Inflammatory, Oxidative Stress and Small Cellular Particle Response in HUVEC Induced by Debris from Endoprosthesis Processing

Author:

Jan Zala1,Hočevar Matej2,Kononenko Veno3ORCID,Michelini Sara3ORCID,Repar Neža3,Caf Maja45,Kocjančič Boštjan678,Dolinar Drago678,Kralj Slavko45ORCID,Makovec Darko4,Iglič Aleš910ORCID,Drobne Damjana3ORCID,Jenko Monika7,Kralj-Iglič Veronika1

Affiliation:

1. University of Ljubljana, Faculty of Health Sciences, Laboratory of Clinical Biophysics, SI-1000 Ljubljana, Slovenia

2. Institute of Metals and Technology, SI-1000 Ljubljana, Slovenia

3. University of Ljubljana, Biotechnical Faculty, Nanobiology Group, SI-1000 Ljubljana, Slovenia

4. Department for Materials Synthesis, Jožef Stefan Institute, SI-1000 Ljubljana, Slovenia

5. University of Ljubljana, Faculty of Pharmacy, SI-1000 Ljubljana, Slovenia

6. University of Ljubljana, Faculty of Medicine, Chair of Orthopaedics, SI-1000 Ljubljana, Slovenia

7. MD-RI Institute for Materials Research in Medicine, SI-1000 Ljubljana, Slovenia

8. Department of Orthopaedic Surgery, University Medical Centre Ljubljana, SI-1000 Ljubljana, Slovenia

9. University of Ljubljana, Faculty of Electrical Engineering, Laboratory of Physics, SI-1000 Ljubljana, Slovenia

10. University of Ljubljana, Faculty of Medicine, Laboratory of Clinical Biophysics, SI-1000 Ljubljana, Slovenia

Abstract

We studied inflammatory and oxidative stress-related parameters and cytotoxic response of human umbilical vein endothelial cells (HUVEC) to a 24 h treatment with milled particles simulating debris involved in sandblasting of orthopedic implants (OI). We used different abrasives (corundum—(Al2O3), used corundum retrieved from removed OI (u. Al2O3), and zirconia/silica composite (ZrO2/SiO2)). Morphological changes were observed by scanning electron microscopy (SEM). Concentration of Interleukins IL-6 and IL-1β and Tumor Necrosis Factor α (TNF)-α was assessed by enzyme-linked immunosorbent assay (ELISA). Activity of Cholinesterase (ChE) and Glutathione S-transferase (GST) was measured by spectrophotometry. Reactive oxygen species (ROS), lipid droplets (LD) and apoptosis were measured by flow cytometry (FCM). Detachment of the cells from glass and budding of the cell membrane did not differ in the treated and untreated control cells. Increased concentration of IL-1β and of IL-6 was found after treatment with all tested particle types, indicating inflammatory response of the treated cells. Increased ChE activity was found after treatment with u. Al2O3 and ZrO2/SiO2. Increased GST activity was found after treatment with ZrO2/SiO2. Increased LD quantity but not ROS quantity was found after treatment with u. Al2O3. No cytotoxicity was detected after treatment with u. Al2O3. The tested materials in concentrations added to in vitro cell lines were found non-toxic but bioactive and therefore prone to induce a response of the human body to OI.

Funder

Slovenian Research Agency

EUREKA IMPLANT BLASTER

National Research, Development and Innovation Office

Publisher

MDPI AG

Subject

General Materials Science

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