Signal Transduction and Cytokine Expression in Particulate Matter (PM)-Induced Airway Remodeling

Author(s):  
Dianne Walters ◽  
James Bonner
Life ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 260
Author(s):  
Sun Woo Jin ◽  
Gi Ho Lee ◽  
Min Jung Jang ◽  
Gyeong Eun Hong ◽  
Jae Young Kim ◽  
...  

Several air pollution components such as sulfur dioxide, ozone, nitrogen dioxide, and diesel exhaust particulate matter (DEPM) have been linked to the development of asthma. In this study, we investigated the therapeutic potential of three lactic acid bacteria species, Lactobacillus plantarum GREEN CROSS Wellbeing (GCWB)1001, Pediococcus acidilactici GCWB1085, and Lactobacillus rhamnosus GCWB1156, in preventing DEPM-exacerbated asthma in mice. BALB/c mice were first sensitized with ovalbumin (OVA) and were either challenged with OVA or DEPM (DEPM-exacerbated asthma model) by intranasal instillation. All three strains showed no hemolytic activity, suggesting a good safety profile. Oral administration of lactic acid bacteria reduced OVA + DEPM-induced inflammatory infiltration, goblet cell hyperplasia, airway remodeling, and the levels of proinflammatory cytokines and chemokines in bronchoalveolar lavage fluid (BALF). The probiotics also attenuated OVA + DEPM-induced immunoglobulin E (IgE) levels in serum and in BALF, and significantly reduced caspase-3 activity, total collagen level, and matrix metalloproteinase (MMP)-9 activity. In conclusion, lactic acid bacteria such as L. plantarum GCWB1001, P. acidilactici GCWB1085, and L. rhamnosus treatment in mice with asthma showed significant efficacy in preventing lung inflammation exacerbated by DEPM administration.


Alcohol ◽  
2012 ◽  
Vol 46 (2) ◽  
pp. 178
Author(s):  
P.T. Thevenot ◽  
J. Saravia ◽  
T. Ahlert ◽  
M.A. Kelly ◽  
T.R. Dugas ◽  
...  

2010 ◽  
Vol 131 (1) ◽  
pp. 24-32 ◽  
Author(s):  
Cornelia M. Spies ◽  
Timo Gaber ◽  
Martin Hahne ◽  
Lydia Naumann ◽  
Robert Tripmacher ◽  
...  

2016 ◽  
Vol 64 (4) ◽  
pp. 970.2-971
Author(s):  
X Wu ◽  
X Xu ◽  
JG Garcia ◽  
T Wang

IntroductionParticulate matter (PM) is significantly associated with cardiopulmonary morbidity and mortality. We previously demonstrated that PM induces endothelial barrier disruption via reactive oxygen species (ROS)-dependent mechanisms. This study is focused on characterization of PM-regulated endothelial dysfunction via connexin43 (Cx43), a Gap junction protein. Gap junction is designated as intercellular channel which allows cells to communicate with each other, share nutrients, and transfer chemical or electrical signals, in turn, enables cells in a tissue to function in a coordinated manner.Methods and ResultsCx43 protein levels were evaluated by western blotting, and band density quantified using MyImageAnalysis. Real-time PCR was conducted to determine Cx43 mRNA levels. Human pulmonary artery endothelial cell (EC) barrier function was measured using the electrical cell-substrate impedance sensing (ECIS) system (Applied Biophysics) that provides a readout of transendothelial electrical resistance (TER). PM sample (0.1–0.3 µm of aerodynamic diameter) was collected (April of 2005) from the Ft. McHenry Tunnel, Baltimore, MD using a high-volume cyclone collector. PM (100 µg/ml) induced time-dependent increases in EC Cx43 mRNA levels (∼5 fold increase at 4 hr) and protein expression which was attenuated by N-acetyl-cysteine (NAC, 5 mM, 1 hr pretreatment), an ROS scavenger. Unlike Cx43, Cx37, another connexin expressed in ECs, remained unaltered by PM challenge. In addition, EC pretreatment with a Cx43 inhibitor, connexin-mimetic peptide Gap27 (500 µM, 2 hr pretreatment), significantly attenuated PM-reduced TER reduction by 45%, suggesting a central role of Cx43 in PM-induced lung EC barrier integrity disruption and signal transduction.ConclusionsOur results suggest Cx43 as a key and novel participant in PM-mediated signal transduction that results in loss of vascular barrier integrity. Cx43 may serve as a therapeutic target in PM-induced cardiopulmonary toxicities.


Oncotarget ◽  
2017 ◽  
Vol 8 (28) ◽  
pp. 46312-46325 ◽  
Author(s):  
Zhe Cheng ◽  
Ling-Ling Dai ◽  
Xi Wang ◽  
Liu-Qun Jia ◽  
Xiao-Gang Jing ◽  
...  

2014 ◽  
Vol 30 (7) ◽  
pp. 836-851 ◽  
Author(s):  
Zana Sijan ◽  
Dagmara S. Antkiewicz ◽  
Jongbae Heo ◽  
Norman Y. Kado ◽  
James J. Schauer ◽  
...  

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