Evidence for cytotoxicity and mitochondrial dysfunction in human lung cells exposed to biomass burning aerosol constituents: Levoglucosan and 4-nitrocatechol

Biomass burning (BB) emissions are one of the largest sources of carbonaceous aerosol, posing a significant risk as an airway irritant. Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β...

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Veröffentlicht in:Environmental pollution (1987) 2024-12, Vol.363 (Pt 2), p.125173, Article 125173
Hauptverfasser: Khan, Faria, Kwapiszewska, Karina, Romero, Alicia M., Rudzinski, Krzysztof, Gil-Casanova, Domingo, Surratt, Jason D., Szmigielski, Rafal
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container_end_page
container_issue Pt 2
container_start_page 125173
container_title Environmental pollution (1987)
container_volume 363
creator Khan, Faria
Kwapiszewska, Karina
Romero, Alicia M.
Rudzinski, Krzysztof
Gil-Casanova, Domingo
Surratt, Jason D.
Szmigielski, Rafal
description Biomass burning (BB) emissions are one of the largest sources of carbonaceous aerosol, posing a significant risk as an airway irritant. Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β-D-glucopyranose). Atmospheric chemical aging of BB-derived aerosol (BBA) in the presence of nitrogen oxides (NOx) can yield nitro-aromatic compounds, including 4-nitrocatechol (4NC). There is building evidence that NOx-mediated chemical aging of BBA poses a more serious exposure effect than primary pyrolysis emissions. This study provides a comparative toxicological assessment following the exposure to important BBA marker compounds in human lung cells (i.e., A549 and BEAS-2B) to determine whether aromatic 4NC is more toxic than BBA-bound anhydrous carbohydrate (i.e., LG). We determined inhibitory concentration-50 (IC50) and examined reactive oxygen species (ROS) changes, mitochondrial dysfunction, and apoptosis induction in the two cell lines following exposure to LG and 4NC in a dose-response manner. In the BEAS-2B cells, estimated IC50 values for 4NC were 33 and 8.8 μg mL−1, and for LG were 2546 and ∼3 × 107 μg mL−1 at 24 h and 48 h of exposure, respectively. A549 cells exhibited a much higher IC50 value than BEAS-2B cells. LG exposures resulted in mitochondrial stress with viability inhibition, but cells recovered with increasing exposure time. 4NC exposures at 200 μg mL−1 resulted in the induction of apoptosis at 6 h. Mitochondrial dysfunction and ROS imbalance induced the intrinsic apoptotic pathway induction following 4NC exposures. While increased ROS is caused by LG exposure in lung cells, 4NC is a marker of concern during BB emissions, as we observed apoptosis and high mitochondrial ROS in both lung cells at atmospherically-relevant aerosol concentrations. It may be associated with higher airway or inhalation pathologies in higher BBA emissions, such as wildfires or during wood combustion. [Display omitted] •Mitochondrial dysfunction occurred in 4NC-exposed BEAS-2B and A549 cells.•IC50 values for 4NC-exposed cells were lower than for LG-exposed cells.•LG-exposed BEAS-2B cells revealed mitochondrial ROS build-up at 12–24 h.•4NC-exposed BEAS-2B cells undergo apoptosis at 6–48 h.
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Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β-D-glucopyranose). Atmospheric chemical aging of BB-derived aerosol (BBA) in the presence of nitrogen oxides (NOx) can yield nitro-aromatic compounds, including 4-nitrocatechol (4NC). There is building evidence that NOx-mediated chemical aging of BBA poses a more serious exposure effect than primary pyrolysis emissions. This study provides a comparative toxicological assessment following the exposure to important BBA marker compounds in human lung cells (i.e., A549 and BEAS-2B) to determine whether aromatic 4NC is more toxic than BBA-bound anhydrous carbohydrate (i.e., LG). We determined inhibitory concentration-50 (IC50) and examined reactive oxygen species (ROS) changes, mitochondrial dysfunction, and apoptosis induction in the two cell lines following exposure to LG and 4NC in a dose-response manner. In the BEAS-2B cells, estimated IC50 values for 4NC were 33 and 8.8 μg mL−1, and for LG were 2546 and ∼3 × 107 μg mL−1 at 24 h and 48 h of exposure, respectively. A549 cells exhibited a much higher IC50 value than BEAS-2B cells. LG exposures resulted in mitochondrial stress with viability inhibition, but cells recovered with increasing exposure time. 4NC exposures at 200 μg mL−1 resulted in the induction of apoptosis at 6 h. Mitochondrial dysfunction and ROS imbalance induced the intrinsic apoptotic pathway induction following 4NC exposures. While increased ROS is caused by LG exposure in lung cells, 4NC is a marker of concern during BB emissions, as we observed apoptosis and high mitochondrial ROS in both lung cells at atmospherically-relevant aerosol concentrations. It may be associated with higher airway or inhalation pathologies in higher BBA emissions, such as wildfires or during wood combustion. [Display omitted] •Mitochondrial dysfunction occurred in 4NC-exposed BEAS-2B and A549 cells.•IC50 values for 4NC-exposed cells were lower than for LG-exposed cells.•LG-exposed BEAS-2B cells revealed mitochondrial ROS build-up at 12–24 h.•4NC-exposed BEAS-2B cells undergo apoptosis at 6–48 h.</description><identifier>ISSN: 0269-7491</identifier><identifier>ISSN: 1873-6424</identifier><identifier>EISSN: 1873-6424</identifier><identifier>DOI: 10.1016/j.envpol.2024.125173</identifier><identifier>PMID: 39442609</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>A549 Cells ; Aerosols ; Air Pollutants - toxicity ; Apoptosis ; Apoptosis - drug effects ; Biomass ; Biomass burning aerosol ; breathing ; Catechols - chemistry ; Catechols - toxicity ; Cell Line ; combustion ; cytotoxicity ; dose response ; exposure duration ; Glucose - analogs &amp; derivatives ; Humans ; Inhibitory concentration-50 ; Lung - drug effects ; lungs ; mitochondria ; Mitochondria - drug effects ; Nitroaromatics ; nitrogen ; pollution ; pyrolysis ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; risk ; sugars ; toxicity testing ; viability ; wood</subject><ispartof>Environmental pollution (1987), 2024-12, Vol.363 (Pt 2), p.125173, Article 125173</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. 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All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c274t-28a12e81abf93d0da9f61f4c8706524e2c0464b778cc511165df0b81e4c53f683</cites><orcidid>0000-0002-7396-9571 ; 0000-0001-6539-888X ; 0000-0002-6833-1450 ; 0000-0002-5197-0635 ; 0000-0002-5785-9751 ; 0000-0003-3389-9318</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0269749124018906$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39442609$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khan, Faria</creatorcontrib><creatorcontrib>Kwapiszewska, Karina</creatorcontrib><creatorcontrib>Romero, Alicia M.</creatorcontrib><creatorcontrib>Rudzinski, Krzysztof</creatorcontrib><creatorcontrib>Gil-Casanova, Domingo</creatorcontrib><creatorcontrib>Surratt, Jason D.</creatorcontrib><creatorcontrib>Szmigielski, Rafal</creatorcontrib><title>Evidence for cytotoxicity and mitochondrial dysfunction in human lung cells exposed to biomass burning aerosol constituents: Levoglucosan and 4-nitrocatechol</title><title>Environmental pollution (1987)</title><addtitle>Environ Pollut</addtitle><description>Biomass burning (BB) emissions are one of the largest sources of carbonaceous aerosol, posing a significant risk as an airway irritant. Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β-D-glucopyranose). Atmospheric chemical aging of BB-derived aerosol (BBA) in the presence of nitrogen oxides (NOx) can yield nitro-aromatic compounds, including 4-nitrocatechol (4NC). There is building evidence that NOx-mediated chemical aging of BBA poses a more serious exposure effect than primary pyrolysis emissions. This study provides a comparative toxicological assessment following the exposure to important BBA marker compounds in human lung cells (i.e., A549 and BEAS-2B) to determine whether aromatic 4NC is more toxic than BBA-bound anhydrous carbohydrate (i.e., LG). We determined inhibitory concentration-50 (IC50) and examined reactive oxygen species (ROS) changes, mitochondrial dysfunction, and apoptosis induction in the two cell lines following exposure to LG and 4NC in a dose-response manner. In the BEAS-2B cells, estimated IC50 values for 4NC were 33 and 8.8 μg mL−1, and for LG were 2546 and ∼3 × 107 μg mL−1 at 24 h and 48 h of exposure, respectively. A549 cells exhibited a much higher IC50 value than BEAS-2B cells. LG exposures resulted in mitochondrial stress with viability inhibition, but cells recovered with increasing exposure time. 4NC exposures at 200 μg mL−1 resulted in the induction of apoptosis at 6 h. Mitochondrial dysfunction and ROS imbalance induced the intrinsic apoptotic pathway induction following 4NC exposures. While increased ROS is caused by LG exposure in lung cells, 4NC is a marker of concern during BB emissions, as we observed apoptosis and high mitochondrial ROS in both lung cells at atmospherically-relevant aerosol concentrations. It may be associated with higher airway or inhalation pathologies in higher BBA emissions, such as wildfires or during wood combustion. 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Important BB markers include wood pyrolysis emissions, such as levoglucosan (LG) that is an anhydrous sugar bearing a six-carbon ring structure (i.e., 1,6-anhydro-β-D-glucopyranose). Atmospheric chemical aging of BB-derived aerosol (BBA) in the presence of nitrogen oxides (NOx) can yield nitro-aromatic compounds, including 4-nitrocatechol (4NC). There is building evidence that NOx-mediated chemical aging of BBA poses a more serious exposure effect than primary pyrolysis emissions. This study provides a comparative toxicological assessment following the exposure to important BBA marker compounds in human lung cells (i.e., A549 and BEAS-2B) to determine whether aromatic 4NC is more toxic than BBA-bound anhydrous carbohydrate (i.e., LG). We determined inhibitory concentration-50 (IC50) and examined reactive oxygen species (ROS) changes, mitochondrial dysfunction, and apoptosis induction in the two cell lines following exposure to LG and 4NC in a dose-response manner. In the BEAS-2B cells, estimated IC50 values for 4NC were 33 and 8.8 μg mL−1, and for LG were 2546 and ∼3 × 107 μg mL−1 at 24 h and 48 h of exposure, respectively. A549 cells exhibited a much higher IC50 value than BEAS-2B cells. LG exposures resulted in mitochondrial stress with viability inhibition, but cells recovered with increasing exposure time. 4NC exposures at 200 μg mL−1 resulted in the induction of apoptosis at 6 h. Mitochondrial dysfunction and ROS imbalance induced the intrinsic apoptotic pathway induction following 4NC exposures. While increased ROS is caused by LG exposure in lung cells, 4NC is a marker of concern during BB emissions, as we observed apoptosis and high mitochondrial ROS in both lung cells at atmospherically-relevant aerosol concentrations. It may be associated with higher airway or inhalation pathologies in higher BBA emissions, such as wildfires or during wood combustion. [Display omitted] •Mitochondrial dysfunction occurred in 4NC-exposed BEAS-2B and A549 cells.•IC50 values for 4NC-exposed cells were lower than for LG-exposed cells.•LG-exposed BEAS-2B cells revealed mitochondrial ROS build-up at 12–24 h.•4NC-exposed BEAS-2B cells undergo apoptosis at 6–48 h.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>39442609</pmid><doi>10.1016/j.envpol.2024.125173</doi><orcidid>https://orcid.org/0000-0002-7396-9571</orcidid><orcidid>https://orcid.org/0000-0001-6539-888X</orcidid><orcidid>https://orcid.org/0000-0002-6833-1450</orcidid><orcidid>https://orcid.org/0000-0002-5197-0635</orcidid><orcidid>https://orcid.org/0000-0002-5785-9751</orcidid><orcidid>https://orcid.org/0000-0003-3389-9318</orcidid><oa>free_for_read</oa></addata></record>
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ispartof Environmental pollution (1987), 2024-12, Vol.363 (Pt 2), p.125173, Article 125173
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subjects A549 Cells
Aerosols
Air Pollutants - toxicity
Apoptosis
Apoptosis - drug effects
Biomass
Biomass burning aerosol
breathing
Catechols - chemistry
Catechols - toxicity
Cell Line
combustion
cytotoxicity
dose response
exposure duration
Glucose - analogs & derivatives
Humans
Inhibitory concentration-50
Lung - drug effects
lungs
mitochondria
Mitochondria - drug effects
Nitroaromatics
nitrogen
pollution
pyrolysis
Reactive oxygen species
Reactive Oxygen Species - metabolism
risk
sugars
toxicity testing
viability
wood
title Evidence for cytotoxicity and mitochondrial dysfunction in human lung cells exposed to biomass burning aerosol constituents: Levoglucosan and 4-nitrocatechol
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