthmatic pathologies in both WT and FGF21 KO mice. Activated NLRP3 inflammasome was observed in WT mice following OVA challenge, and this response was intensified in FGF21 KO mice, manifested by an upregulation of NLRP3, ASC, cleaved Caspase-1, cleaved Gasdermin D (GSDMD), IL-1β, and IL-18. Pharmacological suppression of NLRP3 ameliorated the aggravated asthmatic pathologies observed in FGF21 KO mice after OVA challenge. Overall, the present work underscores the pivotal function of FGF21 in the pathogenesis of asthma and suggests that FGF21 could serve as a potential target for therapeutic interventions.
期刊介绍:
Inflammation publishes the latest international advances in experimental and clinical research on the physiology, biochemistry, cell biology, and pharmacology of inflammation. Contributions include full-length scientific reports, short definitive articles, and papers from meetings and symposia proceedings. The journal''s coverage includes acute and chronic inflammation; mediators of inflammation; mechanisms of tissue injury and cytotoxicity; pharmacology of inflammation; and clinical studies of inflammation and its modification.