Platform to study intracellular polystyrene nanoplastic pollution and clinical outcomes.

TitlePlatform to study intracellular polystyrene nanoplastic pollution and clinical outcomes.
Publication TypeJournal Article
Year of Publication2020
AuthorsBojic, S, Falco, MM, Stojkovic, P, Ljujic, B, Jankovic, MGazdic, Armstrong, L, Markovic, N, Dopazo, J, Lako, M, Bauer, R, Stojkovic, M
JournalStem Cells
Volume38
Issue10
Pagination1321-1325
Date Published2020 Oct 01
ISSN1549-4918
Abstract

Increased pollution by plastics has become a serious global environmental problem, but the concerns for human health have been raised after reported presence of microplastics (MPs) and nanoplastics (NPs) in food and beverages. Unfortunately, few studies have investigate the potentially harmful effects of MPs/NPs on early human development and human health. Therefore, we used a new platform to study possible effects of polystyrene NPs (PSNPs) on the transcription profile of preimplantation human embryos and human induced pluripotent stem cells (hiPSCs). Two pluripotency genes, LEFTY1 and LEFTY2, which encode secreted ligands of the transforming growth factor-beta, were downregulated, while CA4 and OCLM, which are related to eye development, were upregulated in both samples. The gene set enrichment analysis showed that the development of atrioventricular heart valves and the dysfunction of cellular components, including extracellular matrix, were significantly affected after exposure of hiPSCs to PSNPs. Finally, using the HiPathia method, which uncovers disease mechanisms and predicts clinical outcomes, we determined the APOC3 circuit, which is responsible for increased risk for ischemic cardiovascular disease. These results clearly demonstrate that better understanding of NPs bioactivities and its implications for human health is of extreme importance. Thus, the presented platform opens further aspects to study interactions between different environmental and intracellular pollutions with the aim to decipher the mechanism and origin of human diseases.

DOI10.1002/stem.3244
Alternate JournalStem Cells
PubMed ID32614127
Grant ListON175103 / / Serbian Ministry of Education, Science and Technology /
/ / European Regional Development Funds /
SAF2017-88908-R / / Spanish Ministry of Economy and Competitiveness /
EP/S001433/1 / / Engineering and Physical Sciences Research Council of the United Kingdom /
614629 / / ERC consolidator /