Effects of PM2.5 exposure on the Notch signaling pathway and immune imbalance in chronic obstructive pulmonary disease

• Published in: Environmental pollution (1987) Vol. 226; pp. 163 - 173
• Main Authors: Gu, Xing-yu, Chu, Xu, Zeng, Xiao-Li, Bao, Hai-Rong, Liu, Xiao-Ju
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.07.2017
• Subjects: Adaptive immunity; Air Pollutants - toxicity; Animals; Humans; Interleukin-10 - metabolism; Interleukin-17 - metabolism; Mice; Notch signaling; Particulate Matter - toxicity; PM2.5; Pulmonary disease, Chronic obstructive; Pulmonary Disease, Chronic Obstructive - immunology; Pulmonary Disease, Chronic Obstructive - metabolism; Receptors, Notch - metabolism; RNA, Messenger - metabolism; Signal Transduction; Smoke; T lymphocytes subset; T-Lymphocytes, Regulatory; Th17 Cells; Adaptive immunity; T lymphocytes subset; Notch signaling; PM2.5; Pulmonary disease, Chronic obstructive
• ISSN: 0269-7491; 1873-6424
• DOI: 10.1016/j.envpol.2017.03.070

Chronic Obstructive Pulmonary Disease (COPD) is associated with T lymphocytes subset (Th1/Th2, Th17/Treg) imbalance. Notch signaling pathway plays a key role in the development of the adaptive immunity. The immune disorder induced by fine particulate matter (PM2.5) is related to COPD. The aim of this study was to investigate the mechanism by which PM2.5 influences the Notch signaling pathway leading to worsening immune disorder and accelerating COPD development. A COPD mouse model was established by cigarette smoke exposure. PM2.5 exposure was performed by aerosol inhalation. γ-secretase inhibitor (GSI) was given using intraperitoneal injection. Splenic T lymphocytes were purified using a density gradient centrifugation method. CD4+ T lymphocyte subsets (Th1/Th2, Th17/Treg) were detected using flow cytometry. mRNA and proteins of Notch1/2/3/4, Hes1/5, and Hey1 were detected using RT-PCR and Western blot. Serum INF-γ, IL-4, IL-17 and IL-10 concentrations were measured using ELISA. The results showed that in COPD mice Th1% and Th17%, Th1/Th2 and Th17/Treg were increased, and the levels of mRNA and protein in Notch1/2/3/4, Hes1/5, and Hey1 and serum INF-γ and IL-17 concentrations were significantly increased, and Th2%, Treg%, and serum IL-4 and IL-10 concentrations were significantly decreased. COPD Mice have Th1- and Th17-mediated immune disorder, and the Notch signaling pathway is in an overactivated state. PM2.5 promotes the overactivation of the Notch signaling pathway and aggravates the immune disorder of COPD. GSI can partially inhibit the activation of the Notch signaling pathway and alleviate the immune disorder under basal state and the immune disorder of COPD caused by PM2.5. This result suggests that PM2.5 is involved in the immune disorder of mice with COPD by affecting the Notch signaling pathway and that PM2.5 aggravates COPD. [Display omitted] •The COPD mice demonstrated Th1 and Th17 dominant immune imbalance.•PM2.5 aggravates the Th1/Th2 and Th17/Treg immune imbalance in COPD mice.•The Notch pathway regulates T cell differentiation and participates in the immune imbalance in the pathogenesis of COPD.•PM2.5 can promote the activation of the Notch pathway while GSI can block this pathway's activation partially. This study suggests that PM2.5 causes immune dysfunction via Notch signaling pathway, which is involved in the pathogenesis of COPD.