Deng Ya, Zhao Jiaying, Gong Chen, Ding Wenqian, Fang Lulu, Liu Huaqing, Li Ming, Shen Bing, Ding Shenggang
Department of Pediatrics, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Department of Pediatrics, The Second Affiliated Hospital of Anhui Medical University, Hefei, China.
JCI Insight. 2025 May 8;10(11). doi: 10.1172/jci.insight.185975. eCollection 2025 Jun 9.
Airway smooth muscle (ASM) hyperplasia is a hallmark of airway remodeling in asthma, which still lacks an effective treatment. Low-density lipoprotein receptor-related protein 1 (LRP1) is involved in regulating the proliferation of various cell types, and the intracellular domain of LRP1 (LRP1-ICD) also exhibits unique biological functions. However, the role of LRP1 in asthma airway remodeling remains unclear. In the present study, LRP1 was increased in ASM cells of mice with OVA-induced chronic asthma, with the elevation in LRP1-ICD protein levels being significantly greater than that of the LRP1 β chain. In vivo experiments demonstrated that inhibiting LRP1 reduced ASM proliferation in these mice. Mechanistically, LRP1 knockdown inhibited the FGF2/ERK signaling pathway, thereby arresting cell cycle progression and suppressing ASM cell proliferation. Additionally, in vitro experiments revealed that the inhibitory effect of LRP1-ICD overexpression on ASM cell proliferation was lost after adjusting the levels of LRP1. LRP1-ICD overexpression inhibited full-length LRP1 protein levels by promoting its protein degradation rather than by suppressing its transcription, thus preventing further exacerbation of asthma. In conclusion, this study clarifies the molecular biological mechanism by which LRP1 regulates ASM proliferation, suggesting targeting full-length LRP1 as a strategy for therapeutic intervention in asthma airway remodeling.
气道平滑肌(ASM)增生是哮喘气道重塑的一个标志,目前仍缺乏有效的治疗方法。低密度脂蛋白受体相关蛋白1(LRP1)参与调节多种细胞类型的增殖,LRP1的细胞内结构域(LRP1-ICD)也具有独特的生物学功能。然而,LRP1在哮喘气道重塑中的作用仍不清楚。在本研究中,卵清蛋白(OVA)诱导的慢性哮喘小鼠的ASM细胞中LRP1增加,LRP1-ICD蛋白水平的升高显著大于LRP1β链。体内实验表明,抑制LRP1可减少这些小鼠的ASM增殖。机制上,敲低LRP1可抑制FGF2/ERK信号通路,从而阻止细胞周期进程并抑制ASM细胞增殖。此外,体外实验表明,在调整LRP1水平后,LRP1-ICD过表达对ASM细胞增殖的抑制作用消失。LRP1-ICD过表达通过促进全长LRP1蛋白降解而不是抑制其转录来抑制全长LRP1蛋白水平,从而防止哮喘进一步加重。总之,本研究阐明了LRP1调节ASM增殖的分子生物学机制,提示靶向全长LRP1作为哮喘气道重塑治疗干预的策略。