Cromolyn sodium reduces LPS-induced pulmonary fibrosis by inhibiting the EMT process enhanced by MC-derived IL-13.

IF 5.8 2区 医学 Q1 Medicine
Cheng Tan, Hang Zhou, Qiangfei Xiong, Xian Xian, Qiyuan Liu, Zexin Zhang, Jingjing Xu, Hao Yao
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引用次数: 0

Abstract

Background: Sepsis is a systemic inflammatory response caused by infection. When this inflammatory response spreads to the lungs, it can lead to acute lung injury (ALI) or more severe acute respiratory distress syndrome (ARDS). Pulmonary fibrosis is a potential complication of these conditions, and the early occurrence of pulmonary fibrosis is associated with a higher mortality rate. The underlying mechanism of ARDS-related pulmonary fibrosis remains unclear.

Methods: To evaluate the role of mast cell in sepsis-induced pulmonary fibrosis and elucidate its molecular mechanism. We investigated the level of mast cell and epithelial-mesenchymal transition(EMT) in LPS-induced mouse model and cellular model. We also explored the influence of cromolyn sodium and mast cell knockout on pulmonary fibrosis. Additionally, we explored the effect of MC-derived IL-13 on the EMT and illustrated the relationship between mast cell and pulmonary fibrosis.

Results: Mast cell was up-regulated in the lung tissues of the pulmonary fibrotic mouse model compared to control groups. Cromolyn sodium and mast cell knockout decreased the expression of EMT-related protein and IL-13, alleviated the symptoms of pulmonary fibrosis in vivo and in vitro. The PI3K/AKT/mTOR signaling was activated in fibrotic lung tissue, whereas Cromolyn sodium and mast cell knockout inhibited this pathway.

Conclusion: The expression level of mast cell is increased in fibrotic lungs. Cromolyn sodium intervention and mast cell knockout alleviate the symptoms of pulmonary fibrosis probably via the PI3K/AKT/mTOR signaling pathway. Therefore, mast cell inhibition is a potential therapeutic target for sepsis-induced pulmonary fibrosis.

色莫利钠通过抑制mc源性IL-13增强的EMT过程来减少lps诱导的肺纤维化。
背景:脓毒症是由感染引起的全身炎症反应。当这种炎症反应扩散到肺部时,可导致急性肺损伤(ALI)或更严重的急性呼吸窘迫综合征(ARDS)。肺纤维化是这些疾病的潜在并发症,肺纤维化的早期发生与较高的死亡率相关。ards相关肺纤维化的潜在机制尚不清楚。方法:探讨肥大细胞在脓毒症致肺纤维化中的作用,并阐明其分子机制。我们在lps诱导的小鼠模型和细胞模型中研究了肥大细胞和上皮间质转化(EMT)的水平。我们还探讨了色氨酸钠和肥大细胞敲除对肺纤维化的影响。此外,我们探讨了mc来源的IL-13对EMT的影响,并说明了肥大细胞与肺纤维化之间的关系。结果:与对照组相比,肺纤维化小鼠肺组织肥大细胞表达上调。色氨酸钠和肥大细胞敲除可降低emt相关蛋白和IL-13的表达,减轻体内和体外肺纤维化症状。PI3K/AKT/mTOR信号在纤维化肺组织中被激活,而色氨酸钠和肥大细胞敲除抑制了这一途径。结论:肥大细胞在纤维化肺组织中表达水平升高。色氨酸钠干预和肥大细胞敲除可能通过PI3K/AKT/mTOR信号通路缓解肺纤维化症状。因此,肥大细胞抑制是脓毒症诱导肺纤维化的潜在治疗靶点。
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来源期刊
Respiratory Research
Respiratory Research RESPIRATORY SYSTEM-
CiteScore
9.70
自引率
1.70%
发文量
314
审稿时长
4-8 weeks
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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