The Effects of Vitamin E Analogues α-Tocopherol and γ-Tocotrienol on the Human Osteocyte Response to Ultra-High Molecular Weight Polyethylene Wear Particles

被引:2
作者
Ormsby, Renee T. [1 ]
Hosaka, Kunihiro [1 ]
Evdokiou, Andreas [2 ]
Odysseos, Andreani [3 ]
Findlay, David M. [1 ,4 ]
Solomon, Lucian B. [1 ,4 ]
Atkins, Gerald J. [1 ]
机构
[1] Univ Adelaide, Ctr Orthopaed & Trauma Res, Biomed Orthopaed Res Grp, Adelaide, SA 5000, Australia
[2] Univ Adelaide, Basil Hetzel Inst, Discipline Surg, Adelaide, SA 5000, Australia
[3] Univ Cyprus, Dept Biomed Res, Lab Nanobiotechnol, EPOS Iasis,R&D, CY-1678 Nicosia, Cyprus
[4] Royal Adelaide Hosp, Dept Orthopaed & Trauma, Adelaide, SA 5000, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
osteocyte; wear particle; polyethylene; tocopherol; tocotrienol; vitamin E; BONE-MINERAL DENSITY; OXIDATIVE STRESS; UHMWPE; OSTEOBLASTS; INDUCTION; RADIATION; CELLS;
D O I
10.3390/prosthesis4030039
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Polyethylene (PE) liners are a common bearing surface of orthopaedic prostheses. Wear particles of ultra-high molecular weight PE (UHMWPE) contribute to periprosthetic osteolysis, a major cause of aseptic loosening. Vitamin E is added to some PE liners to prevent oxidative degradation. Osteocytes, an important cell type for controlling both bone mineralisation and bone resorption, have been shown to respond UHMWPE particles by upregulating pro-osteoclastogenic and osteocytic osteolysis. Here, we examined the effects of the vitamin E analogues alpha-tocopherol and gamma-tocotrienol alone or in the context of UHMWPE particles on human osteocyte gene expression and mineralisation behaviour. Human osteoblasts differentiated to an osteocyte-like stage were exposed to UHMWPE wear particles in the presence or absence of either alpha-Tocopherol or gamma-Tocotrienol. Both alpha-Tocopherol and gamma-Tocotrienol induced antioxidant-related gene expression. UHMWPE particles independently upregulated antioxidant gene expression, suggesting an effect of wear particles on oxidative stress. Both vitamin E analogues strongly induced OPG mRNA expression and gamma-Tocotrienol also inhibited RANKL mRNA expression, resulting in a significantly reduced RANKL:OPG mRNA ratio (p < 0.01) overall. UHMWPE particles reversed the suppressive effect of alpha-Tocopherol but not of gamma-Tocotrienol on this pro-osteoclastogenic index. UHMWPE particles also upregulated osteocytic-osteolysis related gene expression. Vitamin E analogues alone or in combination with UHMWPE particles also resulted in upregulation of these genes. Consistent with this, both vitamin E analogues promoted calcium release from mineralised cultures of osteocyte-like cells. Our findings suggest that while vitamin E may suppress osteocyte support of osteoclastogenesis in the presence of UHMWPE particles, the antioxidant effect may induce osteocytic osteolysis, which could promote periprosthetic osteolysis. It will be important to conduct further studies of vitamin E to determine the long-term effects of its inclusion in prosthetic materials.
引用
收藏
页码:480 / 489
页数:10
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