Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs

Consumers and manufacturers are exposed to nanosized zinc oxide (nZnO) and silver particles (nAg) via airways, but their biological effects are still not fully elucidated. To understand the immune effects, we exposed mice to 2, 10, or 50 μg of nZnO or nAg by oropharyngeal aspiration and analyzed the...

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Main Authors: Lan Zhao, Shuyuan Wang, Marit Ilves, Sanna Lehtonen, Leena Saikko, Hani El-Nezami, Harri Alenius, Piia Karisola
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/6/5183
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author Lan Zhao
Shuyuan Wang
Marit Ilves
Sanna Lehtonen
Leena Saikko
Hani El-Nezami
Harri Alenius
Piia Karisola
author_facet Lan Zhao
Shuyuan Wang
Marit Ilves
Sanna Lehtonen
Leena Saikko
Hani El-Nezami
Harri Alenius
Piia Karisola
author_sort Lan Zhao
collection DOAJ
description Consumers and manufacturers are exposed to nanosized zinc oxide (nZnO) and silver particles (nAg) via airways, but their biological effects are still not fully elucidated. To understand the immune effects, we exposed mice to 2, 10, or 50 μg of nZnO or nAg by oropharyngeal aspiration and analyzed the global gene expression profiles and immunopathological changes in the lungs after 1, 7, or 28 days. Our results show that the kinetics of responses varied in the lungs. Exposure to nZnO resulted in the highest accumulation of F4/80- and CD3-positive cells, and the largest number of differentially expressed genes (DEGs) were identified after day 1, while exposure to nAg caused peak responses at day 7. Additionally, nZnO mainly activated the innate immune responses leading to acute inflammation, whereas the nAg activated both innate and adaptive immune pathways, with long-lasting effects. This kinetic-profiling study provides an important data source to understand the cellular and molecular processes underlying nZnO- and nAg-induced transcriptomic changes, which lead to the characterization of the corresponding biological and toxicological effects of nZnO and nAg in the lungs. These findings could improve science-based hazard and risk assessment and the development of safe applications of engineered nanomaterials (ENMs), e.g., in biomedical applications.
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spelling doaj.art-306b81a74a5e48ebb24f5891be21e0cc2023-11-17T11:30:16ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-03-01246518310.3390/ijms24065183Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse LungsLan Zhao0Shuyuan Wang1Marit Ilves2Sanna Lehtonen3Leena Saikko4Hani El-Nezami5Harri Alenius6Piia Karisola7Human Microbiome Research (HUMI), Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandHuman Microbiome Research (HUMI), Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandHuman Microbiome Research (HUMI), Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandDepartment of Pathology, Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandDepartment of Pathology, Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandSchool of Biological Sciences, University of Hong Kong, Hong Kong, ChinaHuman Microbiome Research (HUMI), Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandHuman Microbiome Research (HUMI), Medical Faculty, University of Helsinki, 00014 Helsinki, FinlandConsumers and manufacturers are exposed to nanosized zinc oxide (nZnO) and silver particles (nAg) via airways, but their biological effects are still not fully elucidated. To understand the immune effects, we exposed mice to 2, 10, or 50 μg of nZnO or nAg by oropharyngeal aspiration and analyzed the global gene expression profiles and immunopathological changes in the lungs after 1, 7, or 28 days. Our results show that the kinetics of responses varied in the lungs. Exposure to nZnO resulted in the highest accumulation of F4/80- and CD3-positive cells, and the largest number of differentially expressed genes (DEGs) were identified after day 1, while exposure to nAg caused peak responses at day 7. Additionally, nZnO mainly activated the innate immune responses leading to acute inflammation, whereas the nAg activated both innate and adaptive immune pathways, with long-lasting effects. This kinetic-profiling study provides an important data source to understand the cellular and molecular processes underlying nZnO- and nAg-induced transcriptomic changes, which lead to the characterization of the corresponding biological and toxicological effects of nZnO and nAg in the lungs. These findings could improve science-based hazard and risk assessment and the development of safe applications of engineered nanomaterials (ENMs), e.g., in biomedical applications.https://www.mdpi.com/1422-0067/24/6/5183animal modelimmune effectslungsilver nanoparticlestranscriptomicszinc oxide nanoparticles
spellingShingle Lan Zhao
Shuyuan Wang
Marit Ilves
Sanna Lehtonen
Leena Saikko
Hani El-Nezami
Harri Alenius
Piia Karisola
Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
International Journal of Molecular Sciences
animal model
immune effects
lung
silver nanoparticles
transcriptomics
zinc oxide nanoparticles
title Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
title_full Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
title_fullStr Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
title_full_unstemmed Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
title_short Transcriptomic Profiling the Effects of Airway Exposure of Zinc Oxide and Silver Nanoparticles in Mouse Lungs
title_sort transcriptomic profiling the effects of airway exposure of zinc oxide and silver nanoparticles in mouse lungs
topic animal model
immune effects
lung
silver nanoparticles
transcriptomics
zinc oxide nanoparticles
url https://www.mdpi.com/1422-0067/24/6/5183
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