TY - JOUR
T1 - Acid-treated multi-walled carbon nanotubes coated with lung surfactant protein SP-A do not induce a lung inflammatory response
AU - Salvador-Morales, Carolina
AU - Khan, Zara
AU - Zamory, Justin
AU - Tran, Viet
AU - Cedeno, Andrew
AU - Umanzor-Alvarez, Jose
AU - Kishore, Uday
AU - Sim, Robert B.
PY - 2013/6
Y1 - 2013/6
N2 - The potential toxicity of carbon nanotubes (CNTs) in the lungs has not been widely investigated at the protein level. Previous studies have focused on addressing pulmonary toxicity primarily at the tissue and cellular levels. However, studying the interaction between carbon nanotubes and the lung surfactant proteins A (SP-A) and D (SP-D), two versatile and potent innate immune molecules in the lungs, can yield important information about the mechanisms involved in lung toxicity. Here, we investigated whether SP-A-coated acid treated multi-walled carbon nanotubes (MWCNTox) induced an inflammatory response. We found that although SP-A coated MWCNTox were avidly taken up by alveolar macrophages, they did not induce an inflammatory response as measured by the enhancement of levels of nitric oxide, a key marker for inflammation, when carbon nanotubes were incubated with IFN-γ primed alveolar macrophages. Thus, the binding of SP-A to carbon nanotubes does not trigger inflammation.
AB - The potential toxicity of carbon nanotubes (CNTs) in the lungs has not been widely investigated at the protein level. Previous studies have focused on addressing pulmonary toxicity primarily at the tissue and cellular levels. However, studying the interaction between carbon nanotubes and the lung surfactant proteins A (SP-A) and D (SP-D), two versatile and potent innate immune molecules in the lungs, can yield important information about the mechanisms involved in lung toxicity. Here, we investigated whether SP-A-coated acid treated multi-walled carbon nanotubes (MWCNTox) induced an inflammatory response. We found that although SP-A coated MWCNTox were avidly taken up by alveolar macrophages, they did not induce an inflammatory response as measured by the enhancement of levels of nitric oxide, a key marker for inflammation, when carbon nanotubes were incubated with IFN-γ primed alveolar macrophages. Thus, the binding of SP-A to carbon nanotubes does not trigger inflammation.
KW - Alveolar Macrophages
KW - Carbon Nanotubes
KW - Lung Surfactant
KW - Nitric Oxide
KW - SP-A
KW - SP-D
UR - http://www.scopus.com/inward/record.url?scp=84889042644&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84889042644&partnerID=8YFLogxK
U2 - 10.1166/jamr.2013.1143
DO - 10.1166/jamr.2013.1143
M3 - Article
AN - SCOPUS:84889042644
SN - 2156-7573
VL - 8
SP - 93
EP - 99
JO - Journal of Advanced Microscopy Research
JF - Journal of Advanced Microscopy Research
IS - 2
ER -