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Formation of lamellar body-like structure may be an initiator of didecyldimethylammonium chloride-induced toxic response

Authors
Park, Eun-JungSeong, EunsolKang, Min-SungLee, Gwang-HeeKim, Dong-WanHan, Ji-SeokLim, Hyun-JiLee, Seung HyeunHan, Hyoung-Yun
Issue Date
1-10월-2020
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Didecyldimethylammonium chloride; Disinfectants; Quaternary ammonium compounds; Lamella body; Matrix metalloproteinase-1; Idiopathic pulmonary fibrosis
Citation
TOXICOLOGY AND APPLIED PHARMACOLOGY, v.404
Indexed
SCIE
SCOPUS
Journal Title
TOXICOLOGY AND APPLIED PHARMACOLOGY
Volume
404
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/52501
DOI
10.1016/j.taap.2020.115182
ISSN
0041-008X
Abstract
Due to the pandemic of coronavirus disease 2019, the use of disinfectants is rapidly increasing worldwide. Didecyldimethylammonium chloride (DDAC) is an EPA-registered disinfectant, it was also a component in humidifier disinfectants that had caused idiopathic pulmonary diseases in Korea. In this study, we identified the possible pulmonary toxic response and mechanism using human bronchial epithelial (BEAS-2B) cells and mice. First, cell viability decreased sharply at a 4 mu g/mL of concentration. The volume of intracellular organelles and the ROS level reduced, leading to the formation of apoptotic bodies and an increase of the LDH release. Secretion of pro-inflammatory cytokines (IL-1 beta, IL-6, and TNF-alpha) and matrix metalloproteinase-1 also significantly increased. More importantly, lamellar body-like structures were formed in both the cells and mice exposed to DDAC, and the expression of both the indicator proteins for lamellar body (ABCA3 and Rab11a) and surfactant proteins (A, B, and D) was clearly enhanced. In addition, chronic fibrotic pulmonary lesions were notably observed in mice instilled twice (weekly) with DDAC (500 mu g), ultimately resulting in death. Taken together, we suggest that disruption of pulmonary surfactant homeostasis may contribute to DDAC-induced cell death and subsequent pathophysiology and that the formation of lamellar body-like structures may play a role as the trigger. In addition, we propose that the cause of sudden death of mice exposed to DDAC should be clearly elucidated for the safe application of DDAC.
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