Adsorbed plasma proteins modulate the effects of single-walled carbon nanotubes on neutrophils in blood. / Vlasova, I.I.; Mikhalchik, E.V.; Barinov, N.A.; Kostevich, V.A.; Smolina, N.V.; Klinov, D.V.; Sokolov, A.V.
In: Nanomedicine: Nanotechnology, Biology, and Medicine, Vol. 12, No. 6, 2016, p. 1615–1625.Research output: Contribution to journal › Article
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TY - JOUR
T1 - Adsorbed plasma proteins modulate the effects of single-walled carbon nanotubes on neutrophils in blood
AU - Vlasova, I.I.
AU - Mikhalchik, E.V.
AU - Barinov, N.A.
AU - Kostevich, V.A.
AU - Smolina, N.V.
AU - Klinov, D.V.
AU - Sokolov, A.V.
PY - 2016
Y1 - 2016
N2 - Proteins adsorbed on a surface may affect the interaction of this surface with cells. Here, we studied the binding of human serum albumin (HSA), fibrinogen (FBG) and immunoglobulin G (IgG) to PEGylated single-walled carbon nanotubes (PEG-SWCNTs) and evaluated the impact of PEG-SWCNT treated by these proteins on neutrophils in whole blood samples. Measurements of adsorption parameters revealed tight binding of proteins to PEG-SWCNTs. AFM was employed to directly observe protein binding to side walls of PEG-SWCNTs. Fluorescein-labeled IgG was used to ascertain the stability of PEG-SWCNT-IgG complexes in plasma. In blood samples, all plasma proteins mitigated damage of neutrophils observed just after blood exposure to PEG-SWCNTs, while only treatment of PEG-SWCNTs with IgG resulted in dose- and time-dependent enhancement of CNT-induced neutrophil activation and in potentiation of oxidative stress. Our study demonstrates the ability of adsorbed plasma proteins to influence neutrophil response caused by PEG-SWCNTs
AB - Proteins adsorbed on a surface may affect the interaction of this surface with cells. Here, we studied the binding of human serum albumin (HSA), fibrinogen (FBG) and immunoglobulin G (IgG) to PEGylated single-walled carbon nanotubes (PEG-SWCNTs) and evaluated the impact of PEG-SWCNT treated by these proteins on neutrophils in whole blood samples. Measurements of adsorption parameters revealed tight binding of proteins to PEG-SWCNTs. AFM was employed to directly observe protein binding to side walls of PEG-SWCNTs. Fluorescein-labeled IgG was used to ascertain the stability of PEG-SWCNT-IgG complexes in plasma. In blood samples, all plasma proteins mitigated damage of neutrophils observed just after blood exposure to PEG-SWCNTs, while only treatment of PEG-SWCNTs with IgG resulted in dose- and time-dependent enhancement of CNT-induced neutrophil activation and in potentiation of oxidative stress. Our study demonstrates the ability of adsorbed plasma proteins to influence neutrophil response caused by PEG-SWCNTs
KW - Albumin
KW - Fibrinogen
KW - Immunoglobulin G
KW - Myeloperoxidase
KW - Neutrophil activation
KW - PEGylated carbon nanotubes
U2 - 10.1016/j.nano.2016.02.012
DO - 10.1016/j.nano.2016.02.012
M3 - Article
VL - 12
SP - 1615
EP - 1625
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
SN - 1549-9634
IS - 6
ER -
ID: 7564580