Ghio Andrew J, Soukup Joleen M, Dailey Lisa A, Tong Haiyan, Kesic Matthew J, Budinger G R Scott, Mutlu Gökhan M
US Environmental Protection Agency , Chapel Hill, North Carolina 27599, United States.
Physician Assistant Program, Methodist University , Fayetteville, North Carolina 28311, United States.
Chem Res Toxicol. 2015 Nov 16;28(11):2104-11. doi: 10.1021/acs.chemrestox.5b00270. Epub 2015 Oct 22.
The biological effect of an inorganic particle (i.e., silica) can be associated with a disruption in cell iron homeostasis. Organic compounds included in particles originating from combustion processes can also complex sources of host cell iron to disrupt metal homeostasis. We tested the postulate that (1) wood smoke particle (WSP) sequesters host cell iron resulting in a disruption of metal homeostasis, (2) this loss of essential metal results in both an oxidative stress and biological effect in respiratory epithelial cells, and (3) humic-like substances (HULIS), a component of WSP, have a capacity to appropriate cell iron and initiate a biological effect. BEAS-2B cells exposed to WSP resulted in diminished concentrations of mitochondrial (57)Fe, whereas preincubation with ferric ammonium citrate (FAC) prevented significant mitochondrial iron loss after such exposure. Cellular oxidant generation was increased after WSP exposure, but this signal was diminished by coincubation with FAC. Similarly, exposure of BEAS-2B cells to 100 μg/mL WSP activated mitogen-activated protein (MAP) kinases, elevated NF-E2-related factor 2/antioxidant responsive element (Nrf2 ARE) expression, and provoked interleukin (IL)-6 and IL-8 release, but all these changes were diminished by coincubation with FAC. The biological response to WSP was reproduced by exposure to 100 μg/mL humic acid, a polyphenol comparable to HULIS included in the WSP that complexes iron. We conclude that (1) the biological response following exposure to WSP is associated with sequestration of cell iron by the particle, (2) increasing available iron in the cell diminished the biological effects after particle exposure, and (3) HULIS included in WSP can sequester the metal initiating the cell response.
无机颗粒(如二氧化硅)的生物学效应可能与细胞铁稳态的破坏有关。来自燃烧过程的颗粒中所含的有机化合物也可以与宿主细胞铁源络合,从而破坏金属稳态。我们验证了以下假设:(1)木烟颗粒(WSP)螯合宿主细胞铁,导致金属稳态破坏;(2)这种必需金属的损失导致呼吸道上皮细胞产生氧化应激和生物学效应;(3)腐殖质样物质(HULIS)是WSP的一种成分,具有摄取细胞铁并引发生物学效应的能力。暴露于WSP的BEAS-2B细胞线粒体(57)Fe浓度降低,而用柠檬酸铁铵(FAC)预孵育可防止暴露后线粒体铁的显著损失。WSP暴露后细胞氧化剂生成增加,但与FAC共同孵育可减弱该信号。同样,将BEAS-2B细胞暴露于100μg/mL WSP会激活丝裂原活化蛋白(MAP)激酶,提高核因子E2相关因子2/抗氧化反应元件(Nrf2 ARE)的表达,并引发白细胞介素(IL)-6和IL-8的释放,但与FAC共同孵育可减弱所有这些变化。暴露于100μg/mL腐殖酸可重现对WSP的生物学反应,腐殖酸是一种与WSP中包含的能络合铁的HULIS相当的多酚。我们得出以下结论:(1)暴露于WSP后的生物学反应与颗粒对细胞铁的螯合有关;(2)增加细胞中可利用的铁可减弱颗粒暴露后的生物学效应;(3)WSP中包含的HULIS可螯合金属,引发细胞反应。