New insight into the mechanism of hip prosthesis loosening: effect of titanium debris size on osteoblast function
- PMID: 15013079
- DOI: 10.1016/S0736-0266(03)00167-0
New insight into the mechanism of hip prosthesis loosening: effect of titanium debris size on osteoblast function
Abstract
The incidence of rheumatoid arthritis and osteoarthritis is on the rise due to our expanding elderly population. Total joint arthroplasty is the most successful, prevalent treatment modality for these and other degenerative hip conditions. Despite the wide array of prosthetic devices commercially available, hip prostheses share a common problem with a gradual and then accelerating loss of bone tissue and bone-implant interface integrity, followed by implant instability and loosening. Implant failure is largely the result of inevitable wear of the device and generation of wear debris. To provide information for the development of improved prosthetic wear characteristics, we examined the effects of size-separated titanium particles on bone forming cell populations. We demonstrate unequivocally that particle size is a critical factor in the function, proliferation, and viability of bone-forming osteoblasts in vitro. In addition, we have elucidated the time-dependent distribution of the phagocytosed particles within the osteoblast, indicating an accumulation of particles in the perinuclear area of the affected cells. The report finds that particle size is a critical factor in changes in the bone formation-related functions of osteoblasts exposed to simulate wear debris, and that 1.5-4 microm titanium particles have the greatest effect on osteoblast proliferation and viability in vitro. The size of titanium particles generated through wear of a prosthetic device may be an important consideration in the development of superior implant technology.
Similar articles
-
Alterations in the adhesion behavior of osteoblasts by titanium particle loading: inhibition of cell function and gene expression.Biorheology. 2001;38(2-3):161-83. Biorheology. 2001. PMID: 11381173
-
Response of human osteoblasts exposed to wear particles generated at the interface of total hip stems and bone cement.J Biomed Mater Res A. 2009 May;89(2):370-8. doi: 10.1002/jbm.a.31996. J Biomed Mater Res A. 2009. PMID: 18431768
-
[Influence of different-sized titanium particles loading on osteoblastic differentiation and mineralization].Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2005 Feb;22(1):30-4. Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2005. PMID: 15762109 Chinese.
-
Effects of orthopaedic wear particles on osteoprogenitor cells.Biomaterials. 2006 Dec;27(36):6096-101. doi: 10.1016/j.biomaterials.2006.08.023. Epub 2006 Sep 1. Biomaterials. 2006. PMID: 16949151 Review.
-
Wear debris in cemented total hip arthroplasty.Orthopedics. 1991 Mar;14(3):335-40. Orthopedics. 1991. PMID: 2020632 Review.
Cited by
-
Porous titanium particles for acetabular reconstruction in total hip replacement show extensive bony armoring after 15 weeks. A loaded in vivo study in 10 goats.Acta Orthop. 2014 Dec;85(6):600-8. doi: 10.3109/17453674.2014.960660. Epub 2014 Sep 19. Acta Orthop. 2014. PMID: 25238431 Free PMC article.
-
Aucubin suppresses Titanium particles‑mediated apoptosis of MC3T3‑E1 cells and facilitates osteogenesis by affecting the BMP2/Smads/RunX2 signaling pathway.Mol Med Rep. 2018 Sep;18(3):2561-2570. doi: 10.3892/mmr.2018.9286. Epub 2018 Jul 16. Mol Med Rep. 2018. PMID: 30015916 Free PMC article.
-
Actin and ERK1/2-CEBPβ signaling mediates phagocytosis-induced innate immune response of osteoprogenitor cells.Biomaterials. 2011 Dec;32(35):9197-206. doi: 10.1016/j.biomaterials.2011.08.059. Epub 2011 Sep 6. Biomaterials. 2011. PMID: 21899882 Free PMC article.
-
Proposal for a histopathological consensus classification of the periprosthetic interface membrane.J Clin Pathol. 2006 Jun;59(6):591-7. doi: 10.1136/jcp.2005.027458. J Clin Pathol. 2006. PMID: 16731601 Free PMC article.
-
Significance of nano- and microtopography for cell-surface interactions in orthopaedic implants.J Biomed Biotechnol. 2007;2007(8):69036. doi: 10.1155/2007/69036. J Biomed Biotechnol. 2007. PMID: 18274618 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources