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Pulmonary hazards of nanoplastic particles: a study using polystyrene in in vitro models of the alveolar and bronchial epithelium
ID
Michelini, Sara
(
Author
),
ID
Mawas, Safaa
(
Author
),
ID
Kurešepi, Ema
(
Author
),
ID
Šimunović, Katarina
(
Author
),
ID
Repar, Neža
(
Author
),
ID
Šetina, Barbara
(
Author
),
ID
Mandić-Mulec, Ines
(
Author
),
ID
Erman, Andreja
(
Author
),
ID
Drobne, Damjana
(
Author
), et al.
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https://jnanobiotechnology.biomedcentral.com/articles/10.1186/s12951-025-03419-6
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Abstract
Background Nanoplastics (NPs) are released into the environment through the degradation of plastic objects, leading to human exposure. Due to their small size, concerns have been raised about the potential hazards to the respiratory tract, as ultrafine and nanoparticles are known to penetrate till the alveolar regions of the lungs, potentially impairing their functions. Thus, in the present study, we used model polystyrene nanoparticles doped with the fluorescent metal europium (PS-Eu) to enhance the understanding of NPs hazard and investigate adverse outcomes associated with exposure in human lungs using alveolar (A549) and bronchial (Calu-3) cell models grown in 2D and 3D submerged conditions or quasi air-liquid interface (ALI) conditions (3D). Results Briefly, after in-dept physicochemical characterization of the particles, we assessed their impact on ROS production, cell viability (AlamarBlue and lactate dehydrogenase assays) and barrier integrity (lucifer yellow assay and TEER measurement), finding no negative effects in either model. However, in alveolar cells, particles increased acidic organelle activity. Transmission electron microscopy and Raman microscopy showed, in both models, a dose- and cell-dependent particle uptake with PS-Eu accumulating in numerous and large endo-lysosomes, which, in transwells-grown A549 cells, often contained also lamellar bodies (LBs), organelles involved in surfactants storage and secretion. After extensively quantifying surfactant proteins (SP) in the pellet and supernatant fractions of treated A549 cells, we observed a significant reduction in several members of this family, including surfactant protein B, which is crucial for lamellar body formation and surface tension regulation in the lungs. In quasi-ALI Calu-3 cultures instead, PS-Eu significantly upregulated interleukin 6 (IL-6) and increased transforming growth factor beta β (TGF-β), zonula occludens 1 (ZO-1), and mucin (MUC) 5B mRNA expressions causing a moderate proinflammatory response. Conclusion Our results show that PS-Eu exposure does not induce acute cytotoxicity in these models, but affects cell-specific functions like surfactant, mucin, and cytokine production. This underscores the limitations of relying solely on standard cytotoxicity tests for particle hazard assessment and highlights the importance of investigating cell function-specific signaling pathways. To support researchers in hazard assessment, we propose specific classes of biomarkers to test in in vitro lung models.
Language:
English
Keywords:
nanoplastic
,
surfactant protein
,
mucin
,
lamellar body
,
A549
,
Calu-3
,
polystyrene
,
alveoli
,
bronchi
,
transwells
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
BF - Biotechnical Faculty
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2025
Number of pages:
34 str.
Numbering:
Vol. 23, art. 388
PID:
20.500.12556/RUL-181759
UDC:
616.2:620.3
ISSN on article:
1477-3155
DOI:
10.1186/s12951-025-03419-6
COBISS.SI-ID:
238925059
Publication date in RUL:
15.04.2026
Views:
414
Downloads:
251
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Record is a part of a journal
Title:
Journal of nanobiotechnology
Shortened title:
J. nanobiotechol.
Publisher:
Springer Nature
ISSN:
1477-3155
COBISS.SI-ID:
2607636
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
nanoplastika
,
polistiren
,
dihala
,
alveole
,
bronhiji
,
celične linije
,
citotoksičnost
Projects
Funder:
EC - European Commission
Funding programme:
Horizon 2020
Project number:
965367
Name:
Plastics fate and effects in the human body
Acronym:
PlasticsFatE
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P4-0116
Name:
Mikrobiologija in biotehnologija živil in okolja
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0207
Name:
Toksini in biomembrane
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P2-0424
Name:
Dizajn novih lastnosti (nano)materialov & aplikacije
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P3-0108
Name:
Celična biologija in molekularna genetika v biomedicini
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J3-2521
Name:
Vnetni proces pri intersticijskem cistitisu in ovrednotenje delovanja agonistov kanabinoidnih receptorjev sečnega mehurja – od celic do pacienta
Funder:
Université Paris Cité
Funding programme:
Ecole Doctorale MTCI
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