Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells

We investigated roles of Hippo signaling pathway components in alveolar type II cells (AECII) after zinc oxide nanoparticle (ZnONP) exposure. ZnONPs physicochemistry was characterized using field emission-scanning electron microscopy (FE-SEM) and energy-dispersive X-ray (EDX) microanalysis. ZnONP de...

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Main Authors: Laiman, Vincent, Heriyanto, Didik Setyo, Lee, Yueh-Lun, Lai, Ching-Huang, Pan, Chih-Hong, Chen, Wei-Liang, Wang, Chung-Ching, Chuang, Kai-Jen, Chang, Jer-Hwa, Chuang, Hsiao-Chi
Format: Article
Language:English
Published: Multidisciplinary Digital Publishing Institute 2022
Subjects:
Online Access:https://repository.ugm.ac.id/283030/1/211.pdf
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author Laiman, Vincent
Heriyanto, Didik Setyo
Lee, Yueh-Lun
Lai, Ching-Huang
Pan, Chih-Hong
Chen, Wei-Liang
Wang, Chung-Ching
Chuang, Kai-Jen
Chang, Jer-Hwa
Chuang, Hsiao-Chi
author_facet Laiman, Vincent
Heriyanto, Didik Setyo
Lee, Yueh-Lun
Lai, Ching-Huang
Pan, Chih-Hong
Chen, Wei-Liang
Wang, Chung-Ching
Chuang, Kai-Jen
Chang, Jer-Hwa
Chuang, Hsiao-Chi
author_sort Laiman, Vincent
collection UGM
description We investigated roles of Hippo signaling pathway components in alveolar type II cells (AECII) after zinc oxide nanoparticle (ZnONP) exposure. ZnONPs physicochemistry was characterized using field emission-scanning electron microscopy (FE-SEM) and energy-dispersive X-ray (EDX) microanalysis. ZnONP deposition in human respiratory tract was estimated using multiple-path particle dosimetry (MPPD) model. MLE-12 AECII were cultured and exposed to 0, 1, and 5 μg/mL of ZnONPs for 24 h. Western blots were used to investigate signaling pathways associated with Yes-associated protein (YAP)/transcriptional co-activator with PDZ-binding motif (TAZ), cell adherens junctions, differentiation, and senescence. ZnONPs morphology was irregular, with Zn and O identified. Approximately 72% of inhaled ZnONPs were deposited in lungs, with 26% being deposited in alveolar regions. ZnONP exposure increased nuclear YAP expression and decreased cytoplasmic YAP expression by AECII. Adherens junction proteins, E-cadherin, α-catenin, and β-catenin, on AECII decreased after ZnONP exposure. ZnONP exposure of AECII increased alveolar type I (AECI) transition protein, LGALS3, and the AECI protein, T1α, while decreasing AECII SPC expression. ZnONP exposure induced Sirt1 and p53 senescence proteins by AECII. Our findings showed that inhalable ZnONPs can deposit in alveoli, which promotes YAP nuclear localization in AECII, resulting in decrease tight junctions, cell differentiation, and cell senescence.
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spelling oai:generic.eprints.org:2830302023-11-17T08:24:10Z https://repository.ugm.ac.id/283030/ Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells Laiman, Vincent Heriyanto, Didik Setyo Lee, Yueh-Lun Lai, Ching-Huang Pan, Chih-Hong Chen, Wei-Liang Wang, Chung-Ching Chuang, Kai-Jen Chang, Jer-Hwa Chuang, Hsiao-Chi Cell Physiology We investigated roles of Hippo signaling pathway components in alveolar type II cells (AECII) after zinc oxide nanoparticle (ZnONP) exposure. ZnONPs physicochemistry was characterized using field emission-scanning electron microscopy (FE-SEM) and energy-dispersive X-ray (EDX) microanalysis. ZnONP deposition in human respiratory tract was estimated using multiple-path particle dosimetry (MPPD) model. MLE-12 AECII were cultured and exposed to 0, 1, and 5 μg/mL of ZnONPs for 24 h. Western blots were used to investigate signaling pathways associated with Yes-associated protein (YAP)/transcriptional co-activator with PDZ-binding motif (TAZ), cell adherens junctions, differentiation, and senescence. ZnONPs morphology was irregular, with Zn and O identified. Approximately 72% of inhaled ZnONPs were deposited in lungs, with 26% being deposited in alveolar regions. ZnONP exposure increased nuclear YAP expression and decreased cytoplasmic YAP expression by AECII. Adherens junction proteins, E-cadherin, α-catenin, and β-catenin, on AECII decreased after ZnONP exposure. ZnONP exposure of AECII increased alveolar type I (AECI) transition protein, LGALS3, and the AECI protein, T1α, while decreasing AECII SPC expression. ZnONP exposure induced Sirt1 and p53 senescence proteins by AECII. Our findings showed that inhalable ZnONPs can deposit in alveoli, which promotes YAP nuclear localization in AECII, resulting in decrease tight junctions, cell differentiation, and cell senescence. Multidisciplinary Digital Publishing Institute 2022 Article PeerReviewed application/pdf en https://repository.ugm.ac.id/283030/1/211.pdf Laiman, Vincent and Heriyanto, Didik Setyo and Lee, Yueh-Lun and Lai, Ching-Huang and Pan, Chih-Hong and Chen, Wei-Liang and Wang, Chung-Ching and Chuang, Kai-Jen and Chang, Jer-Hwa and Chuang, Hsiao-Chi (2022) Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells. Atmosphere, 13 (2). p. 334. ISSN 2073-4433 https://www.mdpi.com/2073-4433/13/2/334 10.3390/atmos13020334
spellingShingle Cell Physiology
Laiman, Vincent
Heriyanto, Didik Setyo
Lee, Yueh-Lun
Lai, Ching-Huang
Pan, Chih-Hong
Chen, Wei-Liang
Wang, Chung-Ching
Chuang, Kai-Jen
Chang, Jer-Hwa
Chuang, Hsiao-Chi
Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title_full Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title_fullStr Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title_full_unstemmed Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title_short Zinc Oxide Nanoparticles Promote YAP/TAZ Nuclear Localization in Alveolar Epithelial Type II Cells
title_sort zinc oxide nanoparticles promote yap taz nuclear localization in alveolar epithelial type ii cells
topic Cell Physiology
url https://repository.ugm.ac.id/283030/1/211.pdf
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