Katsumata Megumi, Ikari Jun, Urano Akira, Suzuki Eiko, Kugou Kazuto, Hasegawa Yoshinori, Tatsumi Koichiro, Suzuki Takuji
Department of Respirology, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan.
Department of Applied Genomics, Kazusa DNA Research Institute, Kisarazu 292-0818, Japan.
Int J Mol Sci. 2025 Jun 11;26(12):5573. doi: 10.3390/ijms26125573.
Neutrophil extracellular traps (NETs) are associated with the extracellular release of nuclear chromatin decorated with cytoplasmic proteins. Excessive release of NETs has been reported in chronic lung diseases, including chronic obstructive pulmonary disease (COPD). However, the role of NETs in the pathogenesis of COPD remains unclear. Peptidylarginine deaminase 4 (PAD4) contributes to NET formation. Therefore, in an elastase (ELS)-induced emphysema mouse model, we examined the role of PAD4 using gene knockout (KO) mice. First, we confirmed that ELS induced NET formation in the parenchyma of the lungs. PAD4 deficiency suppressed ELS-induced NET expression and tended to ameliorate the lung tissue injury. The cellular profile of bronchoalveolar lavage fluid (BALF) did not differ between the two groups. Additionally, PAD4 deficiency ameliorated emphysema and apoptosis in lung cells. Finally, we examined the effects of PAD4 on comprehensive gene expression signatures using RNA sequencing. Enrichment analysis of the transcriptomic data revealed that the expression of several genes associated with COPD pathogenesis was altered in the KO mice. Overall, the results suggest that PAD4 deficiency improves NET formation and emphysema in the lungs; this pathway can be a potential therapeutic target for the treatment of COPD.
中性粒细胞胞外诱捕网(NETs)与装饰有细胞质蛋白的核染色质的胞外释放有关。据报道,在包括慢性阻塞性肺疾病(COPD)在内的慢性肺部疾病中,NETs会过度释放。然而,NETs在COPD发病机制中的作用仍不清楚。肽基精氨酸脱氨酶4(PAD4)有助于NET的形成。因此,在弹性蛋白酶(ELS)诱导的肺气肿小鼠模型中,我们使用基因敲除(KO)小鼠研究了PAD4的作用。首先,我们证实ELS诱导了肺实质中NET的形成。PAD4缺陷抑制了ELS诱导的NET表达,并倾向于改善肺组织损伤。两组之间支气管肺泡灌洗液(BALF)的细胞谱没有差异。此外,PAD4缺陷改善了肺气肿和肺细胞凋亡。最后,我们使用RNA测序研究了PAD4对综合基因表达特征的影响。转录组数据的富集分析表明,KO小鼠中与COPD发病机制相关的几个基因的表达发生了改变。总体而言,结果表明PAD4缺陷可改善肺部NET的形成和肺气肿;这一途径可能是治疗COPD的潜在治疗靶点。