Effect of PM10 on pulmonary immune response and fetus development. (15th March 2021)

• Record Type: Journal Article
• Authors: Park, Eun-Jung; Yoon, Cheolho; Han, Ji-Seok; Lee, Gwang-Hee; Kim, Dong-Wan; Park, Eun-Jun; Lim, Hyun-Ji; Kang, Min-Sung; Han, Hyoung-Yun; Seol, Hyun-Joo; Kim, Kwang Pyo
• Is Part Of: Toxicology letters. Volume 339(2021)
• Page Start: 1
• Page End: 11
• Publication Date: 2021-03-15
• Subjects: Air pollution -- Particulate materials -- Lung inflammation -- Interferon gamma -- Hypoxia -- Stillbirth; Toxicology -- Periodicals; 363.179
• DOI: 10.1016/j.toxlet.2020.11.024
• Languages: English
• ISSNs: 0378-4274

Abstract

Graphical abstract: Highlights: PM10 was characterized PM10 and instilled intratracheally to male and female mice. PM10 induced dose-dependent inflammatory response followed by pathological lesions. PM10 exposure seemed to affect to the reproductive toxicity-related endpoints. Stillbirth was observed in three mice among eight dams exposed to the maximum dose. Expression of hypoxia-related proteins was altered in the lung tissues and cells. Abstract: Despite numerous reports that ambient particulate matter is a key determinant for human health, toxicity data produced based on physicochemical properties of particulate matters is very lack, suggesting lack of scientific evidence for regulation. In this study, we sampled inhalable particulate matters (PM10) in northern Seoul, Korea. PM10 showed atypical- and fiber-type particles with the average size and the surface charge of 1, 598.1 ± 128.7 nm and −27.5 ± 2.8, respectively, and various toxic elements were detected in the water extract. On day 90 after the first pulmonary exposure, total cell number dose-dependently increased in the lungs of both sexes of mice. PM10 induced Th1-dominant immune response with pathological changes in both sexes of mice. Meanwhile, composition of total cells and expression of proteins which functions in cell-to-cell communication showed different trends between sexes. Following, male and female mice were mated to identify effects of PM10 to the next generation. PM10 remained in the lung of dams until day 21 after birth, and the levels of IgA and IgE increased in the blood of dams exposed to the maximum dose compared to control. In addition, the interval between births of fetuses, the number of offspring, the neonatal survival rate (day 4 after birth) and the sex ratio seemed to be affected at the maximum dose, and particularly, all offspring from one dam were stillborn. In addition, expression of HIF-1α protein increased in the lung tissue of dams exposed to PM10, and level of hypoxia-related proteins was notably enhanced in PM10-exposed bronchial epithelial cells compared to control. Taken together, we suggest that inhaled PM10 may induce Th1-shifting immune response in the lung, and that it may affect reproduction (fetus development) by causing lung hypoxia. Additionally, we propose that further study is needed to identify particle-size-dependent effects on development of the next generation.