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Research on the toxicity of nanoparticles has developed over recent years due to their increasing prevalence in common everyday materials. Various nanoparticles have been reported to promote and induce mucus secretion, which could potentially lead to airway damages and respiratory complications. Lanthanum strontium manganite (LSM) is a nanoparticle widely used in solar oxidized fuel cells (SOFCs) due to its high electrical conductivity, high electrochemical activity for O2 reduction reaction, high thermal stability and compatibility of SOFC electrolytes, and most importantly, its microstructural stability and long-term performance. Very few studies have been conducted on LMS's toxicity, thus its effect on airway cells was investigated in this study. After treating trachea cells with increasing concentrations of LSM ranging up to 500 μg/ml, we found that it has a moderate effect on cell viability, ROS production, cytochrome C, and caspase 3 expression. Despite its minimal impact on stated apoptosis-inducing characteristics, LSM illustrated an inhibiting effect on mucus secretion. We obtained a decreasing trend in mucus secretion with an increased concentration of the LSM treatment. Overall, LSM's advancement in SOFCs necessitated a toxicity study, and although it does not show a significant toxicity to trachea cells, LSM reduces mucus secretion, and can potentially interfere with airway clearance.

Nanotoxicity studies associated with various nanoparticles (NPs) have attracted intense research interest due to the broader applications of nanoparticles in our daily lives. The exposure of nanoparticles can lead to hypersecretion and accumulation of airway mucus which are closely associated with many respiratory diseases. Titanium dioxide (TiO2), one of the PM10 components, is a major NP that is widely utilized in many commercial products. Our previous study established the connection between induced airway mucus secretion and TiO2 NPs. However, the countermeasure to reduce the harmful effects of TiO2 NPs, especially airway mucus secretion, remains unexplored. One of the potential candidates to reduce airway mucus secretion is cerium oxide (CeO2) NPs. It has been reported that CeO2 NPs can protect cells by diminishing ROS and inflammatory responses. Herein, our study shows that CeO2 NPs are able to reduce cytosolic Ca2+ changes and mitochondrial damage caused by TiO2 NPs. Our results provide the evidence that hypersecretion of mucus and apoptosis progression induced by TiO2 NPs can be attenuated by CeO2 NPs. This study highlights the potential capacity of CeO2 NPs as a supplementary material for TiO2 NPs applications in the future.

Engineered nanoparticles (ENPs), products from modern nanotechnologies, can potentially impact the marine environment to pose serious threats to marine ecosystems. However, the cellular responses of marine phytoplankton to ENPs are still not well established. Here, we investigate four different diatom species (Odontella mobiliensis, Skeletonema grethae, Phaeodactylum tricornutum, Thalassiosira pseudonana) and one green algae (Dunaliella tertiolecta) for their extracellular polymeric substances (EPS) release under model ENP treatments: 25 nm titanium dioxide (TiO2), 10-20 nm silicon dioxide (SiO2), and 15-30 nm cerium dioxide (CeO2). We found SiO2 ENPs can significantly stimulate EPS release from these algae (200-800%), while TiO2 ENP exposure induced the lowest release. Furthermore, the increase of intracellular Ca2+ concentration can be triggered by ENPs, suggesting that the EPS release process is mediated through Ca2+ signal pathways. With better understanding of the cellular mechanism mediated ENP-induced EPS release, potential preventative and safety measures can be developed to mitigate negative impact on the marine ecosystem.

Bamboo mosaic virus (Ba MV) is a single-stranded positive-sense RNA virus. One of the plant glutathione S-transferase ( GST) genes, Nb GSTU4, responds as an upregulated gene in Nicotiana benthamiana post Ba MV infection., In order to identify the role of Nb GSTU4 in Ba MV infection, the expression of Nb GSTU4 was knocked down using a virus-induced gene silencing technique or was transiently expressed in N. benthamiana in Ba MV inoculation., The results show a significant decrease in Ba MV RNA accumulation when the expression level of Nb GSTU4 is reduced; whereas the viral RNA accumulation increases when Nb GSTU4 is transiently expressed. Furthermore, this study identified that the involvement of Nb GSTU4 in viral RNA accumulation occurs by its participation in the viral early replication step. The findings show that the Nb GSTU4 protein expressed from Escherichia coli can interact with the 3′ untranslated region ( UTR) of the Ba MV RNA in vitro in the presence of glutathione ( GSH). The addition of GSH in the in vitro replication assay shows an enhancement of minus-strand but not plus-strand RNA synthesis., The results suggest that the plant GST protein plays a role in binding viral RNA and delivering GSH to the replication complex to create a reduced condition for Ba MV minus-strand RNA synthesis. [ABSTRACT FROM AUTHOR]