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基于 TMT 的定量蛋白质组学揭示 SLC3A2 和 ATP1A3 表达的抑制有助于针刺在卵清蛋白诱导的小鼠哮喘模型中对气道炎症的抑制作用。

TMT-based quantitative proteomics reveals suppression of SLC3A2 and ATP1A3 expression contributes to the inhibitory role of acupuncture on airway inflammation in an OVA-induced mouse asthma model.

机构信息

Department of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, China; Institutes of Integrative Medicine, Fudan University, Shanghai, China.

Gumei community Health center of Minhang district of Shanghai, Shanghai, China.

出版信息

Biomed Pharmacother. 2021 Feb;134:111001. doi: 10.1016/j.biopha.2020.111001. Epub 2020 Dec 16.

DOI:10.1016/j.biopha.2020.111001
PMID:33341053
Abstract

Asthma is a chronic airway inflammatory disease and acupuncture is frequently used in patients suffering from asthma in clinic. However, the regulatory mechanism of acupuncture treatment in asthma is not fully elucidated. We sought to investigate the effectiveness of acupuncture on asthma and the associated regulatory mechanism. An ovalbumin (OVA)-induced mouse asthma model was established and the effect of acupuncture on airway hyperresponsiveness (AHR), mucus hypersecretion and inflammation was assessed. Tandem mass tag (TMT)-based quantitative proteomics analysis of lung tissue and bioinformatics analysis were performed. Our results revealed that the OVA-induced mouse asthma model was successfully established with the significantly elevated AHR to methacholine (Mch), and acupuncture was effective in attenuation of AHR to Mch, peribronchial and perivascular inflammation and mucus production. The inflammatory cells around the airways, mucous secretion as well as levels of IgE, CCL5, CCL11, IL-17A in bronchoalveolar lavage fluid (BALF) and IL-4, IL-5 and IL-13 levels in serum were siginificantly inhibited by acupuncture. TMT-based quantitative proteomics analysis found that a total of 6078 quantifiable proteins were identified, and 564 (334 up-regulated and 230 down regulated) differentially expressed proteins (DEPs) were identified in OVA-induced asthma model group (A) versus normal control group (NC). Acupuncture treatment resulted in 667 DEPs (416 up-regulated and 251 down regulated) compared with A group, and 86 overlapping DEPs were identified in NC, A and AA groups. Among the 86 overlapping DEPs, we identified 41 DEPs regulated by acupuncture. Based on the above data, we performed a systematic bioinformatics analysis of the 41 DEPs, and results showed that these 41 DEPs were predominantly related to 4 KEGG pathways including SNARE interactions in vesicular transport, ferroptosis, endocrine and other factor-regulated calcium reabsorption, and protein digestion and absorption. DEPs of SLC3A2 and ATP1A3 expression levels were verified by immumohistochemical staining. Mice in OVA-induced asthma model group had elevated SLC3A2 and ATP1A3 expression and acupuncture had the ability to downregulate SLC3A2 and ATP1A3 protein expression. Furthermore, acupuncture reduced the MDA level and increased the GSH and SOD levels in the lung tissue. Taken together, our data suggested that acupuncture was effective in treating asthma by attenuation of AHR, mucus secretion and airway inflammation, and the mechanism was associated with regulation of ferroptosis, SLC3A2 and ATP1A3 protein expression as well as oxidative stress. Results from our experiments revealed the anti-inflammatory effect of acupuncture in OVA-induced mouse asthma model, leading to a more effective approach to be chosen by patients in clinic.

摘要

哮喘是一种慢性气道炎症性疾病,临床上常采用针刺疗法治疗哮喘患者。然而,针刺治疗哮喘的调控机制尚未完全阐明。我们旨在研究针刺治疗哮喘的疗效及其相关调控机制。建立卵清蛋白(OVA)诱导的小鼠哮喘模型,评估针刺对气道高反应性(AHR)、粘液分泌过度和炎症的影响。对肺组织进行串联质量标签(TMT)定量蛋白质组学分析和生物信息学分析。结果显示,OVA 诱导的小鼠哮喘模型成功建立,气道对乙酰甲胆碱(Mch)的反应性明显升高,针刺可有效减轻 Mch 诱导的 AHR、气道周围和血管周围炎症以及粘液分泌。针刺还显著抑制气道周围炎性细胞浸润、支气管肺泡灌洗液(BALF)中 IgE、CCL5、CCL11、IL-17A 以及血清中 IL-4、IL-5 和 IL-13 水平。TMT 定量蛋白质组学分析共鉴定到 6078 个可定量蛋白,OVA 诱导的哮喘模型组(A 组)与正常对照组(NC 组)比较,鉴定到 564 个差异表达蛋白(DEPs)(334 个上调,230 个下调)。与 A 组相比,针刺治疗组有 667 个 DEPs(416 个上调,251 个下调),NC、A 和 AA 组有 86 个重叠 DEPs。在 86 个重叠 DEPs 中,我们鉴定到 41 个受针刺调节的 DEPs。基于上述数据,我们对 41 个 DEPs 进行了系统的生物信息学分析,结果表明,这些 DEPs 主要与 SNARE 相互作用在囊泡运输、铁死亡、内分泌和其他因子调节的钙重吸收以及蛋白质消化和吸收等 4 个 KEGG 途径有关。通过免疫组织化学染色验证 SLC3A2 和 ATP1A3 的 DEPs 表达水平。OVA 诱导的哮喘模型组中 SLC3A2 和 ATP1A3 的表达升高,针刺能够下调 SLC3A2 和 ATP1A3 蛋白表达。此外,针刺还降低了肺组织中的 MDA 水平,增加了 GSH 和 SOD 水平。综上所述,针刺治疗哮喘的疗效与减轻 AHR、粘液分泌和气道炎症有关,其机制与铁死亡、SLC3A2 和 ATP1A3 蛋白表达以及氧化应激的调节有关。我们的实验结果揭示了针刺在 OVA 诱导的小鼠哮喘模型中的抗炎作用,为临床患者提供了更有效的治疗选择。

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