2018European Cells and MaterialsOpen access

TiO2 nanoparticles can selectively bind CXCL8 impacting on neutrophil chemotaxis

Joanna Batt, Mike Milward, Iain Chapple, Melissa M. Grant, Scott J. Roberts, Owen Addison

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Abstract

The interaction between TiO 2 nanoparticles (NPs) and inflammatory cytokines, including CXCL8, a clinically relevant pro-inflammatory chemokine, was investigated.TiO 2 is present in tissues adjacent to failing implanted Ti (titanium) devices.TiO 2 NPs were shown to bind to CXCL8 in vitro, causing perturbation of quantification of CXCL8 by ELISA, in both simple and complex protein panels, in a dose-dependent manner.Binding between TiO 2 NPs and CXCL8 was demonstrated by protein gel electrophoresis.TiO 2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO 2 NPs and CXCL8 is likely to be clinically relevant.The results of this study disputed the applicability of detection of CXCL8 by ELISA in systems where TiO 2 NPs were present.Clinically, the disruption of neutrophil chemotaxis due to CXCL8 binding to TiO 2 NPs might result in a hampered inflammatory response.

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What this paper is about

The interaction between TiO 2 nanoparticles (NPs) and inflammatory cytokines, including CXCL8, a clinically relevant pro-inflammatory chemokine, was investigated.TiO 2 is present in tissues adjacent to failing implanted Ti (titanium) devices.TiO 2 NPs were shown to bind to CXCL8 in vitro, causing perturbation of quantification of CXCL8 by ELISA, in both simple and complex protein panels, in a dose-dependent manner.Binding between TiO 2 NPs and CXCL8 was demonstrated by protein gel electrophoresis.TiO 2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO 2 NPs and CXCL8 is likely to be clinically relevant.The results of this study disputed the applicability of detection of CXCL8 by ELISA in systems where TiO 2 NPs were present.Clinically, the disruption of neutrophil chemotaxis due to CXCL8 binding to TiO 2 NPs might result in a hampered inflammatory response.

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Available abstract

The interaction between TiO 2 nanoparticles (NPs) and inflammatory cytokines, including CXCL8, a clinically relevant pro-inflammatory chemokine, was investigated.TiO 2 is present in tissues adjacent to failing implanted Ti (titanium) devices.TiO 2 NPs were shown to bind to CXCL8 in vitro, causing perturbation of quantification of CXCL8 by ELISA, in both simple and complex protein panels, in a dose-dependent manner.Binding between TiO 2 NPs and CXCL8 was demonstrated by protein gel electrophoresis.TiO 2 NPs were also shown to inactivate the chemoattractant property of CXCL8 in a dose-dependent manner, suggesting that the binding between TiO 2 NPs and CXCL8 is likely to be clinically relevant.The results of this study disputed the applicability of detection of CXCL8 by ELISA in systems where TiO 2 NPs were present.Clinically, the disruption of neutrophil chemotaxis due to CXCL8 binding to TiO 2 NPs might result in a hampered inflammatory response.

Key concepts: Interleukin 8, Chemotaxis, Chemokine, Chemistry, Titanium, Inflammation, Biophysics, Materials science

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