Detection of intracellular lamellar bodies as a screening marker for fibrotic lesions

Toxicol Appl Pharmacol. 2021 May 1:418:115501. doi: 10.1016/j.taap.2021.115501. Epub 2021 Mar 23.

Abstract

With the rapid increase in application of disinfectants worldwide as a method to block the spread of coronavirus, many new products are being introduced into the market without thorough verification of their impacts on human health and the environment. In the present study, we aimed to propose a screening marker for materials that can induce fibrotic lung disease using disinfectants, which had been demonstrated as causative materials of chronic inflammation and interstitial fibrosis. We first calculated the corresponding LC50 level based on results from cell viability test and exposed the LC50 level of disinfectants to human bronchial epithelial cells for 24 h. Formation of lamellar body-like structures, cleavage of the nuclear matrix, structural damage of mitochondria were found in the cytosol of the treated cells. We also dosed disinfectants by pharyngeal aspiration to mice to determine the LD0 level. The mice were sacrificed on Day 14 after a single dosing, and lamellar body-like structures were observed in the lung tissue of mice. Herein, we hypothesize that DNA damage and metabolic disturbance may play central roles in disinfectant-induced adverse health effects. Additionally, we propose that formation of lamellar bodies can be a screening marker for interstitial fibrosis.

Keywords: Disinfectants; Interstitial fibrosis; Lamellar bodies; Mitochondria; The nuclear matrix cleavage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Disinfectants / toxicity*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology*
  • Female
  • Humans
  • Intracellular Fluid / drug effects*
  • Intracellular Fluid / metabolism
  • Lung Diseases, Interstitial / chemically induced*
  • Lung Diseases, Interstitial / metabolism
  • Lung Diseases, Interstitial / pathology*
  • Mice
  • Mice, Inbred ICR
  • Pulmonary Fibrosis / chemically induced
  • Pulmonary Fibrosis / metabolism
  • Pulmonary Fibrosis / pathology

Substances

  • Biomarkers
  • Disinfectants