scholarly journals The Toxic Effect of Water-Soluble Particulate Pollutants from Biomass Burning on Alveolar Lung Cells

Atmosphere ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 1023
Author(s):  
Yuri Lima de Albuquerque ◽  
Emmanuelle Berger ◽  
Chunlin Li ◽  
Michal Pardo ◽  
Christian George ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Biomass Burning ◽  
Optical Thickness ◽  
Water Soluble ◽  
Lung Cells ◽  
Cell Analysis ◽  
Wood Combustion ◽  
Wood Burning ◽  
Particulate Pollutants ◽  
Behavioral Parameters

In 2018, 3.8 million premature deaths were attributed to exposure to biomass burning nanoparticles from wood combustion. The objective of this study was to investigate and compare the toxic effect of wood-combustion-related biomass burning nanoparticles from three different combustion stages (i.e., flaming, smoldering, and pyrolysis) on alveolar lung cells, by studying cell proliferation, and structural and behavioral parameters. A549 lung epithelial cells were treated with 31, 62, 125, 250, and 500 µg/mL of water-soluble particulate pollutants from wood burning, and measured by means of real-time cell analysis, cell imaging, and phase imaging microscopy. At low concentrations (31 and 62 µg/mL), all three types of wood burning samples exhibited no toxicity. At 125 µg/mL, they caused decreased cell proliferation compared to the control. Exposure to higher concentrations (250 and 500 µg/mL) killed the cells. Cell physical parameters (area, optical volume, eccentricity, perimeter, and optical thickness) and behavioral parameters (migration, motility, and motility speed) did not change in response to exposure to wood burning materials up to a concentration of 125 µg/mL. Exposure to higher concentrations (250 and 500 µg/mL) changed cell perimeter, optical thickness for smoldering and flaming particles, and led to decreased migration, motility, and motility speed of cells. In conclusion, all three of the combustion water-soluble organic pollutants were identified as equally toxic by real-time cell analysis (RTCA) results. The parameters describing cell structure suggest that pyrolysis particles were slightly less toxic than others.

scholarly journals S-Allylcysteine as an Inhibitor of Benzo(a)pyrene-Induced Precancerous Carcinogenesis in Human Lung Cells via Inhibiting Activation of Nuclear Factor-Kappa B

2019 ◽  
Vol 14 (12) ◽  
pp. 1934578X1989691
Author(s):  
Kaiming Wang ◽  
Qiuchen Qi ◽  
Fang Zhang ◽  
Yongchun Zhang ◽  
Min Yang ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Nuclear Factor Kappa B ◽  
Human Lung ◽  
Water Soluble ◽  
Human Lung Cancer ◽  
Lung Cells ◽  
Organosulfur Compounds ◽  
Nuclear Factor ◽  
Nuclear Factor Kappa ◽  
Human Lung Cells

Oil-soluble organosulfur compounds in garlic are known for the anticancer effect. However, there are limited experimental studies to describe the effect of S-allylcysteine (SAC), a main water-soluble derivative of garlic, in carcinogenesis. This study investigates the prevention function of SAC on carcinogen benzo(a)pyrene (B(a)P)-induced precancerous activity in human lung cells (A549). A549 cells were either pretreated (PreTM) or concurrently treated (CoTM) with 1 μM B(a)P and either 10 or 50 μM SAC. The 50 μM CoTM group inhibited B(a)P-induced cell proliferation by approximately 100%. The 50 μM SAC CoTM and PreTM inhibited the B(a)P-induced G2/M phase shift by 119% and 100%, respectively. Furthermore, the SAC PreTM exhibited the potential to reduce the generation of reactive oxygen species (ROS) in cells relative to the B(a)P group by approximately 100%. The CoTM and PreTM elevated superoxide dismutase (SOD) by at least 70% compared with B(a)P group. In this study, we demonstrated that the mechanisms involved in the inhibitory role of SAC in B(a)P-induced carcinogenesis, including suppression of cell proliferation and DNA damage, cell cycle regulation, attenuation of ROS formation, increase of SOD activity, and inhibition of nuclear factor-kappa B (NF-κB) activity, which indicated that SAC is potentially a novel therapeutic candidate for the prevention and treatment of B(a)P-induced human lung cancer.

Synthesis of mussel-inspired polydopamine-gallium nanoparticles for biomedical applications

Nanomedicine ◽  
2021 ◽  
Author(s):  
Jean Valdir Uchôa Teixeira ◽  
Fátima Raquel Azevedo Maia ◽  
Mariana Carvalho ◽  
Rui Reis ◽  
Joaquim Miguel Oliveira ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Biomedical Applications ◽  
Adipose Derived Stem Cells ◽  
Cell Analysis ◽  
Shell Formation ◽  
X Ray ◽  
Alkali Medium ◽  
Reproducible Method ◽  
Gallium Nanoparticles

Aim: To established a simple, controlled and reproducible method to synthesize gallium (Ga)-coated polydopamine (PDA) nanoparticles (NPs). Materials & methods: PDA NPs were synthesized in alkali medium with posterior Ga shell formation due to ion chelation on the NP surface. Results: The obtained results with energy-dispersive x-ray spectroscopy confirmed the incorporation of Ga on the PDA NP surface. The cytotoxicity of Ga-coated PDA NPs was evaluated in vitro at different concentrations in contact with human adipose-derived stem cells. Further cell analysis also demonstrated the benefit of Ga-coated PDA NPs, which increased the cell proliferation rate compared with noncoated PDA NPs. Conclusion: This study indicated that Ga could work as an appropriate shell for PDA NPs, inducing cell proliferation at the analyzed concentrations.

scholarly journals Forecasting carbon monoxide on a global scale for the ATom-1 aircraft mission: insights from airborne and satellite observations and modeling

2018 ◽  
Vol 18 (15) ◽  
pp. 10955-10971 ◽  
Author(s):  
Sarah A. Strode ◽  
Junhua Liu ◽  
Leslie Lait ◽  
Róisín Commane ◽  
Bruce Daube ◽  
...  
Keyword(s):  
Biomass Burning ◽  
Optical Thickness ◽  
Chemical Reactivity ◽  
Model Performance ◽  
Global Scale ◽  
Satellite Observations ◽  
Aerosol Optical Thickness ◽  
Boreal Summer ◽  
Large Contribution ◽  
Moderate Resolution Imaging Spectroradiometer

Abstract. The first phase of the Atmospheric Tomography Mission (ATom-1) took place in July–August 2016 and included flights above the remote Pacific and Atlantic oceans. Sampling of atmospheric constituents during these flights is designed to provide new insights into the chemical reactivity and processes of the remote atmosphere and how these processes are affected by anthropogenic emissions. Model simulations provide a valuable tool for interpreting these measurements and understanding the origin of the observed trace gases and aerosols, so it is important to quantify model performance. Goddard Earth Observing System Model version 5 (GEOS-5) forecasts and analyses show considerable skill in predicting and simulating the CO distribution and the timing of CO enhancements observed during the ATom-1 aircraft mission. We use GEOS-5's tagged tracers for CO to assess the contribution of different emission sources to the regions sampled by ATom-1 to elucidate the dominant anthropogenic influences on different parts of the remote atmosphere. We find a dominant contribution from non-biomass-burning sources along the ATom transects except over the tropical Atlantic, where African biomass burning makes a large contribution to the CO concentration. One of the goals of ATom is to provide a chemical climatology over the oceans, so it is important to consider whether August 2016 was representative of typical boreal summer conditions. Using satellite observations of 700 hPa and column CO from the Measurement of Pollution in the Troposphere (MOPITT) instrument, 215 hPa CO from the Microwave Limb Sounder (MLS), and aerosol optical thickness from the Moderate Resolution Imaging Spectroradiometer (MODIS), we find that CO concentrations and aerosol optical thickness in August 2016 were within the observed range of the satellite observations but below the decadal median for many of the regions sampled. This suggests that the ATom-1 measurements may represent relatively clean but not exceptional conditions for lower-tropospheric CO.

scholarly journals HIV-1 Nef promotes cell proliferation and microRNA dysregulation in lung cells

Cell Cycle ◽  
2019 ◽  
Vol 18 (2) ◽  
pp. 130-142 ◽  
Author(s):  
Maryline Santerre ◽  
Wissam Chatila ◽  
Ying Wang ◽  
Ruma Mukerjee ◽  
Bassel E Sawaya
Keyword(s):  
Cell Proliferation ◽  
Lung Cells ◽  
Microrna Dysregulation ◽  
Hiv 1

scholarly journals Quantifying primary and secondary humic-like substances in urban aerosol based on emission source characterization and a source-oriented air quality model

2018 ◽  
Author(s):  
Xinghua Li ◽  
Junzan Han ◽  
Philip K. Hopke ◽  
Jingnan Hu ◽  
Qi Shu ◽  
...  
Keyword(s):  
Organic Carbon ◽  
Biomass Burning ◽  
Coal Combustion ◽  
Power Plants ◽  
Water Soluble ◽  
Aerosol Formation ◽  
Source Characterization ◽  
Air Quality Model ◽  
Coal Burning ◽  
Residential Coal

Abstract. Humic-like substances (HULIS) are a mixture of high molecular weight, water-soluble organic compounds that are widely distributed in atmospheric aerosol. Their sources are rarely studied quantitatively. Biomass burning is generally accepted as a major primary source of ambient humic-like substances (HULIS) with additional secondary material formed in the atmosphere. However, the present study provides direct evidence that residential coal burning is also a significant source of ambient HULIS, especially in the heating season in northern China based on source measurements, ambient sampling and analysis, and apportionment with source-oriented CMAQ modeling. Emissions tests show that residential coal combustion produces 5 to 24 % of the emitted organic carbon (OC) as HULIS carbon (HULISc). Estimation of primary emissions of HULIS in Beijing indicated that residential biofuel and coal burning contribute about 70 % and 25 % of annual primary HULIS, respectively. Vehicle exhaust, industry, and power plants contributions are negligible. Average concentration of ambient HULIS was 7.5 μg/m3 in atmospheric PM2.5 in urban Beijing and HULIS exhibited obvious seasonal variations with the highest concentrations in winter. HULISc account for 7.2 % of PM2.5 mass, 24.5 % of OC, and 59.5 % of water-soluble organic carbon, respectively. HULIS are found to correlate well with K+, Cl−, sulfate, and secondary organic aerosol suggesting its sources include biomass burning, coal combustion and secondary aerosol formation. Source apportionment based on CMAQ modeling shows residential biofuel and coal burning, secondary formation are important annual sources of ambient HULIS, contributing 57.5 %, 12.3 %, and 25.8 %, respectively.

scholarly journals Characterization of gas-phase organics using proton transfer reaction time-of-flight mass spectrometry: fresh and aged residential wood combustion emissions

2016 ◽  
Author(s):  
Emily A. Bruns ◽  
Jay G. Slowik ◽  
Imad El Haddad ◽  
Dogushan Kilic ◽  
Felix Klein ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Reaction Time ◽  
Biomass Burning ◽  
Transfer Reaction ◽  
Proton Transfer Reaction ◽  
Wood Combustion ◽  
Flight Mass Spectrometry ◽  
Combustion Emissions ◽  
Organic Gases

Abstract. Organic gases emitted during the flaming phase of residential wood combustion are characterized individually and by functionality using proton transfer reaction time-of-flight mass spectrometry. The evolution of the organic gases is monitored during photochemical aging. Primary gaseous emissions are dominated by oxygenated species (e.g., acetic acid, acetaldehyde, phenol and methanol), many of which have deleterious health effects and play an important role in atmospheric processes such as secondary organic aerosol formation and ozone production. Residential wood combustion emissions differ considerably from open biomass burning in both absolute magnitude and relative composition. Ratios of acetonitrile, a potential biomass burning marker, to CO are considerably lower (~ 0.09 pptv ppbv−1) than those observed in air masses influenced by open burning (~ 1–2 pptv ppbv−1), which may make differentiation from background levels difficult, even in regions heavily impacted by residential wood burning. Considerable formic acid forms during aging (~ 200–600 mg kg−1 at an OH exposure of (4.5–5.5) × 107 molec  cm−3 h), indicating residential wood combustion can be an important local source for this acid, the quantities of which are currently underestimated in models. Phthalic anhydride, a naphthalene oxidation product, is also formed in considerable quantities with aging (~ 55–75 mg kg−1 at an OH exposure of (4.5–5.5) × 107 molec  cm−3 h). Although total NMOG emissions vary by up to a factor of ~ 9 between burns, SOA formation potential does not scale with total NMOG emissions and is similar in all experiments. This study is the first thorough characterization of both primary and aged organic gases from residential wood combustion and provides a benchmark for comparison of emissions generated under different burn parameters.

scholarly journals Remote sensing of aerosols by synergy of caliop and modis

2018 ◽  
Vol 176 ◽  
pp. 08012
Author(s):  
Rei Kudo ◽  
Tomoaki Nishizawa ◽  
Akiko Higurashi ◽  
Eiji Oikawa
Keyword(s):  
Remote Sensing ◽  
Biomass Burning ◽  
Sea Salt ◽  
Water Soluble ◽  
Dust Particles ◽  
Vertical Profiles ◽  
Dust Event ◽  
Carbonaceous Particles ◽  
The Individual ◽  
Better Than

For the monitoring of the global 3-D distribution of aerosol components, we developed the method to retrieve the vertical profiles of water-soluble, light absorbing carbonaceous, dust, and sea salt particles by the synergy of CALIOP and MODIS data. The aerosol product from the synergistic method is expected to be better than the individual products of CALIOP and MODIS. We applied the method to the biomass-burning event in Africa and the dust event in West Asia. The reasonable results were obtained; the much amount of the water-soluble and light absorbing carbonaceous particles were estimated in the biomass-burning event, and the dust particles were estimated in the dust event.

Novel powerful water-soluble lipid immunoadjuvants inducing mouse dendritic cell maturation and B cell proliferation using TLR2 pathway

2010 ◽  
Vol 20 (6) ◽  
pp. 1869-1872 ◽  
Author(s):  
Maria Vittoria Spanedda ◽  
Béatrice Heurtault ◽  
Steffen Weidner ◽  
Corinne Baehr ◽  
Emmanuelle Boeglin ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Dendritic Cell ◽  
B Cell ◽  
Dendritic Cell Maturation ◽  
Water Soluble ◽  
Cell Maturation ◽  
Mouse Dendritic Cell

scholarly journals Sources and formation of carbonaceous aerosols in Xi'an, China: primary emissions and secondary formation constrained by radiocarbon

2020 ◽  
Author(s):  
Haiyan Ni ◽  
Ru-Jin Huang ◽  
Ulrike Dusek
Keyword(s):  
Biomass Burning ◽  
Coal Combustion ◽  
Vehicle Emissions ◽  
Fossil Fuel ◽  
Fuel Combustion ◽  
Warm Period ◽  
Water Soluble ◽  
Formation Mechanisms ◽  
Carbonaceous Aerosols ◽  
Fossil Fuel Combustion

<p>To investigate the sources and formation mechanisms of carbonaceous aerosols, a major contributor to severe particulate air pollution, radiocarbon (<span><sup>14</sup>C</span>) measurements were conducted on aerosols sampled from November 2015 to November 2016 in Xi'an, China. Based on the <span><sup>14</sup>C</span> content in elemental carbon (EC), organic carbon (OC) and water-insoluble OC (WIOC), contributions of major sources to carbonaceous aerosols are estimated over a whole seasonal cycle: primary and secondary fossil sources, primary biomass burning, and other non-fossil carbon formed mainly from secondary processes. Primary fossil sources of EC were further sub-divided into coal and liquid fossil fuel combustion by complementing <span><sup>14</sup>C</span> data with stable carbon isotopic signatures.</p><p>The dominant EC source was liquid fossil fuel combustion (i.e., vehicle emissions), accounting for 64 % (median; 45 %–74 %, interquartile range) of EC in autumn, 60 % (41 %–72 %) in summer, 53 % (33 %–69 %) in spring and 46 % (29 %–59 %) in winter. An increased contribution from biomass burning to EC was observed in winter (<span>∼28</span> %) compared to other seasons (warm period; <span>∼15</span> %). In winter, coal combustion (<span>∼25</span> %) and biomass burning equally contributed to EC, whereas in the warm period, coal combustion accounted for a larger fraction of EC than biomass burning. The relative contribution of fossil sources to OC was consistently lower than that to EC, with an annual average of <span>47±4</span> %. Non-fossil OC of secondary origin was an important contributor to total OC (<span>35±4</span> %) and accounted for more than half of non-fossil OC (<span>67±6</span> %) throughout the year. Secondary fossil OC (SOC<span><sub>fossil</sub></span>) concentrations were higher than primary fossil OC (POC<span><sub>fossil</sub></span>) concentrations in winter but lower than POC<span><sub>fossil</sub></span> in the warm period.</p><p>Fossil WIOC and water-soluble OC (WSOC) have been widely used as proxies for POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span>, respectively. This assumption was evaluated by (1) comparing their mass concentrations with POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span> and (2) comparing ratios of fossil WIOC to fossil EC to typical primary OC-to-EC ratios from fossil sources including both coal combustion and vehicle emissions. The results suggest that fossil WIOC and fossil WSOC are probably a better approximation for primary and secondary fossil OC, respectively, than POC<span><sub>fossil</sub></span> and SOC<span><sub>fossil</sub></span> estimated using the EC tracer method.</p>

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