Aggravation of inflammatory response by costimulation with titanium particles and mechanical perturbations in osteoblast- and macrophage-like cells

• Published in: American Journal of Physiology: Cell Physiology 2013-03, Vol.304 (5), p.C431-C439
• Main Authors: Lee, Heon Goo, Hsu, Anny, Goto, Hana, Nizami, Saqib, Lee, Jonathan H, Cadet, Edwin R, Tang, Peter, Shaji, Roya, Chandhanayinyong, Chandhanarat, Kweon, Seok Hyun, Oh, Daniel S, Tawfeek, Hesham, Lee, Francis Y
• Format: Article
• Language: English
• Subjects: Actins - metabolism; Animals; Bones; Cell Line; Cell Membrane - drug effects; Cell Membrane - genetics; Cell Membrane - metabolism; Cells; Cellular Microenvironment - drug effects; Cellular Microenvironment - genetics; Cytokines; Cytokines - genetics; Cytokines - metabolism; Gene expression; Gene Expression - drug effects; Gene Expression - genetics; Inflammation - chemically induced; Inflammation - genetics; Inflammation - metabolism; Macrophages - drug effects; Macrophages - metabolism; Male; MAP Kinase Signaling System - drug effects; MAP Kinase Signaling System - genetics; Mice; Mice, Inbred C57BL; Osteoblasts - drug effects; Osteoblasts - metabolism; Phagocytosis - drug effects; Phagocytosis - genetics; Prostheses and Implants; Tissues; Titanium; Titanium - toxicity; Transplants & implants
• ISSN: 0363-6143; 1522-1563
• DOI: 10.1152/ajpcell.00202.2012

The interface between bone tissue and metal implants undergoes various types of mechanical loading, such as strain, compression, fluid pressure, and shear stress, from daily activities. Such mechanical perturbations create suboptimal environments at the host bone-implant junction, causing an accumulation of wear particles and debilitating osseous integration, potentially leading to implant failure. While many studies have focused on the effect of particles on macrophages or osteoprogenitor cells, differential and combined effects of mechanical perturbations and particles on such cell types have not been extensively studied. In this study, macrophages and osteoprogenitor cells were subjected to physiological and superphysiological mechanical stimuli in the presence and absence of Ti particles with the aim of simulating various microenvironments of the host bone-implant junction. Macrophages and osteoprogenitor cells were capable of engulfing Ti particles through actin remodeling and also exhibited changes in mRNA levels of proinflammatory cytokines under certain conditions. In osteoprogenitor cells, superphysiological strain increased proinflammatory gene expression; in macrophages, such mechanical perturbations did not affect gene expression. We confirmed that this phenomenon in osteoprogenitor cells occurred via activation of the ERK1/2 signaling pathway as a result of damage to the cytoplasmic membrane. Furthermore, AZD6244, a clinically relevant inhibitor of the ERK1/2 pathway, mitigated particle-induced inflammatory gene expression in osteoprogenitor cells and macrophages. This study provides evidence of more inflammatory responses under mechanical strains in osteoprogenitor cells than macrophages. Phagocytosis of particles and mechanical perturbation costimulate the ERK1/2 pathway, leading to expression of proinflammatory genes.