A comparative analysis of in vitro toxicity of synthetic zeolites on imr-90 human lung fibroblast cells

Seung Hye Yu, Manjesh Kumar, Il Won Kim, Jeffrey D. Rimer, Tae Jung Kim

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5 Scopus citations

Abstract

Broad industrial application of zeolites increases the opportunity of inhalation. However, the potential impact of different type and composition of zeolite on the cytotoxicity is still unknown. Four types of synthetic zeolites with have been prepared for assessing the effect on lung fibroblast: two zeolite L (LTL-R and LTL-D, ZSM-5 (MFI-S), and faujasite (FAU-S). The cytotoxicity of zeolites on human lung fibroblast (IMR-90) was assessed using WST1 cell proliferation assay, mitochondrial function, membrane leakage of lactate dehydrogenase, reduced glutathione levels, and mitochondrial membrane potential were assessed under control. Intracellular changes were examined using transmission electron microscopy (TEM). Toxicity related gene expression were evaluated by PCR array. The result showed a significantly higher toxicity in IMR-90 cells with FAU-S than LTL-R, LTL-D and MFI-S exposure. TEM showed FAU-S, spheroidal zeolite with a low Si/Al ratio, was readily internalized forming numerous phagosomes in IMR-90 cells, while the largest and disc-shaped zeolites showed the lowest toxicity and were located in submembranous phagosomes in IMR-90 cells. Differential expression of TNF related genes was detected using PCR arrays and confirmed using qRT-PCR analysis of selected genes. Collectively, the exposure of different zeolites shows different toxicity on IMR-90 cells.

Original languageEnglish
Article number3194
JournalMolecules
Volume26
Issue number11
DOIs
StatePublished - 1 Jun 2021

Bibliographical note

Funding Information:
Acknowledgments: This study was supported by Institute of Clinical Medicine Research at Yeouido St. Mary’s Hospital.

Funding Information:
Funding: This work was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (2017R1E1A1A01078335), and the Radiation Safety Materials and Medical Technology R&D program through the National Research Foundation of Korea funded by the Ministry of Science and ICT (NRF-2019M2C8A2058418). JDR acknowledges financial support from the Welch Foundation (Award E-1794).

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Keywords

  • Cytotoxicity
  • Fibroblast
  • Glutathione
  • IMR-90
  • Lung
  • Zeolite

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