The European respiratory journal · 2025
Particulate matter-related ITIH4 deficiency is associated with an emphysema phenotype of COPD through JNK-dependent and JNK-independent signalling.
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Wu Sheng-Ming, Chen Kuan-Yuan, Chuang Hsiao-Chi, Ho Shu-Chuan, Lin Cheng-Wei, Han Chia-Li, Sun Wei-Lun, Feng Po-Hao, Lin Shiou-Fu, Chen Yueh-Hsi, Chen Tzu-Tao, Tseng Chien-Hua, Liu Wen-Te, Lee Kang-Yun
Аннотация
BACKGROUND: Prolonged exposure to airborne particulate matter (PM) is associated with emphysema and COPD; however, the precise underlying mechanism remains unclear. In a previous high-throughput screen, we identified inter-α-trypsin inhibitor heavy chain 4 (ITIH4) as a biomarker of long-term PM exposure. We hypothesised that ITIH4 is implicated in PM-related emphysema.
METHODS: We investigated the association between ITIH4 expression and ambient PM exposure through a clinical cohort analysis (220 patients with COPD and 61 healthy participants) and in vitro studies.
RESULTS: The COPD cohort studies revealed significant correlations between emphysema severity, ambient PM exposure and serum ITIH4 levels. In primary small airway epithelial cells from COPD patients with low basal levels of ITIH4, exposure to PM and oxidative stress led to increased apoptosis. However, ITIH4 overexpression significantly inhibited oxidative-stress-induced apoptosis in normal and COPD airway epithelial cells. Acute exposure to hydrogen peroxide resulted in the rapid degradation of ITIH4 protein with no effect on transcriptional level, although ITIH4 gene expression is downregulated in the lung tissue of patients with COPD. A human apoptosis antibody array revealed that ITIH4 overexpression attenuated hydrogen-peroxide-induced apoptotic signalling. Furthermore, extracellular ITIH4 protein confers cytoprotective functions in cells exposed to PM or oxidative stress. Mechanistically, ITIH4 attenuated oxidative-stress-induced c-Jun N-terminal kinase (JNK) activation and β-catenin decrease. A deficiency of ITIH4 exacerbated the effects of oxidative stress.
CONCLUSIONS: We identified a novel pathogenetic mechanism involving ITIH4, where chronic exposure to air pollution induces or promotes emphysema.
METHODS: We investigated the association between ITIH4 expression and ambient PM exposure through a clinical cohort analysis (220 patients with COPD and 61 healthy participants) and in vitro studies.
RESULTS: The COPD cohort studies revealed significant correlations between emphysema severity, ambient PM exposure and serum ITIH4 levels. In primary small airway epithelial cells from COPD patients with low basal levels of ITIH4, exposure to PM and oxidative stress led to increased apoptosis. However, ITIH4 overexpression significantly inhibited oxidative-stress-induced apoptosis in normal and COPD airway epithelial cells. Acute exposure to hydrogen peroxide resulted in the rapid degradation of ITIH4 protein with no effect on transcriptional level, although ITIH4 gene expression is downregulated in the lung tissue of patients with COPD. A human apoptosis antibody array revealed that ITIH4 overexpression attenuated hydrogen-peroxide-induced apoptotic signalling. Furthermore, extracellular ITIH4 protein confers cytoprotective functions in cells exposed to PM or oxidative stress. Mechanistically, ITIH4 attenuated oxidative-stress-induced c-Jun N-terminal kinase (JNK) activation and β-catenin decrease. A deficiency of ITIH4 exacerbated the effects of oxidative stress.
CONCLUSIONS: We identified a novel pathogenetic mechanism involving ITIH4, where chronic exposure to air pollution induces or promotes emphysema.